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      Generation of a Functioning and Self‐Renewing Diaphragmatic Muscle Construct

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          Abstract

          Surgical repair of large muscular defects requires the use of autologous graft transfer or prosthetic material. Naturally derived matrices are biocompatible materials obtained by tissue decellularization and are commonly used in clinical practice. Despite promising applications described in the literature, the use of acellular matrices to repair large defects has been only partially successful, highlighting the need for more efficient constructs. Scaffold recellularization by means of tissue engineering may improve not only the structure of the matrix, but also its ability to functionally interact with the host. The development of such a complex construct is challenging, due to the complexity of the native organ architecture and the difficulties in recreating the cellular niche with both proliferative and differentiating potential during growth or after damage. In this study, we tested a mouse decellularized diaphragmatic extracellular matrix (ECM) previously described by our group, for the generation of a cellular skeletal muscle construct with functional features. The decellularized matrix was stored using different conditions to mimic the off‐the‐shelf clinical need. Pediatric human muscle precursors were seeded into the decellularized scaffold, demonstrating proliferation and differentiation capability, giving rise to a functioning three‐dimensional skeletal muscle structure. Furthermore, we exposed the engineered construct to cardiotoxin injury and demonstrated its ability to activate a regenerative response in vitro promoting cell self‐renewal and a positive ECM remodeling. Functional reconstruction of an engineered skeletal muscle with maintenance of a stem cell pool makes this a promising tool toward future clinical applications in diaphragmatic regeneration. stem cells translational medicine 2019;8:858&869

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          Most cited references61

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          Human ES- and iPS-derived myogenic progenitors restore DYSTROPHIN and improve contractility upon transplantation in dystrophic mice.

          A major obstacle in the application of cell-based therapies for the treatment of neuromuscular disorders is obtaining the appropriate number of stem/progenitor cells to produce effective engraftment. The use of embryonic stem (ES) or induced pluripotent stem (iPS) cells could overcome this hurdle. However, to date, derivation of engraftable skeletal muscle precursors that can restore muscle function from human pluripotent cells has not been achieved. Here we applied conditional expression of PAX7 in human ES/iPS cells to successfully derive large quantities of myogenic precursors, which, upon transplantation into dystrophic muscle, are able to engraft efficiently, producing abundant human-derived DYSTROPHIN-positive myofibers that exhibit superior strength. Importantly, transplanted cells also seed the muscle satellite cell compartment, and engraftment is present over 11 months posttransplant. This study provides the proof of principle for the derivation of functional skeletal myogenic progenitors from human ES/iPS cells and highlights their potential for future therapeutic application in muscular dystrophies. Copyright © 2012 Elsevier Inc. All rights reserved.
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            Adult satellite cells and embryonic muscle progenitors have distinct genetic requirements.

            Myogenic potential, survival and expansion of mammalian muscle progenitors depend on the myogenic determinants Pax3 and Pax7 embryonically, and Pax7 alone perinatally. Several in vitro studies support the critical role of Pax7 in these functions of adult muscle stem cells (satellite cells), but a formal demonstration has been lacking in vivo. Here we show, through the application of inducible Cre/loxP lineage tracing and conditional gene inactivation to the tibialis anterior muscle regeneration paradigm, that, unexpectedly, when Pax7 is inactivated in adult mice, mutant satellite cells are not compromised in muscle regeneration, they can proliferate and reoccupy the sublaminal satellite niche, and they are able to support further regenerative processes. Dual adult inactivation of Pax3 and Pax7 also results in normal muscle regeneration. Multiple time points of gene inactivation reveal that Pax7 is only required up to the juvenile period when progenitor cells make the transition into quiescence. Furthermore, we demonstrate a cell-intrinsic difference between neonatal progenitor and adult satellite cells in their Pax7-dependency. Our finding of an age-dependent change in the genetic requirement for muscle stem cells cautions against inferring adult stem-cell biology from embryonic studies, and has direct implications for the use of stem cells from hosts of different ages in transplantation-based therapy.
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              Differentiation of pluripotent stem cells to muscle fiber to model Duchenne muscular dystrophy.

