Special Helmholtz Workshop — Heidelberg Heart II
German Cancer Research Center, Heidelberg, Germany
9–11 September 2011
Cell and Molecular Biology of the Junctions and their Functions in Heart Tissues —
When Cardiology meets Molecular Biology
Organizers: Walter Birchmeier, Werner W. Franke
Speakers
Cristina Basso (Padua, Italy) - A 15
Joyce Bischoff (Boston, USA) - A 38
Orest W. Blaschuk (Montreal, Canada) - A 27
Patrice Bouvagnet (Lyon, France) - A 20
Jonathan T. Butcher (Ithaca, USA) - A 37
Hugh M. Calkins (Baltimore, USA) - A 24
Yassemi Capetanaki (Athens, Greece) - A 8
Adrian H. Chester (Harefield, UK) - A 36
Elisabeth Ehler (London, UK) - A 5
Bernd K. Fleischmann (Bonn, Germany) - A 9
Norbert Frey (Kiel, Germany) - A 4
Michael H. Gollob (Ottawa, Canada) - A 19
Robert G. Gourdie (Charleston, USA) - A 6
Kathleen J. Green (Chicago, USA) - A 1
Axel Haverich (Hannover, Germany) - A 35
David P. Kelsell (London, UK) - A 33
Paulus Kirchhof (Münster, Germany) - A 21
Peter Kohl (Harefield, UK) - A 29
Calum A. MacRae (Boston, USA) - A 23
Roger R. Markwald (Charleston, USA) - A 31
Takashi Mikawa (San Francisco, USA) - A 10
Antoon F. M. Moorman (Amsterdam, The Netherlands) - A 11
John J. Mullins (Edinburgh, UK) - A 25
Sebastian Pieperhoff (Edinburgh, UK) - A 12
Laurentiu M. Popescu (Bucharest, Romania) - A 30
Karen E. Porter (Leeds, UK) - A 28
Nikos Protonotarios (Naxos, Greece) - A 18
Glenn L. Radice (Philadelphia, USA) - A 3
Steffen Rickelt (Heidelberg, Germany) - A 26
Mark W. Russell (Ann Arbor, USA) - A 7
Jeffrey E. Saffitz (Boston, USA) - A 16
Maya Simionescu (Bucharest, Romania) - A 13
Gaetano Thiene (Padua, Italy) - A 22
Adalena Tsatsopoulou (Naxos, Greece) - A 18
Jolanda van Hengel (Ghent, Belgium) - A 2
J. Peter van Tintelen (Groningen, The Netherlands) - A 14
Sir Magdi H. Yacoub (Harefield, UK) - A 34
Katherine E. Yutzey (Cincinnati, USA) - A 32
Abstracts of oral presentations
A 1 — Desmosomal molecules in and out of junctions
Kathleen J. Green, Adi Dubash, Lisa M. Godsel
Departments of Pathology and Dermatology, Northwestern University Feinberg School
of Medicine, Chicago, IL, USA
kgreen@northwestern.edu
Desmosomes are intercellular junctions that anchor the intermediate filament (IF)
cytoskeleton to sites of strong intercellular adhesion, and play a critical role in
ensuring mechanical integrity of the skin and the heart. Desmosome building blocks
come primarily from three protein families. Transmembrane members of the cadherin
family, the desmogleins and desmocollins, cooperate to form the adhesive interface.
Within the junctional plaque, the cytoplasmic tails of the cadherins provide a scaffold
for armadillo family members including plakoglobin and plakophilins (PKPs) 1-3 and
the IF-binding protein, desmoplakin (DP), which in turn anchors the strain-bearing
IF cytoskeleton to the plaque. In cardiac muscle, desmosome molecules are major architectural
components of the intercalated discs, highly organized regions of the plasma membrane
comprising components of adherens junctions, gap junctions, and desmosomes that together
coordinate mechanical and electrochemical signaling between adjacent cardiac myocytes.
In vertebrates, postnatal remodeling of these specialized regions of the plasma membrane
occurs, giving rise to the area composita in which desmosomal building blocks are
intermixed with components of adherens junctions.
The crucial functions of desmosome molecules in epithelial and cardiac tissues are
highlighted by the discovery of mutations that cause skin and heart disease. While
interference with the architectural roles of desmosome molecules has been assumed
to make an important contribution to tissue responses that lead to disease pathogenesis,
functions that transcend their well-established roles in adhesion and IF-anchorage
are emerging. Desmosome molecules have recently been shown to guide the remodeling
of microtubules during epidermal morphogenesis, and also govern actin remodeling by
regulating Rho GTPases during junction assembly.
Of particular interest is the desmosomal armadillo protein plakophilin 2 (PKP2), which
is reported as the most frequent target for mutation in arrhythmogenic right ventricular
cardiomyopathy (ARVC), a leading cause of sudden cardiac death in the young. We previously
showed that in epithelial cells, PKP2 regulates the localization and activity of RhoA
to locally control actomyosin contractile signaling important for cell junction formation,
while keeping global RhoA signaling in check. In the heart, signaling through RhoA
and its downstream effectors is critical for normal cardiac development and physiology.
Indeed, our data show that PKP2 silencing results in elevated RhoA and disruption
of actin organization in cardiac myocytes. Further, loss of PKP2 or its fellow armadillo
protein plakoglobin leads to elevated expression of target genes of the transcriptional
regulator SRF (serum response factor), which is activated in a RhoA-dependent fashion,
and along with Rho plays essential roles in cardiac development, hypertrophy and fibrosis.
These data suggest a new cellular pathway through which desmosome deficiency could
contribute to pathogenesis in ARVC.
A 2 — Alpha-catenins: emerging targets for diseases
Jolanda van Hengel
1, Jifen Li2, Steven Goossens1, Erhe Gao2, Lan Cheng2, Koen Tyberghein1, Xiying Shang2,
Riet De Rycke1, Frans van Roy1, and Glenn L. Radice2
(1) Department for Molecular Biomedical Research, Flanders Interuniversity Institute
for Biotechnology (VIB) and Ghent University, B-9052, Ghent, Belgium
(2) Center for Translational Medicine, Department of Medicine, Thomas Jefferson University,
Philadelphia, PA, USA
Jolanda.vanhengel@dmbr.vib-ugent.be
The adherens junction (AJ) is a type of cell–cell junction that develops near the
apical surface of polarized epithelial cells. Together with a bundle of cortical actin
filaments, the AJ is organized as a molecular belt. The AJ comprises cadherins, catenins,
and other associated proteins. Cadherins interact homophilically via their extracellular
domain, and physically link the adjacent cell membranes. The cytoplasmic region of
classic cadherins binds β-catenin, which in turn associates with α-catenin. Alpha-catenin
is indispensable for cadherin-mediated cell adhesion. In the absence of α-catenin,
the AJ is disrupted, and the apical actin belt dissociates from the cadherin–catenin
complex. It was commonly believed that the cadherin–catenin complex is physically
linked to actin fibers via α-catenin, and that this linkage is crucial for maintenance
of the AJ. However, this model has been challenged by the recently revealed inability
of the reconstructed cadherin–catenin complex to directly bind actin filaments in
vitro (Drees et al. 2005; Yamada et al. 2005). However, a number of mechanisms can
be proposed to reconcile these observations. One possibility is that additional mediators
serve as a bridge between the cadherin-bound α-catenin and F-actin. Three homologous
α-catenin proteins are known: the ubiquitously expressed αE-catenin, the neurally
expressed αN-catenin, and αT-catenin with a restricted expression pattern. AlphaT-catenin
is especially abundant in heart tissue, where it is co-expressed with αE-catenin in
areae compositae, which are present at the intercalated discs (ICD). In vitro, αN-
and αT-catenin can substitute for the adhesive functions of αE-catenin, but their
restricted expression patterns in vivo indicate that they have tissue-specific functions.
This hypothesis was confirmed by the inability of endogenous αT-catenin expression
to rescue a heart-specific αE-catenin knock-out in mice (Sheikh et al. 2006). We have
shown that αT-catenin has the following isoform-specific function: it interacts specifically
with plakophilins (PKP), whereas αE- and αN-catenin cannot (Goossens et al. 2007).
To investigate the function of alphaT-catenin, we generated a loss-of-function model
in mouse. AlphaT-catenin-null mice are viable, but they exhibit progressive cardiomyopathy
(Li et al. 2011). We observed reduced expression of PKP-2 in the ICD of αT-catenin-null
myocardium. Furthermore, Cx43 was reduced at the ICD, including its co-localization
with N-cadherin. This finding suggests that αT-catenin may function synergistically
with desmosomal PKP-2 to stabilize gap junctions at the area composita. This gap junction
remodeling was associated with an increased incidence of ventricular arrhythmias in
αT-catenin-null mice when subjected to acute ischemia.
Drees F, Pokutta S, Yamada S, Nelson WJ, Weis WI (2005) α-Catenin is a molecular switch
that binds E-cadherin-β-catenin and regulates actin-filament assembly. Cell 123:903–915
Goossens S, Janssens B, Bonné S, De Rycke R, Braet F., van Hengel J, van Roy F (2007)
A unique and specific interaction between αT-catenin and plakophilin-2 in the area
composita, the mixed-type junctional structure of cardiac intercalated discs. J Cell
Sci 120:2126–2136
Li J, Goossens S, van Hengel J, Gao E, Cheng L, Tyberghein K, Shang X, De Rycke R,
van Roy F, Radice GL (2012) Loss of alphaT-catenin alters the hybrid adhering junctions
in the heart and leads to dilated cardiomyopathy and ventricular arrhythmia following
acute ischemia. J Cell Sci 125:1058–1067
Sheikh F, Chen Y, Liang X, Hirschy A, Stenbit AE, Gu Y, Dalton ND, Yajima T, Lu Y,
Knowlton KU, Peterson KL, Perriard J-C, Chen J (2006) α-E-catenin inactivation disrupts
the cardiomycyte adherens junction, resulting in cardiomyopathy and susceptibility
to wall rupture. Circulation 114:1046–1055
Yamada S, Pokutta S, Drees, F, Weis WI, Nelson WJ (2005) Deconstructing the cadherin-catenin-actin
complex. Cell 123:889–901
A 3 — Catenins: multi-function proteins involved in cell adhesion, communication,
and signaling in the heart
Jifen Li1, David Swope1, Lan Cheng1, Erhe Gao1, Natalia Raess2, Eliane J. Müller2,
Jolanda van Hengel3, Frans van Roy3, Glenn L. Radice
1
(1) Center for Translational Medicine, Department of Medicine, Thomas Jefferson University,
Philadelphia, PA, USA
(2) Molecular Dermatology, Institute of Animal Pathology, University of Bern, Bern,
Switzerland
(3) Department of Molecular Biomedical Research, Flanders Interuniversity Institute
for Biotechnology (VIB)-Ghent University, B-9052, Ghent, Belgium
Glenn.Radice@jefferson.edu
Efficient cardiac contractile function is highly dependent upon the coordinated mechanical
and electrical activation of the myocardial tissue. Many of the molecular components
required for mechano-electrical coupling in the heart are localized at the end-to-end
connection between myocytes called the intercalated disc (ID). The ID consists of
three main junctional complexes: adherens junctions and desmosomes provide strong
cell–cell adhesion, and gap junctions provide electrical coupling between the myocytes.
ID structure is dependent on N-cadherin, the only classical cadherin expressed in
the myocardium (Kostetskii et al. 2005). Cadherin-mediated adhesion requires interaction
with the actin cytoskeleton via a family of proteins called catenins. Whether the
different catenin subtypes have distinct or synergistic functions in the heart is
not clear.
Mutations in γ-catenin (also known as plakoglobin) are associated with arrhythmic
right ventricular cardiomyopathy (ARVC), a hereditary heart-muscle disease that causes
sudden cardiac death (SCD) in young people. To investigate the role of PG in ARVC,
we generated a cardiac-specific knockout (CKO) of the plakoglobin (JUP) gene in mice
(Li et al. 2011). Interestingly, despite gap junction remodeling, PG CKO mice have
no apparent conduction abnormality and survive longer than expected. Importantly,
the PG homolog, β-catenin, showed increased association with the gap junction protein,
connexin43 (Cx43) in PG CKO hearts. To determine whether β-catenin protects PG CKO
animals from sudden arrhythmic death, we generated mice lacking both PG and β-catenin
specifically in the heart (i.e., double knockout, DKO). The PG/β-catenin DKO mice
exhibited acute cardiomyopathy, fibrous tissue replacement, and conduction abnormalities
resulting in SCD 3–5 months after deleting both genes. In contrast to the PG and β-catenin
single mutants, N-cadherin was significantly reduced at the ID in the PG/β-catenin
DKO mice. Moreover, the ID structure was disrupted in the PG/β-catenin DKO hearts,
consistent with the loss of adherens junction and desmosome proteins from the ID.
Collectively, our results demonstrate that PG is more important for the structural
integrity of the heart than β-catenin; however, β-catenin maintains gap junctions
in the absence of PG, indicating that these proteins cooperate to maintain electrical
coupling in the heart.
There are two α-catenin subtypes expressed in the myocardium, αE-catenin and αT-catenin;
together, they are thought to modulate interactions between N-cadherin/catenin complex
and the actin cytoskeleton. A novel αT-catenin KO mouse model demonstrates for the
first time how perturbation in αT-catenin can affect both PKP-2 and Cx43, thus highlighting
the importance of understanding the cross-talk between the junctional proteins of
the area composita and its implications for arrhythmogenesis (Li et al. 2012).
Kostetskii I, Li J, Xiong Y, Zhou R, Ferrari VA, Patel VV, Molkentin JD, Radice GL
(2005) Induced deletion of the N-cadherin gene in the heart leads to dissolution of
the intercalated disc structure. Circ Res 96:346–354
Li J, Swope D, Raess N, Cheng L, Muller EJ, Radice GL (2011) Cardiac tissue-restricted
deletion of plakoglobin results in progressive cardiomyopathy and activation of β-catenin
signaling. Mol Cell Biol 31:1134–1144
Li J, Goossens S, van Hengel J, Gao E, Cheng L, Tyberghein K, Shang X, De Rycke R,
van Roy F, Radice GL (2012) Loss of alphaT-catenin alters the hybrid adhering junctions
in the heart and leads to dilated cardiomyopathy and ventricular arrhythmia following
acute ischemia. J Cell Sci 125:1058–1067
A 4 — Transgenic overexpression of the intercalated disc protein myozap causes protein
aggregate-associated cardiomyopathy
Derk Frank1, Thalia S. Seeger2, Claudia Rohr2, Christian Kuhn1, Christine Grund3,
Rainer Will2, Werner W. Franke3, Hugo A. Katus2, Norbert Frey
1
(1) Dept. of Cardiology and Angiology, UK-SH, Kiel, Germany
(2) Dept. of Internal Medicine III, University of Heidelberg, Germany
(3) Helmholtz Group Cell Biology, DKFZ, Heidelberg, Germany
Norbert.Frey@uk-sh.de
The intercalated disc (ID) is an important component of the cell–cell contact structures
of cardiomyocytes. During the last decade, it became evident that the molecular components
of the ID are critical regulators in the pathogenesis of inherited cardiac disease
(van Tintelen et al. 2007). We were able recently to identify and characterize a novel
cardiac-enriched ID protein, termed myozap. It interacts with several other ID proteins
including desmoplakin.
Mechanistically, it represents a positive modulator of the Rho-dependent SRF pathway
linking the ID to gene regulation processes and actin dynamics (Seeger et al. 2010).
To further insight in myozap’s function in vivo, we generated a mouse model with cardiac-restricted
overexpression of myozap cDNA using the αMHC promoter. These mice developed substantial
cardiac hypertrophy (heart weight/tibia length +43 %, p < 0.01, n = 8–10) as well
as progressive LV dilation (LVEDD +20 %, p < 0.01). Consistently, myozap-transgenic
hearts displayed upregulation of the hypertrophy-associated “fetal” gene program (e.g.,
ANF 4.3-fold, p < 0.001, and BNP 2.2-fold, p < 0.01, n = 7–9). Next, myozap transgenic
animals were subjected to various forms of stress, including voluntary running wheel
exercise, which led to an accelerated cardiomyopathy with premature LV dysfunction
and dilation. Moreover, chronic infusion of the alpha-agonist phenylephrine (PE) caused
significant lethality in myozap-Tg [n = 5/8, p < 0.05 vs WT (1/7)]. Unexpectedly,
on the ultrastructural level, we were able to detect bulky protein aggregates containing
myozap, desmoplakin, and other ID proteins. This aggregate-associated pathology closely
resembled the changes in the hearts of patients suffering from desminopathies (Goldfarb
and Dalakas 2009). It should be noted that desmin was not detectable in the aggregates
of myozap tansgenic mice, but was displaced from the ID.
Taken together, cardiac overexpression of the novel ID protein myozap leads to hypertrophy
and dilated cardiomyopathy, accompanied by protein aggregates and associated with
sudden death upon PE treatment. Further analyses of this transgenic model may help
to understand the pathogenesis and pathophysiology of protein aggregate-associated
cardiomyopathies.
Goldfarb LG, Dalakas MC. (2009) Tragedy in a heartbeat: malfunctioning desmin causes
skeletal and cardiac muscle disease. J Clin Invest 119:1806–1813
Seeger TS, Frank D, Rohr C, Will R, Just S, Grund C, Lyon R, Luedde M, Koegl M, Sheikh
F, Rottbauer W, Franke WW, Katus HA, Olson EN, Frey N (2010) Myozap, a novel intercalated
disc protein, activates serum response factor-dependent signaling and is required
to maintain cardiac function in vivo. Circ Res 106:880–890
van Tintelen JP, Hofstra RM, Wiesfeld AC, van den Berg MP, Hauer RN, Jongbloed JD.
(2007) Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging
horizon? Curr Opin Cardiol 22:185–192
A 5 — The intercalated disc — a truly special type of cell-cell contact in dilated
cardiomyopathy
Alain Hirschy, Elisabeth Ehler
King’s College London BHF Research Excellence Centre, The Randall Division of Cell
and Molecular Biophysics and The Cardiovascular Division, New Hunt’s House, Guy’s
Campus, London SE1 1UL, United Kingdom
elisabeth.ehler@kcl.ac.uk
Two multiprotein complexes are essential for proper functioning of the heart: the
myofibrils are responsible for carrying out the contractile work, and the intercalated
disc, a specialised type of cell–cell contact, is indispensable for proper mechanical
and electrochemical contact between the individual cardiomyocytes. Both structures
are characterized by their extremely regular arrangement, which in case of the intercalated
disc is only achieved after birth. We have shown previously that alterations in intercalated
disc composition are a hallmark of dilated cardiomyopathy (DCM) in mice and men (Ehler
et al., 2001). There is an upregulation of expression of proteins that are involved
in the anchoring of actin filaments accompanied by an increased convolution of the
plasma membrane. This probably leads to an overall stiffening of the cell–cell contacts.
In the rodent DCM heart, there is also a reduction in the expression of gap junction
proteins, which is expected to lead to decreased intercellular communication. Since
stoichiometry is clearly important for proper function, we have decided to challenge
it by gain and loss of function experiments, targeting the adherens junction protein
beta-catenin.
In our system, the postnatal loss of beta-catenin in cardiomyocytes has comparatively
little effect on heart function; however, when we overexpress beta-catenin in the
heart we observe a dramatic phenotype of DCM, with all the mice dead by 5 months of
age (Hirschy et al., 2010). Interestingly, despite an excess of beta-catenin per targeted
cell, we never observed any beta-catenin in the nucleus of postnatal cardiomyocytes.