              During embryonic development, skeletal muscles arise from somites, which derive from the presomitic mesoderm (PSM). Using PSM development as a guide, we establish conditions for the differentiation of monolayer cultures of mouse embryonic stem (ES) cells into PSM-like cells without the introduction of transgenes or cell sorting. We show that primary and secondary skeletal myogenesis can be recapitulated in vitro from the PSM-like cells, providing an efficient, serum-free protocol for the generation of striated, contractile fibers from mouse and human pluripotent cells. The mouse ES cells also differentiate into Pax7(+) cells with satellite cell characteristics, including the ability to form dystrophin(+) fibers when grafted into muscles of dystrophin-deficient mdx mice, a model of Duchenne muscular dystrophy (DMD). Fibers derived from ES cells of mdx mice exhibit an abnormal branched phenotype resembling that described in vivo, thus providing an attractive model to study the origin of the pathological defects associated with DMD.
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                Author and article information

                Contributors
                m.pozzobon@irpcds.org
                m.piccoli@irpcds.org
                Journal
                Stem Cells Transl Med
                Stem Cells Transl Med
                10.1002/(ISSN)2157-6580
                SCT3
                Stem Cells Translational Medicine
                John Wiley & Sons, Inc. (Hoboken, USA )
                2157-6564
                2157-6580
                10 April 2019
                August 2019
                : 8
                : 8 ( doiID: 10.1002/sct3.2019.8.issue-8 )
                : 858-869
                Affiliations
                [ 1 ] Fondazione Istituto di Ricerca Pediatrica Città della Speranza Padova Italy
                [ 2 ] Department of Women and Children Health University of Padova Padova Italy
                [ 3 ] Department of Industrial Engineering University of Padova Padova Italy
                [ 4 ] Centre for Mechanics of Biological Materials University of Padova Padova Italy
                [ 5 ] Department of Biomedical Sciences University of Padova Padova Italy
                [ 6 ] CNR Institute for Neuroscience Padova Italy
                [ 7 ] Department of Biology University of Padova Padova Italy
                [ 8 ] Stem Cells & Regenerative Medicine Section Developmental Biology & Cancer Programme, UCL Great Ormond Street Institute of Child Health London United Kingdom
                [ 9 ] Institute of Hepatology The Foundation for Liver Research London United Kingdom
                [ 10 ] Faculty of Life Sciences & Medicine King's College London United Kingdom
                [ 11 ] Department of Surgery, Oncology, and Gastroenterology DiSCOG Orthopaedic Clinic, University of Padova Padua Italy
                [ 12 ] Laboratory of Regenerative Medicine – Cell Factory Department of Transfusion Medicine and Hematology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano Italy
                [ 13 ] Specialist Neonatal and Paediatric Surgery Great Ormond Street Institute of Child Health London United Kingdom
                Author notes
                [*] [* ]Correspondence: Martina Piccoli, Ph.D., Tissue Engineering Lab, Istituto di Ricerca Pediatrica Città della Speranza, Corso Stati Uniti 4, 35129 Padova, Italy. Telephone: 39‐049‐9640129; e‐mail: m.piccoli@ 123456irpcds.org ; or Michela Pozzobon, Ph.D., Stem Cells and Regenerative Medicine Lab, Istituto di Ricerca Pediatrica Città della Speranza, Corso Stati Uniti 4, 35129 Padova, Italy. Telephone: 39‐049‐9640126; e‐mail: m.pozzobon@ 123456irpcds.org
                Author information
                https://orcid.org/0000-0001-6211-0051
                Article
                SCT312501
                10.1002/sctm.18-0206
                6646700
                30972959
                b8c603f0-b3bd-456e-a762-8c934d040820
                © 2019 The Authors. stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 24 September 2018
                : 04 March 2019
                Page count
                Figures: 6, Tables: 0, Pages: 12, Words: 10602
                Funding
                Funded by: Fondazione Istituto di Ricerca Pediatrica Città della Speranza
                Award ID: Fondazione Cariparo‐IRP 2013–2016
                Award ID: Fondazione Cariparo‐IRP 2016–2018
                Funded by: University of Padova
                Award ID: GRIC15AIPF
                Funded by: NIHR
                Categories
                Tissue Engineering and Regenerative Medicine
                Tissue Engineering and Regenerative Medicine
                Custom metadata
                2.0
                sct312501
                August 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.6.2 mode:remove_FC converted:23.07.2019

                decellularized scaffold,extracellular matrix,diaphragm,human muscle precursor cells,recellularization

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