We conclude that increased amounts of beta-catenin at the intercalated disc are not
tolerated by the heart, but that nuclear beta-catenin signaling is probably not very
relevant in the fully differentiated cardiomyocyte.
Ehler E, Horowits R, Zuppinger C, Price RL, Perriard E, Leu M, Caroni P, Sussman M,
Perriard J-C (2001) Alterations at the intercalated disk associated with the absence
of muscle LIM protein. J. Cell Biol 153:763–772
Hirschy A, Croquelois A, Perriard E, Schoenauer R, Agarkova I, Hoerstrup SP, Taketo
MM, Pedrazzini T, Perriard J-C, Ehler D (2010) Stabilised beta-catenin in postnatal
ventricular myocardium leads to dilated cardiomyopathy and premature death. Basic
Res Cardiol 105:597–608
A 6 — The connexin carboxyl terminus and cardiac gap junction organization
Robert G. Gourdie
Department of Regenerative Medicine and Cell Biology and Clemson-MUSC Bioengineering
Program, Medical University of South Carolina, Charleston, SC, USA
gourdier@musc.edu
The precise spatial order of gap junctions at intercalated disks in adult ventricular
myocardium is thought vital for maintaining cardiac synchrony. Breakdown or remodeling
of this order is a hallmark of arrhythmic disease of the heart. The principal component
of gap junction (GJ) channels between ventricular cardiomyocytes is connexin43 (Cx43).
Protein–protein interactions and modifications of the carboxyl-terminus (CT) of Cx43
are key determinants of GJ function, size, distribution, and organization during normal
development and in disease processes. This talk will focus on the work of my lab on
protein interactions at the Cx43 CT in the regulation of GJ organization. There will
be a particular emphasis on the role of the protein Zonula Occludens-1 (ZO-1). Topics
covered will include our recent identification of the perinexus — a novel, hemichannel-containing
domain surrounding the GJ that is enriched for Cx43-ZO-1 interaction.
Our recent studies of the mode-of-action of a peptide based on the Cx43 CT that inhibits
GJ remodeling at injury border zone (IBZ) and reduces inducible arrhythmias following
cryo-infarction of the left ventricle will be presented. Also discussed will be preliminary
data on potential assignments of the Cx43 CT in myocyte–fibroblast interaction at
the IBZ and ZO-1 interaction with Cx40 and Cx45 — connexins expressed in the conduction
system.
A 7 — Outside-in and inside-out signaling through cell–cell and cell–matrix adhesion
complexes promotes myofibril organization in striated muscle
Mark W. Russell
Division of Pediatric Cardiology, Department of Pediatrics and Communicable Dieases,
University of Michigan, Ann Arbor, MI, USA
mruss@med.umich.edu
During development, cardiac and skeletal myoblasts differentiate into myocytes and
skeletal myotubes with mature contractile structures that are precisely oriented with
respect to surrounding cells and tissues. Establishment of this highly ordered structure
requires coordinate and reciprocal interactions between the differentiating myocytes
and the extracellular environment, including neighboring cells and the surrounding
extracellular matrix. “Outside-in” signals from the extracellular environment result
in changes to myocyte morphology, and promote new myofibril assembly; in return, “inside-out”
signals pattern adjoining cells and the extracellular matrix, and coordinate the assembly
and organization of myofibrils across cells and tissues. Communication between the
cell and extracellular environment is mediated by transmembrane adhesion complexes,
the composition and complexity of which depend on the cell type and degree of differentiation.
In cardiac myocytes, axial connections occur at intercalated disks in which desmosomes
(maculae adhaerentes), fasciae adhaerentes, and gap junctions form mechanical and
electrochemical communications between adjacent cells. Examination of remodeling adult
rat cardiac myocytes in primary culture suggests that outside-in signals from surrounding
cells establish a well-defined axis of contraction, resulting in cytoskeletal remodeling
and reorganization of the myofibrils. Inside-out signals restrict the adhesive contacts
to the termini of the reorganized myofibrils, supporting the layered addition of armadillo
family proteins and cytoskeletal adaptors to the cadherin- and desmosomal cadherin--based
adhesive contact. A similar process occurs at integrin-based adhesion contacts within
the costameres of cardiac and skeletal muscle. At those sites, outside-in and inside-out
signals transmitted through the adhesion complexes promoted organization of the internal
structure of the myocyte and translation of those structural cues to surrounding cells
and tissues. Our findings support a model of myofibril assembly and organization as
a dynamic process involving the interaction of intracellular compartments with specialized
transmembrane adhesion domains. Identification of the linking elements that promote
the coordinated remodeling of the sarcomere and cell–cell and cell–matrix contacts
will be essential in developing strategies to prevent muscle injury and promote muscle
repair in patients with cardiac and skeletal myopathies and muscular dystrophies.
A 8 — Desmin as a major player in heart failure and a potential link between ARVD/C
and DCM
Yassemi Capetanaki
Division of Cell Biology, Center of Basic Research I, Biomedical Research Foundation,
Academy of Athens, Athens, Greece
ycapetanaki@bioacademy.gr
It has been demonstrated that gene inactivation in mice or mutations in humans in
the major intermediate filament protein desmin leads to all forms of cardiomyopathy
(DCM, HCM, RCM, ARVD/C) and eventually heart failure. Desmin forms a continuous network
connecting the contractile apparatus to the sarcolemma (costameres & intercalated
discs), nucleus, and several membranous organelles. Mutations in proteins that associate
to the desmin network directly or indirectly also lead to cardiomyopathy. Importantly,
the type of developed cardiomyopathy depends on the cardiomyocyte structure at which
the desmin network-associated proteins are localized. Thus, costameric proteins such
as dystrophin, α-dystroglycan, and δ-sarcoglycan, nuclear proteins such as the nuclear
intermediate filament protein lamin A/C, and different lamin-associated proteins,
such as LAP2alpha and emerin, and finally, at the Z-disc region, proteins such as
plectin and the chaperon protein αB-crystallin, are associated to DCM. On the other
hand, mutations in genes encoding several proteins of the area composita (Franke et
al. 2007) of the intercalated disc, such as desmoplakin, plakoglobin, plakophilin
2, desmoglein 2, and desmocollin, have been identified as the genetic basis of ARVD/C.
Interestingly, preliminary genotype–phenotype assessment indicates that mutations
affecting the outer dense plaque of the desmosome result in ARVD/C, while mutations
at the inner dense plaque, particularly affecting the desmin-binding site of desmoplakin,
result in ARVD/C with left ventricular involvement and extensive overlap with DCM.
Similarly, the S13F desmin mutation, identified recently in patients with ARVD/C (Van
Spaendonck-Zwarts et al. 2011), is the most upstream mutation of the desmin head domain
found so far, and the observation that this mutation results in abnormalities at the
intercalated disc region, potentially by disruption of desmin-desmoplakin association,
is important and could allow the molecular understanding of the transition from mainly
ARVD/C to ARVDC/DCM and to mainly DCM development.
The most common desmin-related heart disease is the TNF- α linked heart failure. We
have demonstrated that activation of caspases by cytokines, such as TNF-α, known to
cause heart failure, leads to desmin cleavage and aggregate formation, loss of desmin
and other proteins (at least β-catenin and desmoplakin) from intercalated discs (IDs),
destabilization of IDs, mitochondrial defects, and heart failure. Strikingly, we have
found that when the WT desmin is replaced by a caspase-resistant desmin (D263E), in
TNF-α over-expressing mouse heart, these pathological features are greatly ameliorated,
demonstrating that desmin is a major target and plays a crucial role in the development
of the TNF-α-induced heart pathology (Panagopoulou et al. 2008). As our studies have
demonstrated (reviewed by Capetanaki et al. 2007), the desmin null heart failure model
possesses a combination of the pathophysiology of most types of cardiomyopathy, particularly
DCM and ARVD/C (characterized by cell death, extensive inflammation, fibrosis, and
degeneration, in both right and left ventricle, followed by systolic dysfunction and
conduction system defects). Therefore, we use this model for several studies aimed
to both unravel the mechanism of cardiomyopathy and heart failure development, as
well as to develop therapeutic strategies for the disease. The successes towards these
goals, and specifically the rescue of the desmin deficient heart failure by αB-cystallin
overexpression, will be discussed.
Capetanaki Y, Bloch RJ, Kouloumenta A, Mavroidis M,Psarras S (2007) Muscle intermediate
filaments and their links to membranes and membranous organelles. Exp Cell Res 313:2063–2076
Franke WW, Schumacher H, Borrmann CM, Grund C, Winter-Simanowski S, Schlechter T,
Pieperhoff S, Hofmann I (2007) The area composita of adhering junctions connecting
heart muscle cells of vertebrates - III: assembly and disintegration of intercalated
disks in rat cardiomyocytes growing in culture. Eur J Cell Biol. 86:127–142
Panagopoulou P , Davos C, Milner D, Varela E, J, Mann D, Capetanaki Y (2008) Desmin
mediates TNF-a induced aggregate formation and intercalated disk reorganization in
heart failure. J Cell Biol 181:761–775
Van Spaendonck-Zwarts KY, van Hessem L, Jongbloed JDH, Hermien EK, de Walle HEK, Capetanaki
Y, van der Kooi AJ, van Langen IM, van den Berg MP, van Tintelen JP (2011) Desmin
related myopathy: a review and meta-analysis. Clin Genet 80:354–366
A 9 — Potential and pitfalls of cellular replacement approaches in the heart
Bernd K. Fleischmann
Institute of Physiology I, Life & Brain Center, University of Bonn, Germany
bernd.fleischmann@uni-bonn.de
Myocardial infarction is characterized by an irreversible loss of cardiomyocytes and
scar formation, often resulting in heart failure. The only causal treatment currently
available is heart transplantation. However, due to shortage of donor organs, cell
replacement using progenitors and/or stem cells is considered a promising alternative
approach. We have explored the plasticity of these cells to differentiate into cardiac
muscle, their physiological integration and contribution to pump function in vivo.
Heart infarctions (cryoinjury, LAD ligation) were induced in mouse and progenitors/stem
cells mobilized with cytokines or directly injected into the infarct area. We have
first assessed the plasticity of bone marrow (BM)-derived cells. These neither differentiated
into functional cardiac muscle or endothelial cells, nor strongly enhanced left ventricular
function. Similar results were obtained when using BM-derived mesenchymal stem cells.
Importantly, their differentiation was not restricted by the heart tissue, as calcifications
and bone formation could frequently be observed. In contrast, fetal cardiomyocytes
stably engrafted into the infarct, and enhanced left ventricular function. Furthermore,
the engrafted cardiac muscle cells functionally integrated into the cardiac and strongly
reduced post-infarct arrhythmias. This was related to increased conduction velocities
in areas containing the cellular grafts. We also analyzed the potential of embryonic
stem (ES) cell-derived cardiomyocytes for cell replacement therapy. An antibiotic-based
selection approach was used to obtain highly purified cardiomyocytes and to avoid
teratoma formation due to contaminating pluripotent ES cells.
Transplantation experiments revealed that co-injection of purified cardiomyocytes
and fibroblasts increased the degree of engraftment, and resulted in an improvement
of left ventricular function. Thus, cardiac progenitors and ES cell-derived cardiomyocytes
stably engraft into the infarcted myocardium and enhance heart function.
A 10 — Cellular and molecular aspects of early heart formation
Takashi Mikawa, Michael Bressan
Cardiovascular Research Institute, University of California, San Francisco, CA, USA
takashi.mikawa@ucsf.edu
Complex organization of the heart is established through the orchestrated and sequential
processes of commitment, proliferation, and movements of multiple cell types. A spatiotemporally
regulated binary decision model was once considered the major mechanism for generating
multiple cardiac cells from a common stem cell population. This model was used to
describe the genesis of myocyte vs endocardial endothelial cell lineages and atrial
vs ventricular myocyte lineages, as well as coronary endothelial vs smooth muscle
lineages. Contrary to this idea, mounting evidence collected in recent years indicates
that lineage segregation of individual cardiac cell types actually occurs prior to
arrival of their progenitors to the heart. The resolution of these two models lies
at the core of many controversies in cardiovascular developmental biology. They need
not be mutually exclusive, however. For instance, differing components of the cardiac
conduction system rely on both predetermination of separate cell population and diversification
of fate from common precursors. We have shown that the induction and patterning of
the fast-conducting Purkinje fiber network, which is mediated by hemodynamic-activated
paracrine cues, involves the recruitment of already beating ventricular myocytes into
the Purkinje fiber lineage. Conversely, our recent data suggest that prior to heart
tube formation the pacemaker cell lineage of the sinoatrial node is specified in a
mesoderm population that is separate from precursors of other cardiac cell types.
Our cell lineage studies in chick embryos have also demonstrated that the segregation
as well as differentiation of coronary smooth muscle, fibroblast, and endothelial
cell lineages begins in an extracardiac tissue, the proepicardium, prior to their
entry to the heart. A separate origin of coronary smooth muscle and endothelial cell
lineages have been confirmed by recent genetic studies of mouse embryos. Thus, a precisely
timed sequence of development and integration of individual cardiac sub-components
is mediated through multiple genetic and epigenetic programming during heart formation
in higher vertebrates.
[Supported in part by grants from NIH-NHLBI.]
A 11 — Development of the building plan of the heart
Antoon F.M. Moorman
Department of Anatomy, Embryology & Physiology, Academic Medical Centre, Amsterdam,
The Netherlands
a.f.moorman@amc.uva.nl
One of the most fascinating aspects in the formation of the heart is the very early
development of the electrical patterning as can be registered by the ECG, which is
the registration of the rhythmic waves of depolarizing activity over the cardiac muscle.
In the mature heart, the conduction system is held responsible for the rhythmic excitations
and contractions. However, in chicken embryos a sinusoidal type of ECG can already
be derived from the linear heart tube stages at about 2 days of development onward;
and less than 1 day later, when chamber formation has just been initiated, an adult
type of ECG can be monitored. The presence of an adult type of ECG in these early
embryonic hearts betrays the development of fast-conducting chambers rather than the
presence of a conduction system. We now know that the primary heart tube as seen in
the early embryo contains the precursors for the left ventricle only, or even less,
whereas the precursor cells for the remainder of the cardiac components are continuously
added to both the venous and arterial pole of the heart tube during further development
from a single center of growth outside the heart. Therefore, it is impossible that
the straight heart tube contains the precursors for the conduction system as rings
separating the purported cardiac segments. While the primary heart tube is growing
by addition of cells, it does not show significant cell proliferation until chamber
differentiation and expansion starts locally in the tube. The transcriptional repressors
Tbx2 and Tbx3 locally repress the chamber-specific program of gene expression, by
which these regions are allowed to differentiate into the distinct components of the
conduction system. The cardiac building plan and the underlying mechanisms of its
formation are conserved from fish to man.
Detailed reconstructions of the developmental patterns of expression of Tbx3 during
development in mouse and human have revealed that Tbx3 is expressed in those areas
of the heart tube that do not become chamber, i.e., in the sinu-nodal region, internodal
region, atrioventricular junction, atrioventricular bundle, and bundle branches. These
areas comprise not only the conventional conduction system, but also the highly controversial
areas of the internodal region and the entire atrioventricular junction. Also the
(right) ventricular outflow tract initially expresses these transcriptional repressors,
preventing it from chamber differentiation. These observations provide an embryonic
basis for why some areas in the heart are more arrhythmogenic than other regions.
Christoffels VM Moorman AFM (2009) Development of the cardiac conduction system: Why
are some regions of the heart more arrhythmogenic than others? Circulation 2:195–207
Moorman AFM, Christoffels VM (2003) Cardiac chamber formation: development, genes,
and evolution. Physiol Rev 83:1223–1267
Sizarov A, Ya J, PhD, de Boer BA; Lamers WH, Christoffels VM, Moorman AFM (2011) Formation
of the building plan of the human heart: morphogenesis, growth, and differentiation.
Circulation 123:1125–1135
van den Berg G, Abu-Issa R, de Boer BA, Hutson MR, de Boer PAJ, Soufan AT, Ruijter
JM, Kirby ML, van den Hoff MJB, Moorman AFM (2009) A caudal proliferating growth center
contributes to both poles of the forming heart tube. Circ Res 104:179–188 (On-line
interactive 3D PDF file available)
A 12 — Modulations of cardiomyocyte adhering junctions during embryonic development
and evolution
Sebastian Pieperhoff
Centre for Cardiovascular Science, Queen's Medical Research Institute, University
of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, Scotland, UK
S.Pieperhoff@gmail.com
A detailed reinvestigation of adult mammalian cardiomyocyte adhering junctions resulted
in the discovery and definition of the composite junction (area composita). The chosen
terminology highlights the hybrid character of adhering junctions connecting adult
mammalian cardiomyocytes, which are composed of typical desmosomal as well as adherens
junction components. Therefore, desmosomal proteins are not restricted to relatively
small desmosomes (as in various epithelia), but are localized within the entire cardiac
intercalated disks.
Obviously, desmosomal proteins serve their function also in adhering junctions anchoring
myofibrillar actin bundles, the composite junctions. This is of particular interest,
as single mutations in genes encoding for such desmosomal proteins have been linked
to the development of inherited forms of cardiomyopathies, such as the arrhythmogenic
right ventricular cardiomyopathy/dysplasia (ARVC/D), often without any signs of cutaneous
disease involvement. In a subsequent series of studies, I was then able to show that
the formation of composite junctions is a rather late event in both, mammalian development
and vertebrate evolution. Nascent cardiomyocytes of early mammalian embryonic stages
are for the most part connected by relatively small intermediate filament binding
desmosomes and myofibrillar actin binding adherens junctions (quite similar to adhering
junctions connecting epithelial cells). During late heart development (after birth),
single components of both structures become more and more fused, and gradually relocated
at the two poles within the composite junctions of the mature mammalian ventricular
cardiomyocytes. Furthermore, results of studies on the adhering junctions connecting
cardiomyocytes of various lower vertebrate and invertebrate species will be briefly
presented. The findings described will be discussed in relation to cardiomyopathy
development and heart muscle regeneration.
A 13 — Endothelia of heart vessels: structure, molecules, functions and dysfunctions
Maya Simionescu
Institute of Cellular Biology and Pathology "Nicolae Simionescu", Bucharest, Romania
maya.simionescu@icbp.ro
The endothelial cell (EC) has earned the attention and respect of biologists, who
over the years discovered that far from being a gratuitous cellophane-like layer,
it has a key role in body homeostasis and a large variety of pathologies. Along the
cardiovascular system, the structure of the EC layer, which constitutes the boundary
between the blood and the tissues, varies as a function of the vessel or organ in
which they reside. The acquired innate heterogeneity consisting of the distribution/number
and organization of caveolae, channels, type of intercellular junctions, and the presence/absence
of fenestrae, confers to ECs the ability to adjust, sense, monitor, command, and modulate
particular local functions, as well as to respond to a variety of aggressive factors.
In physiological conditions, EC heart vessels (and in many other locations) have a
large array of constitutive functions and the proper molecular configuration to regulate
the bidirectional receptor-mediated and receptor-independent transcytosis of molecules
between the plasma and tissues, to execute endocytosis, to synthesize their own basal
lamina and extracellular matrix components, to guard vascular tone (by balanced synthesis
of vasoactive mediators PGI2, NO, EDHF, and endothelin), to regulate cellular cholesterol
and lipid homeostasis, and to administer haemostasis (via vWf and PAI-1), signal transduction,
and immunity. At the molecular level, many of these functions are implemented by EC
caveolae, which are structurally and functionally differentiated microdomains of the
plasmalemma endowed with receptors for LDL, HDL, albumin, transferrin, EGF, AGE, and
insulin, as well as death receptors (IL-1-R and P75-R).
Pathological conditions, i.e., exposure to cardiovascular risk factors (hyperlipemia/hyperglycemia),
lead to EC dysfunctions, a key event in all stages of vascular diseases such as atherosclerosis.
The ECs sense the variations occurring in the plasma or tissues, and initiate a focal
response (in arterial-susceptible areas) manifested firstly by adaptation/modulation
of their constitutive functions, such as increased transcytosis of β-lipoproteins
(βLp), and enhanced synthesis of basal lamina and extracellular matrix components.
The increased transcytosis and the reduced efflux from the intima, generate βLp alterations
(oxidation, glycation, enzymatic modifications) and retention within the ECs' hyperplasic
basal lamina as modified lipoproteins (mLp). The latter, together with modifications
of plasma homeostasis, induce EC dysfunction (novel adhesion molecules, secretion
of chemokines, cytokines), which triggers a robust inflammatory reaction (recruitment
and transvasation of immune cells within the intima). All these alterations contribute
to atheroma formation and development in the heart vessels, aorta, and other arterial
segments. Ultimately, the insults present inside and outside the vessel wall lead
to EC injury, apoptosis, and the ensuing vulnerable plaque rupture and atherothrombosis.
At the molecular level, the disease lies within the EC, since vascular aggressors
induce a cell organelle pathology manifested by amendments of membrane components
(new adhesion molecules), malfunction of caveolae, and alterations in regulated transcytosis,
and in the functions of the endoplasmic reticulum, Golgi complex (switch to a secretory
phenotype), lysosomes (enzyme failure), and opening of intercellular junctions. The
wealth of data on the role of ECs in health and disease may constitute together a
complex discipline that includes endotheliology, endotheliopathy, and endotheliotherapy.
[Work supported by grants from NIH-USA, European Community, Romanian Academy and Ministry
of Education and Research, Romania]
A 14 — Arrhythmogenic right ventricular cardiomyopathy; a clinical and genetic perspective
on desmosomes, desmin and calcium
J. Peter van Tintelen
Department of (Clinical) Genetics, University Medical Center Groningen, Groningen,
The Netherlands
p.van.tintelen@medgen.umcg.nl
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy
which usually presents with palpitations or syncope due to ventricular tachyarrhythmias.
These arrhythmias may also underlie sudden death at relatively young ages. The general
hallmark of this disease is (fibro-)fatty replacement of myocardial tissue, which
contributes to activation delay, reentry and subsequent ventricular tachycardia. The
areas of fibrofatty replacement are mainly localized in the right ventricle (RV).
The diagnosis of ARVC is made using generally accepted task force criteria. The initial
criteria published in 1994 excluded left ventricular (LV) involvement. However, in
recent years it has become clear that serious LV involvement can be found in ARVC
as well. Recently, more left-dominant forms of "ARVC" were observed (ALVC). Based
on these observations, the task force criteria for ARVC were recently modified to
improve diagnostic sensitivity while maintaining specificity. Therefore, quantitative
criteria were proposed. Besides, LV involvement is no longer an exclusion criterion,
while the identification of a pathogenic mutation for ARVC is incorporated in the
new criteria.
The elucidation of genes underlying ARVC started in 2000 with the discovery that autosomal
recessive Naxos disease — a cardiocutaneous syndrome with ARVC and skin and hair abnormalities
— was due to a deletion in the gene encoding plakoglobin. This is an important part
of the desmosome. This discovery paved the road for the discovery of genes underlying
autosomal dominantly inherited ARVC, such as plakophilin 2 (PKP2), desmoglein 2, desmocollin
2, and desmoplakin, all encoding proteins of the cardiac desmosome. Recently, desmin
was added to this list. Because of the clinical overlap between left sided "ARVC"
and dilated cardiomyopathy (DCM) a disease mainly involving the LV, we recently screened
the phospholamban gene (PLN), a calcium-handling gene, in large DCM and ARVC cohorts
from the Netherlands. This led to the identification of a previously described PLN
mutation (R14del) in 10–15% of patients in both groups. This mutation has previously
been described in DCM patients from other countries, and preliminary data show that
this might be a global founder mutation. Interestingly, myocardial biopsies in PLN
R14del ARVC patients show absent or reduced plakoglobin at the intercalated disk which
has been suggested to be specific for ARVC, while the PLN R14del DCM patients generally
show normal amounts of plakoglobin at the intercalated disk. These observations shift
the paradigm that ARVC is solely due to mutations in desmosomal genes. The majority
(>40 %) of ARVC patients carry mutations in PKP2. If we consider proven familial cases
of ARVC, PKP2 mutations can be identified in up to 70 % of families. This might suggest
highly penetrant disease; however, not all desmosomal gene mutation carriers develop
disease. This is also reflected by some recent large-scale population-based studies
from Finland and the United States. In these studies, 0.5 % of healthy controls carried
pathogenic mutations predisposing to ARVC, while the prevalence of ARVC is believed
to be 1:1000–1:5000. The non-penetrance, clinical variability, and high prevalence
of mutations in the general population hampers tailor-made therapy and surveillance
in mutation carriers, who have a chance of dying suddenly, even in the absence of
abnormalities in cardiological evaluation.
A 15 — The changing spectrum of arrhythmogenic cardiomyopathy
Cristina Basso
Department of Medico-Diagnostic Sciences and Special Therapies, University of Padua
Medical School, Padua, Italy
cristina.basso@unipd.it
Arrhythmogenic cardiomyopathy (AC) is a clinically and genetically heterogeneous heart
muscle disorder associated with ventricular arrhythmias and even risk of sudden death.
The disease is heredo-familial, and mutations in desmosomal genes (plakoglobin, desmoplakin,
plakophilin-2, desmoglein-2, and desmocollin-2) have been identified in up to 70 %
of affected probands. Recent experimental models confirm that this genetically determined
cardiomyopathy develops after birth due to progressive myocardial dystrophy. There
is no single diagnostic "gold standard", and in 2010 a revision of the diagnostic
criteria, encompassing familial, electrocardiographic, arrhythmic, morphofunctional,
and histopathologic findings, was made to improve diagnostic sensitivity, but maintaining
diagnostic specificity. Quantitative parameters for imaging, tissue characterization,
ECG, and signal averaged ECG have been introduced, and the identification of a pathogenic
mutation in a first degree relative has become a major criterion. Genotype–phenotype
correlations, including magnetic resonance and pathology studies on heart specimens
coming from heart transplant or sudden death, are currently demonstrating that the
spectrum of the disease, usually referred to with the adjective "right ventricular",
is wider than initially thought, with the evidence of biventricular or even isolated
left ventricular forms, so that it is increasingly identified simply as "arrhythmogenic
cardiomyopathy". Experimental cellular and animal models are mandatory to try to gain
an insight into the cascade of cellular and molecular events leading from gene defect
to myocardial dystrophy in AC.
A 16 — Disease mechanisms in arrhythmogenic cardiomyopathy: immunohistochemistry and
beyond
Jeffrey E. Saffitz
Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, USA
jsaffitz@bidmc.harvard.edu
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a primary myocardial disorder
characterized by an especially high incidence of ventricular arrhythmias and sudden
death. The identification of desmosomal gene mutations in ∼50 % of patients has led
to the idea that ARVC is a disease of abnormal cell–cell adhesion. However, recent
insights gained largely from studies of the human disease suggest a greater degree
of complexity. These insights include observations that: (1) plakoglobin (γ-catenin)
is consistently redistributed from desmosomes to intracellular/nuclear sites in all
forms of ARVC regardless of the underlying mutation, (2) ARVC patients have elevated
circulating cytokine levels and myocardial production of cytokines, and (3) disease
flares often follow strenuous exercise in ARVC patients. These and other observations
have helped us to propose an overarching working model of the disease pathway in ARVC.
A central feature of this model is that desmosomal mutations in ARVC result in abnormal
responses to mechanical load which, in turn, promote subcellular redistribution of
plakoglobin and induce cytokine expression. Redistribution of plakoglobin from junctional
to intracellular/nuclear pools sets the stage for altered canonical and non-canonical
Wnt signaling pathways with potential changes in gene expression and perturbation
of Ca2+ homeostasis. Cytokines locally expressed by injured cardiac myocytes may promote
development of fibrogenic and adipogenic phenotypes in the myocardium through paracrine
effects on resident fibroblasts and progenitor cells. Altered cellular biomechanics
downstream of ARVC-causing mutations also promote gap junction remodeling and cardiac
myocyte apoptosis. Collectively, these alterations lead to cell injury, promote arrhythmogenesis,
and contribute to the pathology of the disease. We now have multiple lines of evidence
from studies of human disease and experimental systems to support major aspects of
this disease model and to inform future studies. The hope is that insights gained
about mechanisms of cell injury and arrhythmogenesis in ARVC may apply to more common
forms of heart disease and sudden cardiac death.
A 17 — Complex genetic behavior in arrhythmogenic cardiomyopathy and the effect on
disease mechanisms
Jeffrey A. Towbin
The Heart Institute and The Kindervelt–Samuel Kaplan Professor and Chief, Pediatric
Cardiology, Cincinnati Children´s Hospital Medical Center, Cincinnati, OH, USA
jeffrey.towbin@cchmc.org
Objective: to define the genetic and mechanistic basis of arrhythmogenic cardiomyopathy.
Background: arrhythmogenic cardiomyopathy, previously known as arrhythmogenic right
ventricular dysplasia (ARVD) or arrhythmogenic right ventricular cardiomyopathy (ARVC),
is characterized by myocardial fibrofatty replacement, ventricular dysfunction, and
arrhythmias associated with sudden death. Autosomal dominant inheritance is most common,
and reduced penetrance is the rule of thumb, but the underlying basis of low penetrance
is poorly understood. The causative genes identified to date are generally associated
with desmosome function, the "final common pathway" of this disease. We previously
described compound and digenic heterozygosity as a feature of this disorder which
plays a role in the development of the clinical phenotype and the severity of disease.
We have continued to perform genetic screening of 275 probands and families with arrhythmogenic
cardiomyopathy, and have identified mutations in desmosome-encoding genes, as well
as in genes that are not primarily involved in the desmosome but disrupt the desmosome
when mutated in at-risk domains. In addition, we have developed animal models of several
of these genes, and these models are providing insight into the biology of the phenotype.
These genes will be discussed, and the animal models developed will also be described,
along with data on potential mechanisms of disease. Together, the data presented will
support the concepts that: (1) the complex genetic basis of arrhythmogenic cardiomyopathy
includes reduced penetrance with compound and digenic heterozygosity, (2) genes encoding
non-desmosomal proteins result in arrhythmogenic cardiomyopathy by disrupting desmosome
function by abnormal protein–protein interactions, and (3) disturbed junctional cytoarchitecture
in subjects and animals with gene mutations that alter the desmosome confirms that
arrhythmogenic cardiomyopathy is a disease of the desmosome and cell junctions.
[Note: This topic was not orally presented because the invited speaker could not attend
the workshop for health reasons]
A 18 — Naxos cardiocutaneous syndrome: recessive and dominant forms
Adalena Tsatsopoulou, Nikos Protonotarios
Yannis Protonotarios Medical Center, Hora Naxos, 84300, Greece
adalena@otenet.gr
Naxos cardiocutaneous syndrome associates arrhythmogenic cardiomyopathy with hair
and skin abnormalities. The original description of the syndrome has been reported
in 1986 for families originating from the Aegean island of Naxos as a recessively
inherited association of woolly hair, palmoplantar keratoderma and arrhythmogenic
right ventricular cardiomyopathy, given the name of "Naxos disease".
The disease phenotype initially presents with woolly hair from infancy developing
palmoplantar hyperkeratosis along with the increasing use of hands and feet. The cardiomyopathy
becomes clinically apparent during adolescence or young adulthood, with ventricular
arrhythmias, depolarization/repolarization changes in resting ECG, and structural/functional
abnormalities of the right as well as the left ventricle, detected on two-dimensional
echocardiography and cardiac magnetic resonance. Symptomatic presentation is with
syncope, episodes of sustained ventricular tachycardia, or even sudden death. Heart
failure might appear at the end stages of the disease, or earlier in cases with severe
or predominant left ventricular involvement, as in the Carvajal variety of the Naxos
cardiocutaneous syndrome. Cardiac pathology reveals myocyte loss and fibrous or fibrofatty
replacement of myocardium, involving mostly subepicardial and mediomural layers. Up
to now, families showing members with Naxos disease have also been identified on other
Aegean islands. Moreover, cases from India, Ecuador, Italy, Israel, Saudi Arabia,
Turkey, United Kingdom, Spain, and Finland have been reported with increasing frequency.
They mostly appear with autosomal recessive inheritance, but autosomal dominant cases
have also been described.
A 2-base-pair deletion mutation in plakoglobin, a key protein involved in cell–cell
adhesion and signaling, was the first identified gene to cause Naxos cardiocutaneous
syndrome, and indicated an involvement of deficient cell–cell adhesion in the pathogenesis
of arrhythmogenic cardiomyopathy. Subsequently, mutations in the desmosomal plaque
protein desmoplakin (DSP) and recently in the transmembrane glycoprotein desmocollin-2
have been found to be associated with recessive forms of Naxos cardiocutaneous syndrome,
while dominant or digenic DSP mutations have been also related to the syndrome. The
clinical appearance of cardiomyopathy with respect to the predominance of right or
left ventricular involvement seems to be related to the site of cell junction plaque
where the causative mutation is effective, i.e., mutations of desmoplakin truncating
the desmin-binding site of the molecule lead either to predominant left ventricular
involvement or to left dominant arrhythmogenic cardiomyopathy overlapping clinically
with dilated cardiomyopathy (Carvajal syndrome). Dominant forms usually show milder
palmoplantar keratoderma, while woolly hair is a constant finding in either dominant
or recessive cases. The associated skin defects apparent from early infancy on enable
the identification of individuals with concealed heart disease when arrhythmogenic
cardiomyopathy is in an "incubation" stage. Thus, a clinical "electrocardiographic/arrhythmic"
phase can often be documented to precede structural cardiomyopathy changes; molecular
pathology at this stage has also indicated remodeling of gap junctions and electrical
conduction.
A 19 — Inherited arrhythmia syndromes: clinical and genetic management
Michael H. Gollob
Inherited Arrhythmia Clinic, Division of Cardiology and Department of Cellular and
Molecular Medicine, University of Ottawa Heart Institute, Ottawa, Ontario, Canada
mgollob@ottawaheart.ca
Arrhythmogenic right ventricular cardiomyopathy (ARVC), with an estimated prevalence
of ARVC 1 per 5,000, is characterized by fibrofatty replacement of myocardium. It
affects the right ventricle predominantly but may have left ventricular involvement.
ARVC can result in ventricular arrhythmias, SCD, and right or biventricular dysfunction.
Often sporadic, the condition is familial in up to 50 % of index cases. A pathogenetic
theme for ARVC is the presence of mutations in genes encoding desmosomal proteins.
Desmosomes are a primary component of cell-adhesion junctions, ensuring the structural
and functional integrity of cardiomyocytes. Mutations have been identified in genes
encoding for desmosomal proteins plakophilin-2 (PKP2), desmoplakin (DSP), plakoglobin
(JUP), desmocollin (DSC2), and desmoglein (DSG2). A mutation in the gene encoding
a nondesmosomal protein (TMEM43) has been identified as the cause in a large cohort
of related patients in Newfoundland, Canada. The cellular function of the tmem43 protein
is still uncertain. The epidemiological situation of the "Newfoundland cluster" and
the health management consequences are disucssed. In addition, the involvement of
cardiac gap junctions in atrial fibrillations is emphasized.
A 20 — Carvajal/Naxos syndrome secondary to desmoplakin-dominant mutation is associated
with dilated cardiomyopathy, woolly hair, palmoplantar keratoderma and hypo/oligodontia
Lara Chalabreysse1,2,5, Faiza Senni1,5, Patrick Bruyère3, Brigitte Aime1, Christophe
Ollagnier1, André Bozio4, Patrice Bouvagnet
1,4,5
(1) Laboratoire Cardiogénétique, (2) Service de Pathologie, (3) Service de Chirurgie
Maxillo-faciale et Stomatologie, (4) Service Cardiologie Pédiatrique, Hôpitaux de
Lyon, Lyon, France (5) Université de Lyon, F-69008 Lyon, France
patrice.bouvagnet@chu-lyon.fr
There is evidence that Carvajal (woolly hair, palmoplantar keratoderma and dilated
cardiomyopathy) and Naxos (same hair and skin anomalies, with fibrofatty cardiomyocyte
replacement in the right ventricle) syndromes are variable expressions of the same
syndrome secondary to mutations in genes encoding proteins of the desmosome. Here
we report an additional sign that might be helpful to cardiologists in establishing
the diagnosis. The proband had three episodes (at age 15, 16 and 27) of chest pain
with transient ST elevation in leads V3–V4 and mild rise of troponin. He had LV enlargement
(diastolic diameter 64 mm) with normokinetics and no coronary anomalies. He had good
adaptation to physical activity, but numerous premature beats disappearing during
physical stress. He had palmoplantar keratoderma, woolly hair, and was missing the
left mandibular 2nd molar and all 3rd molars. A younger brother had two fainting episodes
when he was 17. He had incomplete RBBB and dilated left ventricle with normokinetics.
Four years later, he had shortness of breath with LV at 70 mm and EF at 20 %. He had
runs of ventricular tachycardia. He received a heart graft. His heart had enlarged
ventricles with fibrofatty replacement in the right ventricle. He had palmoplantar
keratoderma, woolly hair, and marked oligodontia with only four permanent molars and
several persisting primary teeth. The father, who experienced several fainting spells,
had also a dilated cardiomyopathy with the same skin, hair, and teeth anomalies. The
desmoplakin (DSP) and plakoglobin (JUP) genes were screened for mutations, and a single
heterozygous mutation was found in the DSP gene: p.Ser597Leu. This residue is conserved
across vertebrates and absent from 100 controls. The mutation was found in the two
brothers and their father, but absent from all other family members. Conclusion: heterozygous
missense mutation in the DSP gene may result in chest pain, fainting episodes, and
dilated cardiomyopathy. The association of woolly hair, palmoplantar keratoderma,
and/or oligodontia may help in establishing the diagnosis of Carvajal/Naxos disease.
A 21 — Reduction of preload: a pathophysiological approach to therapy in arrhythmogenic
right ventricular cardiomyopathy?
Paulus Kirchhof
Birmingham University, UK, and University Hospital Münster, Germany
KirchhP@ukmuenster.de
The observations and thoughts reported here have been published in JACC (1).
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an important cause of sudden
death in the young (2–6). Despite progress in the prevention of sudden cardiac death
in ARVC patients by antiarrhythmic drugs and implanted defibrillators (7–8), there
is no treatment available that slows or prevents development of ARVC (2, 9–10).
Mutations in genes encoding for mechanical cell–cell contact proteins are found in
ARVC patients (11–17). Transgenic mouse models have verified the biological relevance
of mechanical cell–cell contact dysfunction for ARVC. The disease develops in mice
with heterozygous deletion of plakoglobin (18), heterozygous deletion of desmoplakin
(19), and transgenic expression of desmoglein (20). Recent analyses in myocardial
tissue from ARVC patients suggest that reduced immuno-histological plakoglobin light
intensity may be a sensitive and specific marker for ARVC in patients (5). Hence,
genetic defects in the mechanical cell–cell contacts appear to be the underlying pathophysiological
principle of ARVC. Endurance training, especially when performed at a competitive
level, may accelerate the manifestation of ARVC in susceptible individuals (21–22).
Likewise, endurance training accelerates the development of ARVC in heterozygous plakoglobin-deficient
mice (plako+/-, [18]), suggesting that chronically increased volume load may contribute
to development of ARVC in susceptible patients. We therefore tested whether reducing
ventricular pressure and volume load can prevent or slow training-induced development
of ARVC.
Objective: We used a murine model of arrhythmogenic right ventricular cardiomyopathy
(ARVC) to test whether reducing ventricular load prevents or slows development of
this cardiomyopathy.
Methods: Littermate pairs of heterozygous plakoglobin-deficient mice (plako+/-) and
wild-type (WT) littermates underwent 7 weeks of endurance training (daily swimming).
Mice were randomized to blinded load-reducing therapy (furosemide and nitrates) or
placebo.
Results: Therapy prevented training-induced right ventricular (RV) enlargement in
plako+/- mice (RV volume: untreated plako+/- 136±5μl; treated plako+/- 78 ± 5 μl;
WT 81 ± 5 μl; p < 0.01 for untreated vs WT and untreated vs treated; mean ± SEM).
In isolated, Langendorff-perfused hearts, ventricular tachycardias (VT) were more
often induced in untreated plako+/- hearts (15/25) than in treated plako+/- hearts
(5/19) or in wild-type hearts (6/21, both p < 0.05). VT occurred due to macro-reentry
and decreased RV longitudinal conduction velocity in untreated but not in treated
plako+/- mice (p < 0.01 for untreated vs WT and untreated vs treated). Myocardial
concentration of phosphorylated connexin43 was lower in plako+/- hearts with VTs compared
to hearts without VTs, and was reduced in untreated plako+/- compared to WT (both
p < 0.05). Plako+/- hearts showed reduced myocardial plakoglobin concentration, while
β-catenin and N-cadherin concentration was not changed.
Conclusions: Load-reducing therapy prevents development of ARVC in plako+/- mice,
and may provide a simple approach to preventing disease progression in ARVC patients.
This potential effect of preload reduction should be tested in a controlled clinical
trial.
1. Fabritz L, Hoogendijk M, Scicluna BP, Van Amersfoorth SC, Fortmueller L, Wolf S
et al (2011) Preload-reducing therapy prevents expression of arrhythmogenic right
ventricular cardiomyopathy in plakoglobin-deficient mice. J Am Coll Cardiol 57:740–750
2. Marcus FI, McKenna WJ, Sherrill D, Basso C, Bauce B, Bluemke DA et al (2010) Diagnosis
of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification
of the task force criteria. Circulation 121(13):1533–1541
3. Corrado D, Basso C, Pavei A, Michieli P, Schiavon M, Thiene G (2006) Trends in
sudden cardiovascular death in young competitive athletes after implementation of
a preparticipation screening program. Jama 296(13):1593–1601
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A 22 — Sudden death in athletes
Gaetano Thiene
Department of Medico-Diagnostic Sciences and Special Therapies, University of Padua
Medical School, Padua, Italy
gaetano.thiene@sanita.padova.it
Sudden death in athletes occurs due to hidden cardiac disorders which, often during
effort, may jeopardize heart electrical stability, triggering ventricular fibrillation.
Apart from rare conditions of ion channel diseases in a structurally normal heart,
in which the disorder may be detected simply by basal or stress test 12 lead ECG,
the anomalies at risk of sudden death may affect the aorta (Marfan syndrome), the
coronary arteries (congenital anomalies, premature atherosclerosis), the myocardium
(hypertrophic and arrhythmogenic cardiomyopathies), the valves (bicuspid aortic valve,
mitral valve prolapse) and the conduction system (preexcitation syndromes). These
disorders are for the most part detectable by ECG and/or echo. The employment of these
methods in screening tests before competitions or other athletic meetings can help
to identify masked anomalies and should play a major role in early diagnosis, risk
stratification and prevention of sudden death.
A 23 — Wnt-Ca
2+
as an integrator of differentiation signaling in the heart
Calum A. MacRae
Cardiovascular Division, Brigham & Women´s Hospital, Boston, MA, USA
camacrae@bics.bwh.harvard.edu
Intercellular junctions have been directly implicated in the pathobiology of several
forms of human cardiomyopathy through human genetic studies. The downstream mechanisms
of the junctional perturbations remain obscure, but to date abnormalities of mechanical
and electrochemical signaling have been identified. We have used the zebrafish to
model multiple aspects of junctional biology during normal and pathological cardiogenesis.
In the first instance, we focused on developing techniques to characterize the dynamics
of intercellular coupling during normal cardiac development. High-resolution optical
voltage mapping, Fura-2 calcium imaging and traditional immunohistochemical techniques
were combined to define cardiomyocyte differentiation and cell coupling at multiple
stages from the linear heart tube stage through to 120hpf, when the zebrafish heart
is highly representative of adult human cardiac physiology. The structural and functional
remodeling of junctions is coupled with cytoskeletal and membrane lipid remodeling
which we are also beginning to characterize. We have identified remarkable plasticity
of cardiomyocyte coupling throughout development, with distinctive regional variation
in the complexity and strength of coupling. These data demonstrate that the myocardial
syncytium is not uniform, but rather consists of a complex series of local networks.
Exploration of a series of zebrafish mutants has identified roles for pathways implicated
in synaptogenesis in the formation of specific regional coupling networks.
Interestingly, non-canonical Wnt signals polarize ventricular myocardial structure
and function, but do not perturb the major ventricular cardiomyocyte networks. We
were unable to detect any role for traditional planar cell polarity pathways in the
Wnt-associated polarity changes, but identified a specific role for the L-type calcium
channel in these cellular and physiologic rearrangements. This novel limb of Wnt–calcium
signaling directly connects extracellular and intracellular compartments, and may
serve to integrate canonical and non-canonical Wnt pathways.
Given the role of desmosomal proteins in human cardiomyopathy, we established and
validated multiple zebrafish lines expressing dominant negative mutants implicated
in disease. Using a range of reporter lines, and existing zebrafish Wnt signaling
mutants, there is evidence for both canonical and non-canonical Wnt pathway abnormalities
in desmosomal cardiomyopathies. We have used one of our lines expressing a mutant
plakoglobin line to develop a high-throughput screen for genetic and chemical suppressors
of desmosomal pathology. This line develops a cardiomyopathy with extensive morphologic
and physiologic homology to ARVC, and is associated with reduced survival, sudden
death and congestive heart failure. We are currently evaluating novel Wnt–calcium
pathway members identified in zebrafish, and screening chemical libraries for novel
modulators of desmosomal disease pathways for use as pathway probes, diagnostics or
therapeutic leads.
A 24 — Clinical challenges in ARVC/D: a United States perspective
Hugh M. Calkins
Division of Cardiology, Department of Medicine, Johns Hopkins University School of
Medicine, Baltimore, MD, USA
hcalkins@jhmi.edu
The Johns Hopkins ARVD Program was initiated in 1999 with the goal of furthering research
on ARVD and also providing clinical care for patients with known or suspected ARVD.
During the past 10 years, we have evaluated more than 1,000 patients for this condition.
The purpose of this presentation will be to present our clinical experience with ARVD
and to focus on what we perceive to be the more vital unanswered questions. Particular
emphasis will be placed on describing the remarkable heterogeneity of the clinical
manifestations of the disease. Our aim will be to provide a clinical context for the
remarkable advances in basic research that will be discussed at this meeting.
A 25 — The molecular biology and genetics of blood pressure and its regulation
John J. Mullins
The Centre for Cardiovascular Science, The University of Edinburgh, Queen´s Medical
Research Institute, Edinburgh, UK
j.mullins@ed.ac.uk
Mammalian blood pressure is regulated by a myriad of factors, many of which have been
identified by classical biochemical and physiology experimentation, whilst others
have emerged through genetic studies in both human populations and rodent models.
The advent of genetic manipulation in vivo has facilitated the investigation of mechanisms
underlying inherited forms of hypertension and the cell biology and physiology of
altered blood pressure homeostasis.
Renin is a critical component of a classical renin–angiotensin–aldosterone system
(RAAS), which regulates long-term mammalian blood pressure. We have shown that a threshold
level of expression of the renin is an essential determinant of the morphology and
function of the renal juxtaglomerular cells and of the structure of the anatomically
and functionally related macula densa cells. In genetic rescue experiments, we have
shown that human renin expression in mice lacking endogenous renin1 enzyme rescues
the JG cell deficit but is not sufficient, in isolation, to restore normal macula
densa structure.
Two of the key effectors of the classic RAAS are angiotensin II (Ang II) and aldosterone.
Whilst much attention has been paid to the actions of Ang II in regulating blood pressure,
the dysregulation of the aldosterone axis is also known to lead to profound physiological
and pathophysiological consequences, including a marked elevation of blood pressure.
Aldosterone is not the sole activator of MR in vivo, and glucocoticoids are known
to bind to MR with similar efficiency to that of aldosterone. The relative abundance
of glucocorticoids in the plasma provides the potential for substantive glucocorticoid-mediated
activation of MR. Under normal circumstances, such activation is prevented by the
enzyme 11 beta hydroxysterioid dehydogenase type 2 (11 beta HSDII), which acts locally
to inactivate glucocorticoids and thereby prevents their access to MR, resulting in
the apparent specificity of aldosterone action. Lack of 11 beta HSDII activity in
humans results in the syndrome of apparent mineralocorticoid excess (SAME), a severe
hypertensive disorder with characteristic electrolyte imbalance and a poor prognosis.
We have established a transgenic mouse model of SAME which recapitulates all the key
features of the human condition and facilitates investigation of the underlying mechanism
of the syndrome and the consequences of chronic reduction in the expression of this
critical "gate-keeper" enzyme. Current developments and potential pitfalls of the
use of genetic modification will be discussed, with a focus on its use in investigating
blood pressure homeostasis.
A 26 — The specific molecular ensembles of the junctions connecting mesenchymally-derived
tumor cells, including cardiac myxomata: the coming and going of plakophilin-2
Steffen Rickelt
1,2, Stefania Rizzo3, Mareike Barth1,4, Werner W. Franke1,2
(1) Helmholtz Group for Cell Biology, German Cancer Research Center (DKFZ), Heidelberg,
Germany
(2) Progen Biotechnik, Heidelberg, Germany
(3) Department of Medical-Diagnostic Sciences, University of Padua Medical School,
Padua, Italy
(4) Institute for Pharmacology and Clinical Pharmacology, University Hospital Düsseldorf,
Düsseldorf, Germany
s.rickelt@dkfz-heidelberg.de
In contrast to the advanced state of the molecular characterization of the junctions
connecting epithelial cells, i.e., the intermediate-sized filament (IF)-anchoring
desmosomes (maculae adhaerentes) and the microfilament-associated adherens junctions
(AJs), knowledge of the molecular components of the AJs that connect the diverse types
of mesenchymally-derived cells — normal or malignantly transformed — is still very
limited. Therefore, we have begun to study the molecular composition and the assembly
mechanisms of the AJs connecting the cells of mesenchymally-derived tissues and soft-tissue
tumors. In a systematic study to elucidate the molecular composition of the AJs that
connect non-epithelial cells, we have identified a series of novel and frequent cell
type-specific molecular AJ ensembles, some of which represent unexpectedly new categories
of junctional assemblies, including molecules hitherto only known as major components
of desmosomes in epithelial and carcinomatous cells. Using biochemical and immunocytochemical
as well as electron microscopical methods, we have identified a category of AJs connecting
diverse normal and proliferatively-transformed, mesenchymally-derived cells, which
in addition to N-cadherin and/or cadherin-11 contain a dense cytoplasmic plaque formed
by a- and b-catenin, plakoglobin as well as proteins p120 and p0071, but also major
amounts of the desmosomal plaque proteins plakophilins-2 (Pkp2) and/or -3 (Pkp3).
Such mixed type AJs have been discovered in certain proliferatively active normal
cell culture lines, as well as in malignantly transformed cells (Rickelt et al. 2009).
In particular, we have found this novel AJ type in diverse kinds of human soft-tissue
tumors, including rhabdomyosarcomas, and remarkably consistent in cardiac myxomata
(without exception in all 38 cases examined so far; Rickelt et al. 2010). The specific
correlation of the advent of such Pkp2-positive AJs with the proliferative state of
the given cells is essentially well demonstrable with the interstitial cells of the
cardiac valves (Barth et al. 2009). The possible diagnostic value of Pkp2 in tumor
diagnosis is obvious.
Barth M, Schumacher H, Kuhn C, Akhyari P, Lichtenberg A, Franke WW (2009) Cordial
connections: molecular ensembles and structures of adhering junctions connecting interstitial
cells of cardiac valves in situ and in cell culture. Cell Tissue Res 337:63–77
Rickelt S, Rizzo S, Doerflinger Y, Zentgraf HW, Basso C, Gerosa G, Thiene G, Moll
R, Franke WW (2010) A novel kind of tumor type characteristic junction: plakophilin-2
as a major protein of adherens junctions in cardiac myxomata. Mod Pathol 11:1429–1437
Rickelt S, Winter-Simanowski S, Noffz E, Kuhn C, Franke WW (2009) Upregulation of
plakophilin-2 and its acquisition to adherens junctions identifies a novel molecular
ensemble of cell–cell-attachment characteristic for transformed mesenchymal cells.
Int J Cancer 125:2036–2048
A 27 — N-cadherin antagonists as oncology therapeutics
Orest W. Blaschuk
Division of Urology, Department of Surgery, McGill University, Montreal, Quebec, Canada
N-cadherin is a cell adhesion molecule (for review, see Hulpiau and van Roy 2008)
that plays a pivotal role in promoting blood vessel formation and stability (for review,
see Blaschuk and Devemy 2009). Both of these processes are essential for tumor growth
(for review, see Folkman 2007; Naumov et al. 2008). Initially, I will discuss the
discovery and development of N-cadherin antagonists. These antagonists consist of
three series of compounds: linear peptides (Blaschuk et al. 1990), cyclic peptides
(Williams et al. 2000) and peptidomimetics (Gour et al. 2007). In particular, I will
focus on the effects of these antagonists on endothelial cell adhesion (Erez et al.
2004). Secondly, I will discuss pre-clinical (Shintani et al. 2008; Augustine et al.
2008) and clinical studies (Beasley et al. 2009; Perotti et al. 2009) designed to
ascertain the effects of the N-cadherin antagonist, ADH-1 (a synthetic cyclic pentapeptide)
on tumor growth. Collectively, the data suggest that N-cadherin antagonists might
be useful as anti-cancer agents.
Augustine CK, Yoshimoto Y, Gupt M, Zipfel PA, Selim MA, Febbo P, Pendergast AM, Peters
WP, Tyler DS (2008) Targeting N-cadherin enhances antitumor activity of cytotoxic
therapies in melanoma treatment. Cancer Res 68:3777–3784
Beasley GM, McMahon N, Sanders G, Augustine CK, Selim MA, Peterson B, Norris R, Peters
WP, Ross MI, Tyler DS (2009) A Phase 1 study of systemic ADH-1 in combination with
melphalan via isolated limb infusion in patients with locally advanced in-transit
malignant melanoma. Cancer 115:4766–4774
Blaschuk OW, Devemy E (2009) Cadherins as novel targets for anti-cancer therapy. Eur
J Pharmacol 625:195–198
Blaschuk OW, Sullivan R, David S, Pouliot Y (1990) Identification of a cadherin cell
adhesion recognition sequence. Develop Biol 139:227–229
Erez N, Zamir E, Gour BJ, Blaschuk OW, Geiger B (2004) Induction of apoptosis in cultured
endothelial cells by a cadherin antagonist peptide: involvement of fibroblast growth
factor receptor-mediated signalling. Exp Cell Res 294:366–378
Folkman J (2007) Angiogenesis: an organizing principle for drug discovery? Nat Rev
Drug Discov 6:273–286
Gour BJ, Blaschuk OW, Ali A, Ni F, Chen Z, Michaud SD, Wang S, Hu Z (2007) Peptidomimetic
modulators of cell adhesion. United States Patent Number 7,268,115
Hulpiau P, van Roy F (2008) Molecular evolution of the cadherin superfamily. Int J
Biochem Cell Biol 41:349–369
Naumov GN, Folkman J, Straume O, Akslen LA (2008) Tumor–vascular interactions and
tumor dormancy. APMIS 116:569–585
Perotti A, Sessa C, Mancuso A, Noberasco C, Cresta S, Locatelli A, Carcangiu ML, Passera
K, Braghetti A, Scaramuzza D, Zanaboni F, Fasolo A, Capri G, Miani M, Peters WP, Gianni
L (2009) Clinical and pharmacological phase I evaluation of Exherin (ADH-1), a selective
anti-N-cadherin peptide in patients with N-cadherin-expressing solid tumours. Ann
Oncol 20:741–745
Shintani Y, Fukumoto Y, Chaika N, Grandgenett PM, Hollingsworth MA, Wheelock MJ, Johnson
KR (2008) ADH-1 suppresses N-cadherin-dependent pancreatic cancer progression. Int
J Cancer 122:71–77
Williams E, Williams G, Gour BK, Blaschuk OW, Doherty P (2000) A novel family of cyclic
peptide antagonists suggest that N-Cadherin specificity is determined by amino acids
that flank the HAV motif. J Biol Chem 275:4007–4012
A 28 — The cardiac fibroblast: phenotypes, functions and therapeutic target
Karen E. Porter
Division of Cardiovascular & Neuronal Remodelling, School of Medicine, University
of Leeds, UK
k.e.porter@leeds.ac.uk
Cardiac fibroblasts (CF) are the most prevalent cell type in the mammalian heart,
yet until recent years their role in regulating myocardial function and remodelling
has been largely overlooked in favour of the cardiac muscle cells, cardiomyocytes.
The critical role of CF in maintaining myocardial homeostasis in the healthy heart
is underscored by the need to provide structure, function, and connectivity for all
the myocardial cell types. CF therefore play key roles in regulating not only normal
myocardial function but also during adverse remodelling that occurs with hypertension,
myocardial infarction (MI) and heart failure (HF). Through cell–cell interaction and
secretion of growth factors, cardiomyocyte function is directly modulated by CF and
vice versa. During the myocardial remodelling that follows MI and in HF progression,
CF undergo activation to a myofibroblast phenotype, expressing contractile proteins
such as α-SMA and modulating their function through increased proliferative, migratory,
and secretory properties.
In the remodelling heart, CF are functionally responsive to the elevated levels of
proinflammatory cytokines such as TNF-α and interleukins, vasoactive peptides (e.g.,
angiotensin II, endothelin-1) and hormones (e.g., noradrenaline). Such effects include
changes in cell proliferation, cell migration, extracellular matrix turnover, and
secretion of bioactive molecules including cytokines, peptides, and growth factors.
Although these changes in function are an important adaptive response to myocardial
injury, in the long term they lead to adverse remodelling and heart failure. Many
commonly prescribed cardiovascular therapies (for example ACE inhibitors, beta-blockers,
and statins) also exert pleiotropic effects on cardiac fibroblasts that may explain
some of their benefits in the remodelling heart. In addition, as the importance of
CF emerges and our understanding broadens, modulation of their phenotype and function
may provide a worthwhile goal in the quest for novel, targeted therapeutics.
Mughal RS, Warburton P, O'Regan DJ, Ball SG, Turner NA, Porter KE (2009) Peroxisome
proliferator-activated receptor γ-independent effects of thiazolidinediones on human
cardiac myofibroblast function. Clin Exp Pharmacol Physiol 36:478–486
Porter KE, Turner NA (2009) Cardiac fibroblasts: at the heart of myocardial remodeling.
Pharmacol Ther 123:255–278
Porter KE, Turner NA (2011) Statins and myocardial remodelling: cell and molecular
pathways. Expert Rev Mol Med 13:e22
Porter KE, Turner NA, O'Regan DJ, Balmforth AJ, Ball SG (2004) Simvastatin reduces
human atrial myofibroblast proliferation independently of cholesterol lowering via
inhibition of RhoA. Cardiovasc Res 61:745–755
Turner NA (2011) Therapeutic strategies for targeting the cardiac fibroblast. In:
Turner NA (ed) The cardiac fibroblast. Research Signpost, Kerala, pp 273–285
Turner NA, Porter KE, Smith WH, White HL, Ball SG, Balmforth AJ (2003) Chronic β2-adrenergic
receptor stimulation increases proliferation of human cardiac fibroblasts via an autocrine
mechanism. Cardiovasc Res 57:784–792
A 29 — Cardiac myocyte–fibroblast electrical interactions
Peter Kohl
Chair in Cardiac Biophysics and Systems Biology, National Heart and Lung Institute,
London, UK
p.kohl@imperial.ac.uk
"The heart is a muscle. Muscle is meat. Meat consists of myocytes. If you understand
myocytes, you understand the heart." If this was our conceptual approach to exploring
cardiac structure–function relationships and electro-mechanical activity, we would
be bound to fail. The heart contains more non-myocytes than muscle cells (Vliegen
et al. 1991), and the majority of the former are referred to as fibroblasts (Adler
et al. 1981). The traditional view of fibroblasts is dominated by regarding them as
'obstacles' (from blocking conduction in vivo, to overgrowing cell cultures in vitro).
This perception is shifting, however, to give way to an increasingly integrative appreciation
of the relevance of fibroblasts for proper function of cardiac myocytes (Camelliti
et al. 2005). This trend is evident from increased publication numbers on the topic,
as can be illustrated by a PubMed search for '(fibroblast) AND (heart OR cardiac)':
out of 8,000+ entries returned for the term, more than half have been published in
the past 10 years. As is evident from these numbers, cardiac myocyte–fibroblast interactions
are a huge field. This presentation will focus, therefore, on a small aspect of those
interactions: electrical cross-talk between the heterogeneous cell populations. A
brief introduction of terms and concepts will be followed by a review of insight from
'wet' experimental and 'dry' computational basic research, a consideration of clinical
correlates, an assessment of underlying molecular substrates for electrical cell–cell
interaction, and an outlook that considers current technical and conceptual limitations,
as well as possible solutions—regrettably, however, without answering the 'friend
or foe?' question (Baudino et al. 2006).
Adler CP, Ringlage WP, Böhm N (1981) DNS-Gehalt und Zellzahl in Herz und Leber von
Kindern. Pathol Res Pract 172:25–41
Baudino TA, Carver W, Giles W, Borg TK (2006) Cardiac fibroblasts: friend or foe?
Am J Physiol (Heart Circ Physiol) 291:H1015–H1026
Camelliti P, Borg TK, Kohl P (2005) Structural and functional characterisation of
cardiac fibroblasts. Cardiovasc Res 65:40–51
Vliegen HW, van der Laarse A, Cornelisse CJ, Eulderink F (1991) Myocardial changes
in pressure overload-induced left ventricular hypertrophy: A study on tissue composition,
polyploidization and multinucleation. Eur Heart J 12:488–494
A 30 — Telocytes: a novel kind of mesenchymally derived cells in the heart and in
other organs
Lawrence M. Popescu
1,2
(1) Department of Cellular and Molecular Medicine “Carol Davila”, University of Medicine
and Pharmacy, Bucharest, Romania
(2) Department of Advanced Studies, “Victor Babes” National Institute of Pathology,
Bucharest, Romania
lpopescu@jcmm.org
We have recently described a novel type of interstitial cells — telocytes (TC) — in
several cavitary and non-cavitary organs, from humans and mammals (Popescu and Faussone-Pellegrini
2010). TC were found in all the three concentric layers of heart: epi-, myo- and endocardium
(see www.telocytes.com). Their presence was repeatedly confirmed and, moreover, a
"map" of TC localization in heart was established (Liu et al. 2011). TC have a small
body, but specific (unique) prolongations, that we named telopodes (Tp). Therefore,
the simplest definition of telocytes (TC) is: cells with Tp. Tp are characterized
by: (a) number (1–5, frequently 2–3), (b) length (several tens up to hundreds of micrometers),
(c) moniliform aspect: alternation of dilated segments (podoms) and thin segments
(podomers — less than 200 nm thickness, below the resolving power of light microscopy,
explaining the fact that TC were overlooked so far), (d) podoms accommodating mitochondria,
endoplasmic reticulum (ER) and caveolae — the so-called “Ca2+ uptake/release units”,
and (e) dichotomous branching pattern, making a 3D network, a labyrinthine system
with particular ultrastructural homo- and hetero-cellular junctions. It is worthy
of note that TC and especially Tp release microvesicles (mean diameter of 180 nm),
sending macromolecular signals to neigboring cells and eventually modifying their
transcriptional activity.
The immunophenotype of TC includes mainly CD 34, CD117/c-Kit, and vimentin, but also
caveolin-1, CD44, NOS-2, desmin, cadherin-11, PDGF-R beta and so on. Although for
the time being, electron microscopy remains the election method to precisely identify
TC, double-positive immunostaining with CD34/c-Kit (mainly for cell body) or CD34/vimentin
(mainly for Tp) also represents a useful marker for TC. MicroRNA profile of TC is
characterized by the absence of miRs 1, 133a, 208a, specific for cardiomyocytes, but
the distinct presence of miR 608. Micro RNAs 126-3p, 151-5p, and 193 are differentially
expressed by TC in comparison with other interstitial cells (e.g., fibroblasts), as
resulted from laser capture microdissection. TC contain measurable quantities of angiogenic
microRNAs (e.g., let-7e, 10a, 21, 27b, 100, 130a, 143, 155, 503) (Manole et al. 2011).
It is worthy of mention that TC have a diverse paracrine secretion (VEGF, NO, IL6,
chemokines), as suggested by immunohistochemistry and confirmed by SELDI-TOF mass
spectrometry and xMAP technology (Luminex) for TC in tissue culture. In cell cultures,
when compared to fibroblasts (3T3), TC produced 8 times more IL6 and 3 times more
VEGF respectively. Transmission electron microscopy and electron tomography revealed
complex junctions between TC and cardiomyocytes, as well as nanostructural junctions
between TC and resident progenitor cells, at the level of epicardial stem cell niches
(Gherghiceanu and Popescu 2010, 2011). It is worthy of note that close contacts between
TC and putative progenitor cells were also found at the level of interstitial stem
cell niches in lungs (Popescu et al. 2011), as well as in skeletal muscle (Popescu
et al. 2011). TC, with their Tp, surround cardiac progenitors or precursors to guide
them to form the coherent 3D myocardial architecture. Apparently, Tp provide “tracks”
for the sliding of cardiomyocyte precursors in their development and integration as
working cardiomyocytes.
In conclusion, in the adult mammalian heart, TC together with resident stem cells
and cardiomyocyte progenitor sustain a continuous cardiac renewal process, and might
be key players in repairing the damaged heart. TC “nurse” the progenitor cells in
stem cell niches. The tandem TC–stem cells could be a better option for therapy rather
than stem cells alone. Last but not least, TC are directly (physically) and indirectly
(chemically) involved in neoangiogenesis after myocardial infarction.
Gherghiceanu M, Popescu LM (2010) Cardiomyocyte precursors and telocytes in epicardial
stem cell niche: electron microscope images. J Cell Mol Med 14:871–877
Gherghiceanu M, Popescu LM (2011) Heterocellular communication in the heart: electron
tomography of telocyte–myocyte junctions. J Cell Mol Med 15:1005–1011
Liu JJ, Shen XT, Zheng X, Li Z, Wang J, Q XF (2011) Distribution of telocytes in the
rat heart. J Clin Rehabil Tissue Eng Res 15:3546–3548
Manole CG, Cismasiu V, Gherghiceanu M, Popescu LM (2011) Experimental acute myocardial
infarction: telocytes involvment in neo-angiogenesis. J Cell Mol Med 15:2284–2296
Popescu LM, Faussone-Pellegrini MS (2010) Telocytes – a case of serendipity: the winding
way from interstitial cells of Cajal (ICC), via interstitial Cajal-like cells (ICLC)
to telocytes. J Cell Mol Med 14:729–740
Popescu LM, Gherghiceanu M, Suciu LC, Manole CG, Hinescu ME (2011) Telocytes and putative
stem cells in the lungs: electron microscopy, electron tomography and laser scanning
microscopy. Cell Tissue Res 345:391–403
Popescu LM, Manole E, Serboiu CS, Manole CG, Suciu LC, Gherghiceanu M., Popescu BO
(2011) Identification of telocytes in skeletal muscle interstitium: implication for
muscle regeneration. J Cell Mol Med 15:1379–1392
A 31 — Periostin/filamin A: a candidate central regulatory mechanism for valvular
fibrogenesis and matrix compaction
Roger Markwald, Russell Norris, Suniti Misra, Shibnath Ghatak
Cardiovascular Developmental Biology Center, Department of Regenerative Medicine,
Medical University of South Carolina, Charleston, SC, USA
markwald@musc.edu
Periostin (PN) is a fasciclin-related protein secreted by prevalvular primordial mesenchyme
of the developing ventricular inlets and outlets. It is also expressed by interstitial
cells of the embryonic and adult ventricular myocardium. We have previously shown
that PN promotes cell autonomous, fibrogenic differentiation and the compaction of
a collagenous matrix into mature valve leaflets and cusps. Loss of periostin inhibits
differentiation into fibroblast lineages, collagen secretion and matrix compaction,
resulting in abnormally elongated, myxomatous valves with potential for prolapse and
regurgitation. With respect to mechanism(s), PN, as a matricellular protein, may promote
matrix compaction and maturation by directly binding to collagen (thereby increasing
cross-linking) or indirectly by binding to integrins and potentially initiating signaling
changes in cytoskeleton organization that modify the contractile forces that mediate
matrix compaction. To test the latter mechanism, we initiated signaling studies and
a 3D assay to determine if PN promoted matrix compaction by activating integrin-associated
signaling pathways, and if such activation included phosphorylation of A (FLNA), an
actin binding, cytoskeletal protein specifically expressed in cardiac valve and interstitial
fibroblasts. IP data, Western blots and immunostaining indicated that PN binding to
3 integrin specifically promoted phosphorylation of FLNA (a.a. 2152) by activating
cdc42 and pak1 kinases, and that the 2152 phosphorylation site of FLNA occurred near
two point mutations (P673Q and G228R) found in patients with degenerative (myxomatous)
valve diseases. Silencing or deleting periostin inhibited 2152 FLNA phosphorylation,
which correlated with reduced potential of prevalvular interstitial cells (also ventricular
fibroblasts) to compact collagen gels. Introducing the P673Q and G228R mutations into
mouse prevalvular mesenchyme inhibited both collagen compaction and the phosphorylation
of FLNA (2152). Fibroblasts from patients with P673Q and G228R mutations or mouse
fibroblasts expressing one or more of these mutations or silencing vectors for PN
also exhibited reduced binding of an enzyme — transglutaminase 2 (TG2) — which covalently
links serotonin to FLNA. Pharmacologically or genetically inhibiting "serotonylation"
of FLNA strongly suppressed matrix compaction and valve maturation. Together, these
findings indicate that PN can regulate valvulogenesis and matrix maturation by triggering
integrin-dependent signaling mechanisms that target FLNA and its potential to generate
cytoskeletal contractile forces through an interaction with TG2 and serotonin.
[Supported by NHLBI, AHA, NCRR and Leducq Mitral Transatlantic Network.]
A 32 — Molecular mechanisms of heart valve development and disease
Elaine E. Wirrig, Jonathan D. Cheek, Santanu Chakraborty, Christina M. Alfieri, Robert
B. Hinton,
Katherine E. Yutzey
The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH,
USA
katherine.yutzey@cchmc.org
Studies of human explanted aortic valves and mouse models were used to define molecular,
cellular, and morphogenetic features of heart valve disease progression. In human
diseased aortic valves, valvular interstitial cell (VIC) activation, extracellular
matrix (ECM) disorganization, and induction of markers of valve mesenchymal and cartilage
progenitor cells are observed in both pediatric and adult diseased aortic valves.
In contrast to calcific valve disease in adults, pediatric diseased aortic valves
do not calcify, and expression of osteogenic markers is apparent in adult, but not
pediatric, diseased aortic valves. Interestingly, phospho-Smad1/5/8 also is increased
in adult calcified valves, suggesting that BMP signaling contributes to heart valve
calcification. Osteogenesis imperfecta murine (Oim) mice have a mutation in Col1a2
that affects collagen fibrillogenesis and leads to bone fragility. The valves of Oim/Oim
mice have decreased collagen and increased proteoglycan composition with leaflet thickening.
In addition, the Oim/Oim mice have increased expression of valve and cartilage progenitor
markers, consistent with increased proteoglycan composition and absence of calcification.
Klotho-null mice are a model for premature aging, and exhibit calcified nodules in
aortic valves in the absence of leaflet thickening or ECM disorganization. Klotho-null
aortic valves have increased expression of the transcription factor Runx2, consistent
with the calcified phenotype, in addition to increased expression of cartilage marker
genes. Together, these findings demonstrate specific molecular indicators of aortic
valve disease progression, which could lead to identification of early disease markers
and the development of therapeutic interventions.
A 33 — Next generation sequencing in ARVC mutation detection and new genes for desmosomal-like
disease
David P. Kelsell
The Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen
Mary University of London, London, E1 4AT, UK
d.p.kelsell@qmul.ac.uk
The importance of desmosomes for maintenance of the strength and flexibility of these
tissues is highlighted by natural and in vitro engineered mutations in desmosomal
genes, which compromise skin or heart and in some instances both. Indeed, desmosomal
gene mutations account for 45–50 % of cases of arrhythmogenic right ventricular cardiomyopathy
(ARVC). ARVC is a disease of ventricular myocardium, which on macroscopic histological
examination reveals ventricular dilatation, thinning of affected myocardium, and areas
of scarring. Detailed genetic sequencing has now identified both heterozygous and
mutations in all five major proteins within the desmosome. The current detection rate
of pathogenic mutations in non-syndromic ARVC is 45–50 %, with mutations most commonly
seen in PKP-2 and least frequently seen in PG. In this presentation, the role of targeted
capture followed by next-generation sequencing in ARVC mutation identification will
be described. In an initial study of 12 patients clinically diagnosed with ARVC but
not yet genotypically characterised, nine desmosome protein mutations were identified,
of which seven were novel.
In addition, we have used next-generation sequencing to discover new genes linked
with the regulation of desmosome function. For example, we studied two siblings with
autosomal recessive neonatal inflammatory skin and bowel lesions. The affected female
died suddenly aged 12 of parvovirus B19 myocarditis, and her brother has mild cardiomyopathy.
We have identified the first human loss-of-function mutation in ADAM17 [encoding a
disintegrin and metalloproteinase 17, ADAM17, also called 'tumor necrosis factor (TACE)'-converting
enzyme)] as the likely underlying cause of this syndrome (Blaydon, Biancheri et al.
2011). Functional studies revealed defective DSG2 processing. We have also recently
identified loss-of-function mutations in the gene for protease inhibitor cystatin
A (CSTA) as the underlying genetic cause of exfoliative ichthyosis (Blaydon, Nitoiu
et al. 2011).
Electron microscopy of patient skin biopsies revealed that the level of skin peeling
occurs between the basal and suprabasal layers in these patients. In addition, in
vitro modelling suggests that in the absence of cystatin A protein, there is a cell–cell
adhesion defect in human keratinocytes that is particularly prominent when cells are
subject to mechanical stress. This is the first evidence of a key role for a protease
inhibitor in epidermal adhesion within the lower layers of the human epidermis. Further
functional studies describing the effect of ADAM17 and CSTA gene mutations in keratinocytes
and desmosome biology will be described.
[The two papers below were in press at the time of Heidelberg Heart II.]
Blaydon DC, Biancheri P, Di WL, Plagnol V et al (2011) Inflammatory skin and bowel
disease linked to ADAM17 deletion.N Engl J Med 365:1502–1508
Blaydon DC, Nitoiu D, Eckl KM, Cabral RM et al (2011) Mutations in CSTA, encoding
Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor
in cell–cell adhesion. Am J Hum Genet 89(4):564–571
A 34 — The living aortic valve: functional and clinical relevance
Sir Magdi H. Yacoub
Imperial College London, National Heart & Lung Institute, Harefield Heart Science
Centre, Harefield, Middlesex UB9 6JH, UK
m.yacoub@imperial.ac.uk
Until recently, heart valves were thought of as passive structures, which are driven
by haemodynamic events, with the sole function of guaranteeing unidirectional flow
with minimal or no obstruction. Recent evidence has shown that heart valves perform
extremely sophisticated functions which depend on their viability and the specific
characteristics of their component parts, at tissue, cellular, and molecular levels.
This enables the valves to alter their shape, size and mechanical properties during
different phases of the cardiac cycle, and to respond to the continuously changing
haemodynamic conditions during health and disease. Such changes have been shown to
influence myocardial function, coronary flow, and other organ functions.
Currently, the only valve substitute which guarantees long-term viability of the inserted
graft is the pulmonary autograft or the Ross operation. A recent prospective randomised
trial comparing the results of the Ross operation to non-viable aortic homograft roots
showed significantly better survival and quality of life following the Ross operation,
which is thought to be largely due to the viability of the pulmonary autograft. Taken
together, these findings support the concept of tissue engineering viable tissue valves.
A 35 — Heart valves — concepts for tissue engineering
Serghei Cebotari1, Igor Tudorache1, Anatol Ciubotaru2, Dietmar Boethig1, Samir Sarikouch1,
Adelheid Goerler1, Artur Lichtenberg1, Eduard Cheptanaru2, Sergiu Barnaciuc2, Anatol
Cazacu2, Oxana Maliga2, Oleg Repin2, Liviu Maniuc2, Thomas Breymann1, Axel Haverich
1
(1) Department of Thoracic and Cardiovascular Surgery, Hannover Medical School, Germany
(2) Cardiac Surgery Center, State Medical and Pharmaceutical University, Chisinau,
Moldova
haverich.axel@mh-hannover.de
Degeneration of xenografts or homografts is a major cause for reoperation in young
patients after pulmonary valve replacement. Here we present the early results of fresh
decellularized pulmonary homografts (DPH) implantation compared to glutaraldehyde-fixed
bovine jugular vein (BJV) and cryopreserved homografts (CH). Thirty-eight patients
with DPH in pulmonary position were consecutively evaluated during the follow-up (up
to 5 years), including medical examination, echocardiography, and MRI. These patients
were matched according to age and pathology and compared to BJV (n = 38) and CH (n =
38) recipients. In contrast to BJV and CH groups, echocardiography revealed no increase
of transvalvular gradient, cusp thickening, or aneurysmatic dilatation in DPH patients.
Over time, DPH valve annulus diameters converge towards normal z-values. Five-year-freedom
from explantation was 100% for DPH; 86 ± 8 % and 88 ± 7 % for BJV and CH conduits
respectively. Additionally, MRI investigations in 17 DPH patients with follow-up time
>2 years were compared to MRI data of 20 BJV recipients. Both patientís groups (DPH
and BJV) were at comparable ages (mean 12.7 ± 6.1 versus 13.0 ± 3.0 years old) and
have comparable follow-up time (3.7 ± 1.0 versus 2.7 ± 0.9 years). In DPH patients,
the mean transvalvular gradient was significantly (p = 0.001) lower (11 mmHg) than
in the BJV group (23.2mmHg). Regurgitation fraction was 14 ± 3 % and 4 ± 5 % in the
DPH and BJV groups respectively. In three DPH recipients, moderate regurgitation was
documented postoperatively, and remained unchanged in follow-up. Conclusions: in contrast
to conventional homografts and xenografts, decellularized fresh allograft valves showed
improved freedom from explantation, provided low gradients in follow-up and exhibited
adaptive growth. This concept may be transferred to myocardial tissue engineering,
where most interesting results have been obtained already.
A 36 — Relevance of understanding valve interstitial and endothelial cell biology
to tissue engineering heart valves
Adrian H. Chester
Imperial College London, National Heart & Lung Institute, Harefield Heart Science
Centre, Harefield, Middlesex UB9 6JH, UK
a.chester@imperial.ac.uk
The cellular components of heart valves play a key role in the function and durability
of these highly dynamic and complex structures. Heart valve interstitial and endothelial
cells both possess unique phenotypic characteristics and functional responses, which
allow then to maintain the integrity of valve structure in conditions of a rapidly
changing mechanical environment. We, and others, have studied how valve cells respond
to growth factors and mechanical cues, to promote cell proliferation and extracellular
matrix secretion; optimise the dispensability of valve tissue and retard the development
of calcific lesions. These properties rely on communication between the cells and
the extracellular matrix, as well as paracrine signalling between endothelial and
interstitial cells. These events regulate the secretory and contractile capacity of
the interstitial cells.
Understanding the biology of valve cells and the valve extracellular matrix is only
the first step in an attempt to tissue engineering a heart valve. Comparative assessment
of the responses of candidate cells will provide a rationale for using a particular
cell type to tissue engineer a valve. Important characteristics are the development
of a valve cell phenotype, stability of that phenotype, secretory properties, immunogenicity,
and an ability to respond the hemodynamic conditions experienced by valves to promote
a stable and durable structure. In this regard, we have examined the phenotypic and
functional characteristics of mesenchymal stem cells isolated from the bone marrow
and adipose tissue. Our data suggest that these cell types share some properties with
valve interstitial cells, and may also be suitable for differentiation into a valve
endothelial cell phenotype. Understanding the properties of valve endothelial and
interstitial cells that allow them to maintain a healthy valve is required if the
function of these cells is to be recapitulated in tissue engineered valves.
A 37 — Naturally inspired engineering of heart valves: developmental biology meets
regenerative medicine
Jonathan T. Butcher
Department for Biomedical Engineering, Cornell University, Ithaca, NY, USA
jtb47@cornell.edu
Heart valve disease is a serious and growing clinical problem for which the only therapy
is prosthetic valve replacement. These nonliving valves are well-suited for the elderly,
but for younger patients are poorly tolerated. Particularly in children, there is
a significant need for a living valve replacement that can grow and remodel over time.
Our lab has focused on understanding the mechanisms by which these valves are "naturally
engineered" during embryonic development, in order to identify paradigms that can
accelerate the maturation of tissue-engineered replacements. Two ways we do this is
by: 1) using signaling programs grounded in natural developmental valve maturation
to coax stem cells naturally towards heart valve phenotypes, and 2) identifying and
replicating the evolving developmental hemodynamic signals in tissue-engineered conduits.
We employ 3D tissue printing as a means for creating anatomically accurate heterogeneous
structures for valve replacement. We are also using this same engineering approach
to learn more about the hemodynamic causes of congenital heart defects. We have developed
a new method for non-invasive microsurgery of embryonic hearts via focused laser photoablation.
We show that this technique is capable of creating models of congenital heart defects
without genetic mutation. Engineering approaches offer powerful new ways of thinking
about developmental biology that can pay significant dividends towards regenerative
medicine strategies.
A 38 — Endothelial plasticity in cardiac valves
Joyce Bischoff
Children´s Hospital Boston and Harvard Medical School, Boston, MA, USA
joyce.bischoff@childrens.harvard.edu
The endothelium covering the aortic, pulmonary, mitral, and tricuspid valves looks
much like the endothelium throughout the vasculature, in terms of general morphology
and expression of many endothelial markers. Closer examination, however, reveals important
differences and hints of a unique phenotype that reflects the valvular endothelium´s
embryonic history and potentially its ability to maintain integrity and function over
a lifespan of dynamic mechanical stress. A well-studied property that sets the cardiac
valvular endothelium apart is the ability to transition from an endothelial to a mesenchymal
phenotype — an event known as EMT. EMT is a critical step during embryonic valvulogenesis;
it can occur in post-natal valves (Paranya et al. 2001; Paruchuri et al. 2006), and
has recently been implicated in the adaptive response of mitral valve leaflets exposed
to a controlled in vivo setting designed to mimic the leaflet tethering that occurs
in ischemic mitral regurgitation (Dal-Bianco et al. 2009). This presentation will
discuss what is known about valvular endothelial cells, with a particular focus on
EMT in post-natal, adult valves. New data on the plasticity of valvular endothelial
cells will be presented (Wylie-Sears et al. 2011). The self-renewal and multi-lineage
differentiation potential of valvular ECs suggests that at subset of valvular endothelial
cells are progenitor cells, which may serve to replenish valvular cells during normal
cellular turnover and in response to injury and disease.
Dal-Bianco JP, Aikawa E, Bischoff J, Guerrero JL, Handschumacher MD, Sullivan S, Johnson
B, Titus JS, Iwamoto Y, Wylie-Sears J, Levine RA, Carpentier A (2009) Active adaptation
of the tethered mitral valve: Insights into a compensatory mechanism for functional
mitral regurgitation. Circulation 120:334–342
Paranya G, Vineberg S, Dvorin E, Kaushal S, Roth SJ, Rabkin E, Schoen FJ, Bischoff
J (2001) Aortic valve endothelial cells undergo transforming growth factor-beta-mediated
and non-transforming growth factor-beta-mediated transdifferentiation in vitro. Am
J Pathol 159:1335–1343
Paruchuri S, Yang JH, Aikawa E, Melero-Martin JM, Khan ZA, Loukogeorgakis S, Schoen
FJ, Bischoff J (2006) Human pulmonary valve progenitor cells exhibit endothelial/mesenchymal
plasticity in response to vascular endothelial growth factor-a and transforming growth
factor-beta2. Circ Res 99:861–869
Wylie-Sears J, Aikawa E, Levine RA, Yang JH, Bischoff J (2011) Mitral valve endothelial
cells with osteogenic differentiation potential. Arterioscler Thromb Vasc Biol 31:598–607
THE SPECIAL PATIENT CASE
A 39 — Dualism in cardiac pathogenesis: illicit use of anabolic–androgenic steroids
in a shot-put athlete homozygous for a missense desmoglein-2 (Dsg2) mutation
Werner W. Franke (Presentation and Discussion Leader)
Helmholtz Group for Cell Biology, German Cancer Research Center DKFZ, Im Neuenheimer
Feld 280, D-69120 Heidelberg, Germany
w.franke@dkfz.de
In view of the recently increased recognition of the frequency of ARVC/D patients
carrying mutations in constitutive molecular components of the cytoskeleton and the
specific junctions (composite junctions, areae compositae) of the cardiomyocyte-connecting
intercalated disk (see, e.g., van Tintelen, A14, as well as Rickelt and Pieperhoff,
special article, in this issue), it is now necessary to consider the very high ratio
of young persons who take anabolic–androgenic steroids (AAS) for the promotion of
muscle growth and for athletic performance enhancements, including athletes as well
as "bodybuilders" and persons in show business.
Although cross-striated skeletal muscle is the desired target tissue of this drug
abuse, it was not surprising to learn that cross-striated myocardiac muscle can also
increase in size and protein mass (for early animal experiments and reviews, see 'Special
Reference List'). This possible coincidence of a genetic predisposition and widespread
drug abuse is therefore a special subject of concern, notably in connection with discussions
of cases of "sudden death" of active or former AAS abusers. As this drug abuse usually
occurs in deeply conspirative secrecy and the persons involved, including family members,
coaches, dealers, and sports functionaries, will remain silent, it would need a rare
and special combination of circumstances to collect and publish the information needed
to present a specific case. Therefore, we thank Mr. Gerd L. Jacobs, born April 4,
1960, in Berlin, for permission to present his case at this meeting.
A slightly condensed summary of his life history is presented in the protocol of his
interrogation by the police in the city of Berlin for the County Court Prosecutors
on February 2 1998 (an English summary of the protocol can be read on the author's
website at http://www.dkfz.de/en/helmholtz-zellbiologie/starting-page-Helmholtz.html).
Mr. Jacobs was an active athlete (track and field) in shot-put and discus throw in
the Berlin sports club TSC from 1972 to 1984, and finished his sports career as a
sports teacher (in the last years of his career he was among the top-ten of the German
Democratic Republic, GDR). His closest club team-mates in shot-put included Ulf Timmermann,
Olympic gold medal winner, former world record holder and still European record holder.
Mr. Jacobs received the oral drug Oral-Turinabol (OT), a 17-α-alkylated steroid, the
most frequently used AAS in GDR sports (Franke and Berendonk 1997). He received the
pills directly from the coach and was never informed about possible AAS-induced damages
or harmful side-effects. The daily dose varied between two and eight pills, i.e.,
10–40 mg. In later years, the dosage was reduced to half. The drug was given in two
annual "cycles", each for 4 months.
After 1998 the cardiac health of Mr. Jacobs deteriorated dramatically and rapidly,
so that on October 1 2004 his heart had to be replaced by a donor heart. The major
statement in the histological diagnosis was "high-grade cardiac muscle hypertrophy
with secondary myocardiac damages and myocardial disarrangements".
Independently, and not aware of the AAS drug history, Posch et al. (2008) had found
that the explanted heart as well as other tissues of Mr. Jacobs contained two missense
mutations in the gene encoding desmoglein-2 (V55M and V919G), i.e., one of the two
cadherin-type transmembrane glycoproteins of the desmosomal type (Schäfer et al. 1994,
1996), the importance of which for the development and functions in non-epithelial
tissues was first demonstrated by Eshkind et al. (2002). Mr. Jacobs has been reported
as homozygous for DSG-V55M, and his father has subsequently been found to be heterozygous
for this mutation but also suffering from "dilated cardiomyopathy". Ultrastructural
alterations have been reported for the intercalated disk junctions of the explanted
heart, including electron microscopy (Posch et al. 2008).
As similar heart problems, including hypertrophic and dilated cardiomyopathies, have
also been found in AAS-treated power athletes and bodybuilders (see 'Special Reference
List'), the combinations of both situations, i.e. gene mutations in one of the constitutive
molecules of the composite junctions (areae compositae) of the myocardial intercalated
disks (for Dsg2 see, for example, Borrmann et al. 2006; Franke et al. 2006; for further
recent reports on Dsg2 mutations in cardiac diseases, see the reference thesaurus
in the article by Pieperhoff and Rickelt in this issue) and AAS-treatment (one of
the most spectacular cases in Berlin was that of the former shot-put European vice
champion Ralf Reichenbach, 48 years old), have to be considered and discussed as a
special possible cause for the specific pathogenic developments.
Eshkind L, Tian Q, Schmidt A, Franke WW, Windoffer R, Leube RE (2002) Loss of desmoglein
2 suggests essential functions for early embryonic development and proliferation of
embryonal stem cells. Eur J Cell Biol 81:592–598
Franke WW, Berendonk B (1997) Hormonal doping and androgenization of athletes: a secret
program of the German Democratic Republic government. Clin Chem 43:1262–1279
Posch MG, Posch MJ, Geier C, Erdmann B, Mueller W, Richter A, Ruppert V, Pankuweit
S, Maisch B, Perrot A, Buttgereit J, Dietz R, Haverkamp W, Özcelik C (2008) A missense
variant in desmoglein-2 predisposes to dilated cardiomyopathy. Mol Genet Metab 95:74–80
Schäfer S, Koch PJ, Franke WW (1994) Identification of the ubiquitous human desmoglein,
Dsg2, and the expression catalogue of the desmoglein subfamily of desmosomal cadherins.
Exp Cell Res 211:391–399
Schäfer S, Stumpp S, Franke WW (1996) Immunological identification and characterization
of the desmosomal cadherin Dsg2 in coupled and uncoupled epithelial cells and in human
tissues. Differentiation 60:99–108
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in German]
Immunofluorescence microscopy of plakophilin-2 (# 651167) and protein myozap (# 651169)
in mammalian heart tissue: Specific decoration of the composite junctions in the intercalated
disks.
# 61075 anti-Cardiac a-Actin, mouse mc
# 61001 anti-a-smooth muscle Actin, mouse mc
# 16109 anti-CD34, mouse mc
# 16105 anti-CD117, mouse mc
# 10519 anti-Desmin, mouse mc
# 10570 anti-Desmin, rabbit pc
# 610120 anti-Desmocollin 2, rabbit pc
# 61059 anti-Desmoglein 2, mouse mc
# 651118 anti-Desmoglein 2, mouse mc
# 651119 anti-Desmoglein 2, mouse mc
# 610121 anti-Desmoglein 2, rabbit pc
# DP-1 anti-Desmoplakin 1, guinea pig pc
# 61024 anti-Desmoplakin 1, mouse mc
# 61003 anti-Desmoplakin 1/2, mouse mc
# 65146 anti-Desmoplakin, mouse mcs
# 651155 anti-Desmoplakin 1/2, mouse mc
# 651109 anti-Desmoplakin 1/2, mouse mc
# 651138 anti-Lamin A/C, mouse mc
# 651169 anti-MyoZap, mouse mc
# GP31 anti-MLDP/OXPAT, C-terminus, guinea pig pc
# GP44 anti-MLDP/OXPAT, N-terminus, guinea pig pc
# 61005 anti-Plakoglobin, mouse mc
# 651101 anti-Plakophilin 2, mouse mc
# 651167 anti-Plakophilin 2, mouse mc
# GP-PP2 anti-Plakophilin 2, guinea pig pc
# 61013 anti-Vimentin, mouse mc
# GP53 anti-Vimentin, guinea pig pc
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Abstracts of poster presentations
P 1 — Study of the molecular pathogenesis of arrhythmogenic cardiomyopathy due to
Desmoglein-2 mutations: the zebrafish helps the mouse
Giorgia Beffagna1, Alessandra Lorenzon1, Martina Milanetto1,2, Roberto Doliana3, Giuseppe
Lembo4, Patrizia Sabatelli5, Daniela Carnevale4, Paolo Grumati2, Emanuela Dazzo1,
Enrico Moro1, Francesco Argenton1, Paolo Bonaldo2, Paola Braghetta2, Alessandra Rampazzo1
(1) Department of Biology, University of Padova, Padova, Italy
(2) Department of Histology, Microbiology, and Medical Biotechnology, University of
Padova, Padova, Italy
(3) Department of Molecular Oncology and Translational Research, CRO-IRCCS, Aviano,
Pordenone, Italy
(4) Department of Angio-Cardio-Neurology, Neuromed Institute Pozzilli, Italy
(5) Unit of Bologna c/o IOR, Division of Experimental Oncology, Bologna, Italy
alessandra.rampazzo@unipd.it
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a progressively degenerative
cardiomyopathy, frequently involved in juvenile sudden death. ARVC is considered a
disease of cell adhesion, because mutations in desmosomal genes have been involved
in the pathogenesis of ARVC in a significant proportion of patients. To identify the
molecular pathogenic mechanisms involved in ARVC, we have generated cardiac-restricted
desmoglein-2 (DSG2) transgenic mice. All the transgenic lines expressing human mutated
DSG2 (G100R, N266S, Q558X) resemble the clinical features of ARVC. At the molecular
level, we checked the expression and localization of some adhesion proteins, demonstrating
changes in expression and localization of beta-catenin in hearts of transgenic mice
carrying the mutated proteins. To establish whether the observed increase in beta-catenin
expression has a possible direct effect on Wnt signaling, we co-injected in zebrafish
embryos the WT and mutated DSG2 mRNAs with BAT-lux reporter plasmids containing the
luciferase enzyme cDNA under the control of the responsive elements of Wnt/beta-catenin
signaling. Luciferase reporter activity occurred significantly higher in fishes injected
with mutant constructs than in those injected with wild type.
To further examine the relationship of beta-catenin and Wnt signaling, we co-injected
dickkopf-1 (Dkk1), an inhibitor of Wnt signalling, and we showed that Dkk1 rescued
the phenotype in embryos. In conclusion, mutations in desmosomal proteins can perturb
the normal balance of critical proteins in junctions and the citosol which, in turn,
could alter gene expression by circumventing normal Wnt signaling pathway.
P 2 — Conduction slowing and arrhythmogenesis in desmoglein-2 mutant mice due to intercalated
disk abnormalities, prior to the development of cardiomyopathic changes
Stefania Rizzo1, Elisabeth M Lodder2, Carol Ann Remme2, Rianne Wolswinkel2, Kalliopi
Pilichou1, Cristina Basso1, Gaetano Thiene1, Connie R Bezzina2
(1) University of Padua, Padua, Italy
(2) University of Amsterdam, Amsterdam, The Netherlands
stefania.rizzo@studenti.unipd.it; e.m.lodder@amc.uva.nl
We investigated whether intercalated disk (ID) remodelling in arrhythmogenic cardiomyopathy
due to desmosomal mutations impacts on cardiac elecrophysiological properties before
the onset of structural changes. We studied transgenic mice with low cardiac overexpression
of N271S-dsg2 (TgNS/L, the mouse homolog of the human mutation DSG2-N266S) at three
different ages: <2 wks, 3–4 wks and >6wks. Mice with cardiac overexpression of wild-type
dsg2 (TgWT) and wild-type served as controls. ECG and epicardial mapping were performed
to determine ventricular conduction and arrhythmia susceptibility. The structure and
molecular composition of the ID was assessed by electron microscopy (EM) and by immunofluorescence.
Cardiomyopathic changes were observed by EM in Tg-NS/L only from >6 wks. At ECG, QRS-prolongation
and spontaneous arrhythmias were observed in TgNS/L only from age >6 wks. However,
on epicardial mapping, ventricular activation time was prolonged in TgNS/L at 3–4
wks (mean ± SEM 11.9 ± 1.8 ms, n = 5) compared to WT (7.6 ± 0.6, n = 4) and TgWT (7.4 ± 0.5,
n = 5) (p < 0.05). In addition in this same age group, ventricular arrhythmias were
inducible in TgNS/L, but not in controls. EM uncovered gap-widening at desmosomes
/adherens junctions, but not in the gap junctions, starting at 3–4 wks exclusively
in TgNS/L mice. No differences in the level and localization of junctional proteins
were found between TgNS/L and controls. Dsg-2 mutant mice display conduction slowing
and ventricular arrhythmias before development of cardiomyopathic changes. This coincided
with the time-point at which junctional gap-widening was observed, suggesting that
ID integrity is required for proper electrical conduction.
P 3 — Development and evaluation of a perfusion decellularization porcine heart model:
generation of three-dimensional myocardial neoscaffolds
Alexander Weymann1, Bastian Schmack1, Carsten Schies1, Nicole Chaimow1, Ines Pätzold1,
Benjamin Claus2, Kristóf Hirschberg1,3, Pál Soós1,3, Sivakkanan Loganathan1, Enikö
Barnucz1, Sevil Korkmaz,1 Pascal Dohmen4, Gábor Szabó1, Matthias Karck1
(1) Department of Cardiac Surgery, Heart Center, University of Heidelberg, Heidelberg,
Germany
(2) Department of Cardiovascular Surgery, Charité–University Medicine Berlin, Campus
Charité Mitte, Berlin, Germany
(3) Heart Center Semmelweis University, Semmelweis University, Budapest, Hungary
(4) Department of Cardiac Surgery, Heart Center, University of Leipzig, Leipzig, Germany
Alexander.Weymann@med.uni-heidelberg.de; Matthias.Karck@med.uni-heidelberg.de
Reports about the generation of three-dimensional neoscaffolds for myocardial tissue
engineering are limited. The architecture provided by perfusion decellularization
of whole human-sized hearts would support the production of three-dimensional living
tissues from an acellular matrix. The aim of this study was to evaluate the potential
of a perfusion decellularization model for whole-heart tissue engineering.
Hearts were obtained from 12 German Landrace pigs from a selected abattoir. After
preparation, the hearts were mounted and perfused on a modified Langendorff decellularization
model specifically constructed for this reason. Decellularization was achieved by
an ionic detergent-based perfusion protocol. The quality of the decellularization
process was quantified by histology and fluorescence microscopy. Data concerning the
presence of residual DNA within the decellularized hearts were measured with spectrophotometric
quantification and compared to controls. For the measurement of mechanical stability,
a micromanometer was advanced into the ventricle and determined LV pressure at different
LV volumes.
The here-described protocol preserved the micro- and macroarchitecture of the hearts.
After histological examination, all hearts lacked intracellular components but retained
various types of collagen, proteoglycan, and elastin. Quantitative DNA analysis demonstrated
a significant reduction of DNA in decellularized hearts compared to controls (84.32
± 3.99ng DNA/mg tissue vs 470.13 ± 18.77ng DNA/mg tissue (p < 0.05)). Using the decellularization
protocol described in the present study, decellularized hearts showed similar mechanical
stability as native hearts. The modified Langendorff perfusion decellularization model
described here is applicable for whole porcine hearts by removing cellular content
and DNA. The resulting three-dimensional matrix provides an interesting tool for further
studies in the field of whole heart tissue engineering.
P 4 — Tissue engineering of the stented pericardium using magnetic guidance for recellularization
Ali Ghodsizad1, Viktor Bordel1, Jose Berjon Gonzalez2, Matthias Karck1, Arjang Ruhparwar1
(1) Department of Cardiac Surgery, University of Heidelberg, Germany
(2) Department of Pathology, The Methodist Hospital, Houston, TX, USA
Matthias.Karck@med.uni-heidelberg.de
Application of progenitor cells for differentiation in a three-dimensional pattern
is an important aspect in tissue engineering. We report on development of a bioreactor
for three-dimensional cell culture experiments using magnetically guided cell recellularization
under simulated physiologic conditions.
Stented pericardial aortic valves were constructed and decellularized by detergents.
Isolated, magnetically labelled human cord-blood-derived unrestricted somatic stem
cells (USSCs) were cultured in the bioreactor for up to 130 hours (n = 8). A magnetic
field was created around the valve within the bioreactor for specific delivery of
circulating cells to their desired targets. In the control group, the magnetic field
was absent. The bioreactor enabled the retention of physiologic culture conditions
with high pulsatile flows , aerobic cell metabolism oxygen tension (pO2 — 130 ± 20
mmHg) and physiological pH values (7.4 ± 0.05) during the whole experimental procedure.
The histological characterization of the matrix and cells was assessed by immunohistochemical
staining and electronic microscopy. Macroscopic and histological analysis showed a
homogeneous seeding of the valve with USSCs in the magnet group, but no seeding of
cells could be observed in the non-magnetic group.
Our modified multifunctional bioreactor allows for three-dimensional culturing of
human cord-blood-derived unrestricted somatic stem cells on pericardial stented valves
with the support of magnetic cell guidance.
P 5 — Osteopontin and CD44 synthesis are increased in fibrotic hearts of desmoglein
2 mutant mice
Phillip Krull, Sebastian Kant, Rudolf E. Leube, Claudia A. Krusche
Institute of Molecular and Cellular Anatomy, Medical Faculty, RWTH Aachen University,
Aachen, Germany
ckrusche@ukaachen.de; rleube@ukaachen.de
Desmoglein 2 (DSG2) mutant mice develop dilative cardiomyopathy characterized by cardiomyocyte
necrosis, calcification, and fibrosis (Krusche, Holthöfer et al., 2011). Since osteopontin
(OPN) is involved in calcification, inflammation, and cardiac fibrosis (Renault et
al. 2010; Matsui et al. 2004; Okamoto et al. 2011), we studied expression and tissue
distribution of OPN and its receptor, the CD44 antigen, which is involved in leukocyte
recruitment (Weber et al. 1996; DeGrendele et al. 1996). mRNA synthesis was assessed
by real-time RT-PCR, and proteins were localized by immunohistochemistry. Wild-type
and homozygous DSG2 mutant mice were compared. At 2 weeks, OPN and CD44 mRNA synthesis
was significantly elevated in mutants already displaying cardiac lesions. Mutants
without pathology showed wild-type expression levels. At 8 and 12 weeks, all mutant
hearts showed fibrotic alterations. The OPN and CD44 mRNA synthesis was higher in
the mutant than in the wildtype. OPN protein was localized exclusively in necrotic
cardiomyocytes. CD44+ cells were primarily localized in fibrotic lesions with necrotic
cardiomyocytes. The highest CD44+ cell density was found in lesions of 2- and 4-week-old
mutants. Later, CD44+ cell density declined, but did not reach wild-type levels. Staining
of serial sections with the immune cell marker CD45 implies that a high proportion
of the CD44+ cells are immune cells. In conclusion, in DSG2 mutant mice cardiac OPN
expression is associated with the onset of cardiac necrosis and fibrosis and the perpetuation
of this process. This is in accordance with observations reported for desmin -/- mice
(Mavroidis et al., 2002). In addition, CD44+/CD45+ cells are involved in the acute
and chronic phases of the cardiomyopathy.
DeGrendele HC, Estess P, Picker LJ, Siegelman MH (1996) CD44 and its ligand hyaluronate
mediate rolling under physiologic flow: a novel lymphocyte-endothelial cell primary
adhesion pathway. Exp Med 183:1119–1130
Krusche CA, Holthöfer B, Hofe V, van de Sandt AM, Eshkind L, Bockamp E, Merx MW, Kant
S, Windoffer R, Leube RE (2011) Desmoglein 2 mutant mice develop cardiac fibrosis
and dilation. Basic Res Cardiol 106:617–633
Matsui Y, Jia N, Okamoto H, Kon S, Onozuka H, Akino M, Liu L, Morimoto J, Rittling
SR, Denhardt D, Kitabatake A, Uede T (2004) Role of osteopontin in cardiac fibrosis
and remodeling in angiotensin II-induced cardiac hypertrophy. Hypertension 43:1195–1201
Mavroidis M, Capetanaki Y (2002) Extensive induction of important mediators of fibrosis
and dystrophic calcification in desmin-deficient cardiomyopathy. Am J Pathol 160:943–952
Okamoto H, Imanaka-Yoshida K (2011) Matricellular proteins: new molecular targets
to prevent heart failure. Cardiovasc Ther [Epub ahead of print]
Renault MA, Robbesyn F, Réant P, Douin V, Daret D, Allières C, Belloc I, Couffinhal
T, Arnal JF, Klingel K, Desgranges C, Dos Santos P, Charpentier F, Gadeau AP (2010)
Osteopontin expression in cardiomyocytes induces dilated cardiomyopathy. Circ Heart
Fail 3:431–439
Weber GF, Ashkar S, Glimcher MJ, Cantor H (1996) Receptor–ligand interaction between
CD44 and osteopontin (Eta-1). Science 271:509–512
P 6 — Desmoglein 2-mutant mice develop dilated cardiomyopathy without changes in the
protein synthesis of the arm-repeat domain proteins plakoglobin, plakophilin 2, and
β-catenin
Sebastian Kant, Claudia A. Krusche, Rudolf E. Leube
Institute of Molecular and Cellular Anatomy, Medical Faculty, RWTH Aachen University,
Aachen, Germany
skant@ukaachen.de; ckrusche@ukaachen.de; rleube@ukaachen.de
Desmosomal proteins are important intercalated disc (ID) components coupling cardiomyocytes.
In humans, mutations of desmosomal proteins have been implicated in arrhythmogenic
right ventricular cardiomyopathy (ARVC) and also in dilated cardiomyopathy (DCM),
which are both characterized by fibrosis and arrhythmia (Awad et al. 2008; Posch et
al. 2008; Basso et al. 2008; Marcus et al. 2010). To investigate the pathomechanism
of desmosome-related cardiomyopathy, we developed mice carrying a deletion in the
extracellular domains of the desmosomal cadherin desmoglein 2 (Dsg2). As expected,
these mice develop cardiomyopathy with dilation, pronounced fibrosis and arrhythmia.
It has been suggested that alterations in the ID localization of the plaque protein
plakoglobin are reliable diagnostic criteria for ARVC, with important implications
for its pathogenesis occurring in concert with the related arm-repeat proteins plakophilin
2 and β-catenin (Garcia-Gras et al. 2006; Asimaki et al. 2009; Fabritz et al. 2011).
We therefore examined the protein level and distribution of these polypeptides in
our mouse model. For comparison, we studied the synthesis of desmoplakin and N-cadherin.
All of these molecules are localized to the ID in the wildtype. Protein synthesis
of wild-type and mutated mouse hearts was quantified by immunoblotting, revealing
a reduction of the mutant Dsg2 but no changes of the other polypeptides. To examine
the distribution of the respective polypeptides in mutant heart tissue, semiquantitative
immunohistology was performed at different stages of disease development and in different
areas in relation to the fibrotic lesions. Except for Dsg2, all proteins still localized
to the ID at the same stoichiometry as in the wildtype. We conclude that down-regulation
or mislocalization of plakoglobin and other arm ID proteins is not obligatory for
desmosome-dependent cardiomyopathy.
Asimaki A, Tandri H, Huang H, Halushka MK, Gautam S, Basso C, Thiene G, Tsatsopoulou
A, Protonotarios N, McKenna WJ,Calkins H, Saffitz JE (2009) A new diagnostic test
for arrhythmogenic right ventricular cardiomyopathy. N Engl J Med 360:1075–1084
Awad MM, Calkins H, Judge DP (2008) Mechanisms of disease: molecular genetics of arrhythmogenic
right ventricular dysplasia/cardiomyopathy. Nat Clin Pract Cardiovasc Med. 5:258–267
Basso C, Ronco F, Marcus F, Abudureheman A, Rizzo S, Frigo AC, Bauce B, Maddalena
F, Nava A, Corrado D, Grigoletto F, Thiene G (2008) Quantitative assessment of endomyocardial
biopsy in arrhythmogenic right ventricular cardiomyopathy/dysplasia: an in vitro validation
of diagnostic criteria. Eur Heart J 29:2760–2771
Fabritz L, Hoogendijk MG, Scicluna BP, van Amersfoorth SC, Fortmueller L, Wolf S,
Laakmann S, Kreienkamp N, Piccini I,Breithardt G, Noppinger PR, Witt H, Ebnet K, Wichter
T, Levkau B, Franke WW, Pieperhoff S, de Bakker JM, Coronel R, Kirchhof P (2011) Load-reducing
therapy prevents development of arrhythmogenic right ventricular cardiomyopathy in
plakoglobin-deficient mice. J Am Coll Cardiol 57:740–750
Garcia-Gras E, Lombardi R, Giocondo MJ, Willerson JT, Schneider MD, Khoury DS, Marian
AJ (2006) Suppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin
recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy. J Clin
Invest 116:2012–2021
Marcus FI, McKenna WJ, Sherrill D, Basso C, Bauce B, Bluemke DA, Calkins H, Corrado
D, Cox MG, Daubert JP, Fontaine G, Gear K, Hauer R, Nava A, Picard MH, Protonotarios
N, Saffitz JE, Sanborn DM, Steinberg JS, Tandri H, Thiene G, Towbin JA, Tsatsopoulou
A, Wichter T, Zareba W (2010) Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia:
proposed modification of the Task Force Criteria. Eur Heart J 31:806–814
Posch MG, Posch MJ, Geier C, Erdmann B, Mueller W, Richter A, Ruppert V, Pankuweit
S, Maisch B, Perrot A, Buttgereit J, Dietz R, Haverkamp W, Özcelik C (2008) A missense
variant in desmoglein-2 predisposes to dilated cardiomyopathy. Mol Genet Metab 95:74–80
P 7 — Ultrastructural changes in hearts of desmoglein 2-mutant mice
Sabine Eisner, Claudia A. Krusche, Sebastian Kant and Rudolf E. Leube
Institute of Molecular and Cellular Anatomy, Medical Faculty, RWTH Aachen University,
Aachen, Germany
ckrusche@ukaachen.de; rleube@ukaachen.de
Mice carrying a deletion of the extracellular EC1/EC2-domains of the desmosomal cadherin
desmoglein 2 develop dilated cardiomyopathy with arrhythmia and fibrosis (Krusche,
Holthöfer et al. 2011). The mutant desmoglein 2 is still targeted to the intercalated
disc region together with the other desmosomal proteins, albeit at reduced amounts
(Krusche, Holthöfer et al. 2011). This suggests that altered adhesion may be responsible
for initiation of the disease process upon continued mechanical stress. To examine
this idea, cardiomyocyte ultrastructure was examined. We find that, in contrast to
the wild type, prominent desmosomes are rather scarce. Widening of the intercellular
cleft occurs with complete dissociation at later time points. In addition, sarcomeric
structure is disturbed, starting with altered Z-discs. At later disease stages, mitochondria
are swollen and multiple lamellar bodies are found in the cytoplasm. Finally, calcifying
necrosis of cardiomyocytes and substitution by connective tissue is observed. Taken
together, the electron microscopic data support the notion that the mutant desmoglein
2 leads to reduced adhesion in the intercalated disc region, which then leads to secondary
changes in sarcomeric structure and cell viability, resulting in necrotic cell death
and fibrosis.
Krusche CA, Holthöfer B, Hofe V, van de Sandt AM, Eshkind L, Bockamp E, Merx MW, Kant
S, Windoffer R, Leube RE (2011) Desmoglein 2 mutant mice develop cardiac fibrosis
and dilation. Basic Res Cardiol 106:617–633
P 8 — The adhering junctions of mammalian valvular interstitial cells: characterization
of fetal and adult heart valves in situ and in culture
Mareike Barth1*, Payam Akhyari2, Artur Lichtenberg2, Werner W. Franke1
(1) Helmholtz Group for Cell Biology, German Cancer Research Center, Im Neuenheimer
Feld 280, D-69120 Heidelberg, Germany
(2) Department of Cardiovascular Surgery, Düsseldorf University Hospital, Moorenstrasse
5, D-40225 Düsseldorf, Germany
*present address: Institute for Pharmacology and Clinical Pharmacology, Düsseldorf
University Hospital, Universitätsstraße 1, D-40225 Düsseldorf, Germany
Mareike.Barth@uni-duesseldorf.de; w.franke@dkfz.de
Tissue-engineered heart valves are in high demand in cardiovascular surgery. Despite
remarkable recent progress in the design and preparation of artificial valve scaffolds
or of scaffolds seeded with certain kinds of cells in vitro, cell and molecular biological
knowledge about valvular interstitial cells (VICs), i.e., the cells originally populating
the heart valve, is astonishingly limited, in particular with respect to their special
cell–cell junctions.
Using cell biological, biochemical, and immunofluorescence microscopy methods as well
as (immuno-)electron microscopy, we have characterized the adhering junctions of VICs
of human, bovine, and ovine origin in situ and after proliferation in cell culture.
These junctions are of the adherens junction (AJ) type, as demonstrable by electron
microscopy, and are similar to those found in other mesenchymal tissues. They are
composed of the transmembrane glycoproteins N-cadherin and cadherin-11 and the cytoplasmic
plaque proteins α- and β- catenin, plakoglobin and p120ctn. Desmosomal proteins are
absent from adult VICs in situ. Surprisingly, however, VICs in 2-D culture rather
rapidly acquire an additional plaque protein, the desmosomal protein plakophilin-2
(Barth et al. 2009) which, however, recently has also been noted to occur as a novel
acquisition in the AJ plaques of diverse malignantly transformed mesenchymal cells
or other cells with increased proliferation rates (Rickelt et al., 2009), cardiax
myxomata included (Rickelt et al. 2010). This quite alarming AJ alteration, however,
has been shown to be reversible in situ when these VICs are grown in a 3D-environment
composed of artificial or decellularized heart valve scaffolds, mimicking the interior
of native heart valves, as well as in surgically implanted valve replacement structures.
In pathologically altered heart valve tissues such as papillary fibroelastoma or myxomatous
degenerated heart valves, plakophilin-2 has generally been found to be absent from
the AJs present (Barth 2011).
Fetal heart valves of not only human, but also of porcine and ovine origin surprisingly
show — besides the ensemble of AJ proteins known to occur in VICs of adult valves
— also the very frequent, near-regular occurrence of the additional plaque protein
plakophilin-2 in their AJs, both in situ as well as in 2-D cultures. Remarkably, here
not only VICs show the additional plakophilin-2 but also endothelial cells of the
endocardium covering the heart valve leaflet. Therefore, a possible role for plakophilin-2
as a marker for proliferatively active mesenchymal cells present in fetal VICs as
well as in 2-D cultures of adult VICs is discussed.
Barth M (2011) The cell and molecular biological characterization of cell-cell junctions
in mammalian heart valves. PhD Thesis. Faculty of Biosciences, University of Heidelberg,
Germany. 161 pp
Barth M, Schumacher H, Kuhn C, Akhyari P, Lichtenberg A, Franke WW (2009) Cordial
connections: the molecular ensemble and the structures of the adhering junctions connecting
interstitial cells of cardiac valves in situ and in cell culture. Cell Tissue Res
337:63–77
Rickelt S, Winter-Simanowski S, Noffz E, Kuhn C, Franke WW (2009) Upregulation of
plakophilin-2 and its acquisition to adherens junctions identifies a novel molecular
ensemble of cell–cell-attachment characteristic for transformed mesenchymal cells.
Int J Cancer 125:2036–2048
Rickelt S, Rizzo S, Dörflinger Y, Zentgraf H, Basso C, Gerosa G, Thiene G, Moll R,
Franke WW (2010) A novel kind of tumor type-characteristic junction: plakophilin-2
as a major protein of adherens junctions in cardiac myxomata. Mod Pathol 23:1429–1437
P 9 — The protein myozap, a major constitutive plaque component of the composite junctions
(areae compositae) of the myocardiac intercalated disks, is also a major and widespread
protein in the cell–cell junctions of endothelial cells of blood and lymph vessels
Sebastian Pieperhoff1,2,*, Steffen Rickelt1,3, Caecilia Kuhn1,3, Ralf Zimbelmann1,
Hans W Heid1, Heiderose Schumacher1, Stefanie Winter-Simanowski1, Norbert Frey4, Werner
W. Franke1,3
(1) Helmholtz Group Cell Biology, German Cancer Research Center (DKFZ), Heidelberg,
Germany
(2) Department of Zoology and Faculty of Land and Food Systems, University of British
Columbia, Vancouver, BC, Canada
(3) Progen Biotechnik GmbH, Heidelberg, Germany
(4) Department of Cardiology and Angiology, University Hospital Schleswig-Holstein,
Campus Kiel, Germany
*present address: Centre for Cardiovascular Science, The Queen’s Medical Research
Institute, University of Edinburgh, Scotland, UK
s.pieperhoff@gmail.com; w.franke@dkfz.de
The protein myozap, a 54-kDa polypeptide which is not a member of any of the known
junctional protein multigene families, has been identified as a major constituent
of the plaques of the composite junctions in the intercalated disks (IDs) connecting
cardiomyocytes (Seeger et al. 2010). Using highly sensitive and specific antibodies,
we have detected myozap also in cytoplasmic plaques of the adherens junctions (AJs)
connecting endothelial cells of the mammalian blood and lymphatic vascular system,
including the desmoplakin-containing complexus adhaerentes of the virgultar cells
of lymph node sinus, and in cultured endothelial cells. In light- and electronmicroscopic
immunolocalization experiments, we show that myozap colocalizes with several proteins
of desmosomal plaques as well as with AJ-specific molecules, including VE- and N-cadherin.
In biochemical analyses of myozap, immunoprecipitation experiments have revealed desmoplakin,
plakophilin-2, protein ZO-1 and plectin as the most prominent complex partners. We
conclude that myozap is a general component of cellular junctions in the cardiovascular
system, suggesting that this protein not only serves a specific role in the heart
IDs, but also functions in the vascular system (for details see Pieperhoff et al.
2011).
Seeger TS, Franke D, Rohr C, Will R, Grund C, Koegel M, Franke WW, Katus HA, Olson
EN, Frey N (2010) Myozap, a novel intercalated disc protein, activates serum response
factor-dependent signaling and is required to maintain cardiac function in vivo. Circ
Res 106:880–890
Pieperhoff S, Heid H, Claycomb WC, Zimbelmann R, Kuhn C, Winter-Simanowski S, Kuhn
C, Frey N, Franke WW (2011) The plaque protein myozap defines novel major categories
of cardiovascular adhering junctions. J Cell Mol Med 13 Oct [Epub ahead of print]
P 10 — Cell–cell junctions out of the textbook scheme: special structures in their
own right
Steffen Rickelt1,2, Sebastian Pieperhoff1,3, Caecilia Kuhn2, Roland Moll4, Werner
W. Franke1,2
(1) Helmholtz Group for Cell Biology, German Cancer Research Center, Heidelberg, Germany
(2) Progen Biotechnik, Heidelberg
(3) Centre for Cardiovascular Science, The Queen´s Medical Research Institute, University
of Edinburgh, Scotland, UK
(4) Institute of Pathology, Philipps University Marburg, Germany
s.rickelt@dkfz.de; w.franke@dkfz.de
According to the prevailing textbook dogma there are two — and only two — distinct
types of cell–cell connecting, Ca2+-dependent, plaque-bearing adhering junctions (AJs):
the microfilament-associated AJs, including the zonula adhaerens and puncta adhaerentia,
and the intermediate filament (IF)-anchoring desmosomes (maculae adhaerentes), most
prominent for epithelial cells. The molecular composition of both kinds of AJs has
been — almost completely — elucidated, and the specific antibodies are widely used
in diagnostic pathology and in developmental biology. Using immunocytochemical, electron,
and immunoelectron microscopical methods, we have revealed that in addition to these
"textbook categories" of junctions a broad range of other junctions exists. These
are the tiny puncta adhaerentia minima, the taproot junctions (manubria adhaerentia),
the plakophilin-2-containing AJs of mesenchymal or mesenchymally derived cell types,
including malignantly transformed ones, as well as the composite junctions (areae
compositae) of the mature mammalian myocardium, the cortex adhaerens of the eye lens,
the interdesmosomal "sandwich" or "stud" junctions in the subapical layers of stratified
epithelia (including tumors derived therefrom), and the complexus adhaerentes of the
endothelial and virgultar cells of the vascular system. These junctions cannot be
subsumed under one of the major categories mentioned above but represent special structures
in their own right, appear to serve special functions, and can may provide new markers
for cell typing.
Franke WW, Borrmann CM, Grund C, Pieperhoff S (2006) The area composita of adhering
junctions connecting heart muscle cells of vertebrates. I. Molecular definition in
intercalated disks of cardiomyocytes by immunoelectron microscopy of desmosomal proteins.
Eur J Cell Biol 85:69–82
Franke WW, Rickelt S, Barth M, Pieperhoff S (2009) The junctions that don't fit the
scheme: special symmetrical cell–cell junctions of their own kind. Cell Tissue Res
338:1–17
Moll R, Sievers E, Hämmerling, Schmidt A, Barth M, Kuhn C, Grund C, Hofmann I, Franke
WW (2009) Endothelial and virgultar cell formations in the mammalian lymph node sinus:
endothelial differentiation morphotypes characterized by a special kind of junction
(complexus adhaerens). Cell Tissue Res 335:109–141
Pieperhoff S, Barth M, Rickelt S, Franke WW (2010) Desmosomal molecules in and out
of adhering junctions: normal and diseased states of epidermal, cardiac and mesenchymally
derived cells. Dermatol Res Pract 2010: 139167
Rickelt S, Rizzo S, Dörflinger Y, Zentgraf H, Basso C, Gerosa G, Thiene G, Moll R,
Franke WW (2010) A novel kind of tumor type-characteristic junction: plakophilin-2
as a major protein of adherens junctions in cardiac myxomata. Mod Pathol 23:1429–1437
P 11 — Telocyte connections in the heart
Mihaela Gherghiceanu, Laurentiu M. Popescu
Department of Advanced Studies, ‘Victor Babeş’ National Institute of Pathology, Bucharest,
Romania
mgherghiceanu@yahoo.com
The heart is a heterogeneous organ composed of different types of cardiomyocytes,
capillaries, nerves, and a large variety of interstitial cells. Among interstitial
cells, telocytes (TCs), cells with telopodes (Tp), seem to be particularly involved
in intercellular communication (Popescu and Faussone-Pellegrini 2010). Electron microscopy
(EM) studies have shown that TCs are interconnected, and have close apposition but
not conventional junctions (Franke et al. 2009) with cardiomyocytes (CM) and other
interstitial cells. In order to detail the architecture of the heterocellular and
homocellular junctions of TCs in mouse heart we performed electron tomography (ET).
EM and ET showed that Tp are coupled each other by different types of homocellular
junctions: puncta adhaerentia minima, processus adhaerentes and manubria adhaerentia.
In addition, TCs establish heterocellular junctions with adult cardiomyocytes (Gherghiceanu
and Popescu 2011), cardiomyocyte progenitors or putative stem cells (Gherghiceanu
and Popescu 2010). EM study also showed that TCs establish small atypical junctions,
point contacts, with macrophages or with Schwann cells. Ultrastructural analysis showed
that TCs form an interstitial network by homocellular junctions, and link all cardiac
cells. We assume that TCs play a significant role in cardiac physiology as structural
support for long-distance heterocellular signaling.
Franke WW, Rickelt S, Barth M, Pieperhoff S (2009) The junctions that don't fit the
scheme: special symmetrical cell–cell junctions of their own kind. Cell Tissue Res
338:1–17
Gherghiceanu M, Popescu LM (2010) Cardiomyocyte precursors and telocytes in epicardial
stem cell niche: electron microscope images. J Cell Mol Med 14:871–877
Gherghiceanu M, Popescu LM (2011) Heterocellular communication in the heart: electron
tomography of telocyte–myocyte junctions. J Cell Mol Med 15:1005–1011
Popescu LM, Faussone-Pellegrini MS (2010) Telocytes — a case of serendipity: the winding
way from interstitial cells of Cajal (ICC), via interstitial Cajal-like cells (ICLC)
to telocytes. J Cell Mol Med 14:729–740
P 12 — Intermediate filaments are essential for the structure and function of the
cardiac conduction system (sinus node)
Nikos Athanasiadis, Dimitris Chaniotis, Pavlos Rigas, Ioanna Kostavsili, Erene Skaliora,
Yassemi Capetanaki, Costas Davos, Manolis Mavroidis
Biomedical Research Foundation, Academy of Athens, Greece
emavroeid@bioacademy.gr
In mammals, each heartbeat is triggered by a single electrical impulse generated in
the "pacemaker region" of the sinus node, and then propagated to the atrial and ventricular
myocytes. In the present study, we have tried to elucidate how perturbations of the
intermediate filament (IF) cytoskeleton lead to cardiac conduction system dysfunction
and arrhythmias. As is known, the cardiac phenotype of mutations in the muscle specific
IF protein desmin can involve — besides others — conduction defects such as AV block
and ARVD/C. In wild-type sinus nodes, we have found that transitional cells are laterally
coupled by structures we call "lateral intercalated discs". By immunofluorescence
staining, these structures are positive for desmoplakin, ‚-catenin and desmin. These
structures are also evident by electron microscopy. Surprisingly, analysis of sinus
node isolated from desmin-null mice has indicated that "lateral intercalated discs"
are diminished or absent in these mice. In addition, analysis of electrical activity
(field potential recordings) of isolated sinus nodes has revealed that there is a
50 % reduction in spike amplitude and a 40 % increase in discharge frequency in desmin-null
mice compared to the wild-type one. These results support the hypothesis that cells
in the desmin-null sinus node have decreased communication and coordination capacity
compared to wild type.
Analysis of sinus nodes from human healthy individuals who unfortunately died young
revealed that these "lateral intercalated disks" are also present in transitional
cells, and we have found (by immunofluorescence) that desmoplakin is a major constituent
of the subsarcolemmal cytoskeleton. Desmoplakin forms a lattice at the subsarcolemmal
level (costameres), possibly providing a scaffold with very important functions for
the human conduction system. Sinus nodes from young individuals who died from sudden
cardiac death are under analysis as candidates with plausible perturbations in these
elements.
P 13 — Deleterious effects of the
TMEM43
mutation p.S358L found in a German family with arrhythmogenic right ventricular cardiomyopathy
and sudden cardiac death
Baerbel Klauke1, Carolin Baecker1, Joerg Muesebeck2, Eric Schulze-Bahr3, Désirée Gerdes1,
Anna Gaertner1, Hendrik Milting1
(1) Heart and Diabetes Center NRW, Erich & Hanna Klessmann-Institute for Cardiovascular
Research & Development, Bad Oeynhausen, Germany
(2) University of Bremen, Center of Human Genetics, Bremen, Germany
(3) University Clinic Münster, Institute for Genetics of Heart Diseases, Münster,
Germany
bklauke@hdz-nrw.de; hmilting@hdz-nrw.de
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by loss of
ventricular myocardium, which might lead to terminal heart failure or sudden cardiac
death (SCD). ARVC is a genetically heterogeneous disorder. The purpose of this study
was to determine the prevalence of ARVC related TMEM43 gene mutations in 22 ARVC patients.
We screened the entire TMEM43 gene of 22 ARVC index patients previously genotyped
for desmosomal (DSG2, DSC2, PKP2, JUP, DSP) and DES gene mutations (Klauke et al.
2010) by denaturing high pressure liquid chromatography (dHPLC) and Sanger sequencing.
We have identified a 70-year-old female with borderline ARVC (Sen-Chowdhry et al.
2010) as carrier of the previously identified TMEM43 c. 1073C>T (p.S358L) mutation
(Merner et al. 2008; Christensen et al. 2011). Cosegregation with the ARVC phenotype
within the family has clearly been demonstrated. The female carriers of p.S358L presented
a rather mild arrhythmogenic phenotype, whereas three male relatives died in the second
to third decade by sudden cardiac death. In samples of additional 37 ARVC patients,
22 DCM patients, and 382 healthy controls, the mutation was not identified. Although
the allele frequency appears to be low in German ARVC patients, TMEM43 should be included
in molecular genetic testing of ARVC patients.
Christensen AH, Andersen CB, Tybjærg-Hansen A, Haunso S, Svendsen JH (2011) Mutation
analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right
ventricular cardiomyopathy. Clin Genet 80:256–264
Klauke B, Kossmann S, Gaertner A, Brand K, Stork I, Brodehl A, Dieding M, Wahlhorn
V, Anselmetti D, Gerdes D, Bohms B, Schulz U, zu Knyphausen E, Vorgerd M, Gummert
J, Milting H (2010) De novo desmin mutation N116S is associated with arrhythmogenic
right ventricular cardiomyopathy. Hum Mol Genet 19:4595–4607
Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion
C, Ramadanova K, Thierfelder L, McKenna W (2008) Arrhythmogenic right ventricular
cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a
missense mutation in the TMEM43 gene. Am J Hum Genet 82: 809–821
Sen-Chowdhry S, Morgan RD, Chambers JC, McKenna WJ (2010) Arrhythmogenic cardiomyopathy:
etiology, diagnosis, and treatment. Annu Rev Med 61: 233–253
P 14 — Myocardial transcriptome analysis of human arrhythmogenic right ventricular
cardiomyopathy (ARVC)
Anna Gaertner1, Patrick Schwientek2, Peter Ellinghaus3, Holger Summer3, Stefan Golz3,
Astrid Kassner1, Uwe Schulz1, Jan Gummert1, Hendrik Milting1
(1) Heart and Diabetes Center NRW, Erich & Hanna Klessmann-Institute for Cardiovascular
Research & Development, Georgstr. 11, D-32545 Bad Oeynhausen, Germany
(2) Center for Biotechnology, Bielefeld University, Universitätsstr. 27, D-33615 Bielefeld,
Germany
(3) Bayer Pharma AG, Global Drug Discovery, D-42096 Wuppertal, Germany
AGaertner@hdz-nrw.de; hmilting@hdz-nrw.de
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy
primarily of the right ventricle (Basso et al. 1996; Marcus et al. 1982; Thiene et
al. 1988). Five of the causal genes are coding for desmosomal proteins (Gerull et
al. 2004; McKoy et al. 2000; Norgett et al. 2000; Sen-Chowdhry et al. 2005; Syrris
et al. 2007). Though electron microscopy of endomyocardial biopsies of ARVC patients
revealed remodelling of intercalated discs and abnormal desmosomes, the molecular
pathomechanisms are largely unknown (Basso et al. 2006).
Paired myocardial samples from the left (LV) and right ventricles (RV) were obtained
from six non-failing (NF) donor hearts, six ARVC patients and seven patients with
idiopathic dilated cardiomyopathy (DCM). The samples were analyzed by Affymetrix HG-U133
Plus 2.0 arrays for differential transcription. The analysis of our data by unsupervised
cluster analyses and t-tests indicated that ARVC is a cardiomyopathy, which is not
restricted to the RV. Unsupervised PCA of the ARVC subgroup revealed a common cluster
for LV and RV samples of patients with desmosomal gene mutations. Surprisingly, in
the LV of ARVC patients the gene expression of Plakophilin-2 was shown to be up-regulated,
whereas expression of Desmocollin-2 was down-regulated. No transcriptional regulation
of these genes was observed in the RV of ARVC patients in our study. None of the other
ARVC-related desmosomal genes was regulated in RV or LV of ARVC patients.
Our study is the first analysis of specific ARVC-related RV and LV gene expression
patterns in terminally failing human hearts. It offers further insight into the disease
mechanisms of ARVC and might probably reveal further candidate genes relevant for
molecular genetics of ARVC.
Basso C, Czarnowska E, Della Barbera M, Bauce B, Beffagna G, Wlodarska EK, Pilichou
K, Ramondo A, Lorenzon A, Wozniek O, Corrado D, Daliento L, Danieli GA, Valente M,
Nava A, Thiene G, Rampazzo A (2006) Ultrastructural evidence of intercalated disc
remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy
investigation on endomyocardial biopsies. Eur Heart J 27:1847–1854
Basso C, Thiene G, Corrado D, Angelini A, Nava A, Valente M (1996) Arrhythmogenic
right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis? Circulation
94:983–991
Gerull B, Heuser A, Wichter T, Paul M, Basson CT, McDermott DA, Lerman BB, Markowitz
SM, Ellinor PT, MacRae CA, Peters S, Grossmann KS, Drenckhahn J, Michely B, Sasse-Klaassen
S, Birchmeier W, Dietz R, Breithardt G, Schulze-Bahr E, Thierfelder L (2004) Mutations
in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular
cardiomyopathy. Nat Genet 36:1162–1164
Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, Basson CT, Lerman
BB, Sasse-Klaassen S, Thierfelder L, MacRae CA, Gerull B (2006) Mutant desmocollin-2
causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet 79:1081–1088
Marcus FI, Fontaine GH, Guiraudon G, Frank R, Laurenceau JL, Malergue C, Grosgogeat
Y (1982) Right ventricular dysplasia: a report of 24 adult cases. Circulation 65:384–398
McKoy G, Protonotarios N, Crosby A, Tsatsopoulou A, Anastasakis A, Coonar A, Norman
M, Baboonian C, Jeffery S, McKenna WJ (2000) Identification of a deletion in plakoglobin
in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and
woolly hair (Naxos disease). Lancet 355:2119–2124
Norgett EE, Hatsell SJ, Carvajal-Huerta L, Cabezas JC, Common J, Purkis PE, Whittock
N, Leigh IM, Stevens HP, Kelsell DP (2000) Recessive mutation in desmoplakin disrupts
desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy,
woolly hair and keratoderma. Hum Mol Genet 9:2761–2766
Sen-Chowdhry S, Syrris P, McKenna WJ (2005) Genetics of right ventricular cardiomyopathy.
J Cardiovasc Electrophysiol 16:927–935
Syrris P, Ward D, Asimaki A, Evans A, Sen-Chowdhry S, Hughes SE, McKenna WJ (2007)
Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype–phenotype
characterization of familial disease. Eur Heart J 28:581–588
Thiene G, Nava A, Corrado D, Rossi L, Pennelli N (1988) Right ventricular cardiomyopathy
and sudden death in young people. N Engl J Med 318:129–133
P 15 — Alpha-catenin recruits vinculin to cadherin junctions in a force-dependent
manner: does it play a role during morphogenesis of the heart?
Esteban Hoijman1, Iris Blonk1, Jeroen Bakkers1, Holger Rehmann2, Johan de Rooij1
(1) Hubrecht Institute, Utrecht, The Netherlands
(2) University Medical Center Utrecht, Utrecht, The Netherlands
e.hoijman@hubrecht.eu
Several animal models have shown that proteins of the cell–cell junctions (CCJs) such
as VE-cadherin, alpha-catenin and vinculin are important for heart development. Next
to their well-known structural role, these CCJs mediated by cadherins are also mechanosensitive.
The exact role of the cadherin complex proteins during heart morphogenesis is not
well-understood and, in particular, the role of mechanotransduction on this process
is unknown.
Force-dependent recruitment of vinculin to CCJs is essential for cadherin mechanosensing.
To determine the role of mechanotransduction in heart development, we aimed to block
this recruitment. As it was proposed that vinculin recruitment depends on its binding
to alpha-catenin, we replaced the vinculin interaction domain of alpha-catenin with
the homologous domain from vinculin (its closest homolog), obtaining an alpha-catenin/vinculin
hybrid. This construct fully restored the formation of CCJs in several alpha-catenin
negative cell lines, and actomyosin contraction was no longer able to induce the recruitment
of vinculin to the junctions in these cells. Our ultimate goal is to block the alpha-catenin/vinculin
interaction in vivo during zebrafish heart development. To this end, we started analyzing
the heart phenotypes produced by injection of vinculin and alpha-catenin morpholinos.
Both of these showed different defects in heart development at 24 and 48 hpf. Next,
we will test the defects caused by the specific loss of junctional vinculin, by rescuing
alpha-catenin depletion with the alpha-catenin/vinculin hybrid.
In conclusion, the results in vitro suggest that force-dependent recruitment of vinculin
to CCJs can be specifically prevented by an alpha-catenin mutant that does not perturb
CCJs per se. This allows us to design in vivo experiments to determine the role of
cadherin mechanosensing during heart morphogenesis.