UCB Pharma asked Geoffrey Burnstock to propose a programme of 8 international leaders
in the glia-neuron interaction and purinergic signalling field to participate in a
meeting aimed at introducing the topic to about 30 members of the Company to consider
the therapeutic potential of purinergic signalling compounds for the treatment of
neurological disorders, including: epilepsy, neurodegenerative diseases, movement
disorders, neuroprotection, mood disorders and neuropathic pain.
Geoff Burnstock, acting as the Chairman of this 1-day meeting, held at the Château
de Limelette, Belgium, introduced the objectives of the meeting. He stressed the sophisticated
biology that was involved in drug development and the advantages of collaborations
between basic scientists, clinicians and the drug industry in bringing advances in
knowledge from basic science to application in clinical medicine for the treatment
of disease.
The morning session was devoted to the mechanisms underlying glia-neuron interactions.
Professor Philip Haydon from the Department of Neuroscience, University of Pennsylvania,
USA, led off by describing ‘The tripartite synapse: how astrocytes listen and talk
to neurons’, describing the functional as well as structural interactions between
three elements: the neuronal presynaptic component, the postsynaptic neuronal component
and the perisynaptic astrocyte.
Astrocytes are intimately associated with neurons and, through their extensive contacts
with synapses, they are able to regulate synaptic transmission. Since the discovery
of the ability of astrocytes to release chemical transmitters, a process that is termed
gliotransmission, our understanding of the dynamical regulatory roles for these glial
cells has dramatically expanded. Astrocytes are equipped with the necessary machinery
to listen and to talk to neurons. Following synaptic activity neurotransmitters acting
through glial metabotropic receptors induce glial Ca2+ signals. In turn, these Ca2+
signals can induce the release of a variety of chemical transmitters, including glutamate,
ATP and D-serine.
Using a variety of astrocyte-specific manipulations recent work has identified a variety
of physiological and pathological functions for this process of gliotransmission.
By releasing ATP, which is converted in the extracellular space to adenosine, astrocytes
exert a powerful presynaptic inhibition of synaptic transmission. Glutamate and D-serine
released from astrocytes activate neuronal N-methyl-D-aspartate (NMDA) receptors.
These glial-neuron signalling pathways regulate neuronal excitability and synaptic
transmission. When examined in vivo recent studies show that neuronal networks are
under the continuous modulatory control of the astrocyte through both purinergic and
NMDA receptor-dependent pathways. In addition to providing physiological modulatory
actions, astrocytes have the potential to contribute to neurological disorders and
psychiatric states. The contribution of gliotransmission to delayed neuronal death
was discussed.
He concluded that our understanding of brain function is changing from one in which
neuron-based electrical signals are the formal code to one in which rapid electrical
signals in neuronal networks interact with slow modulatory signals provided by glia.
The ultimate function or dysfunction of the nervous system during health and disease
is an emergent property of these neuron-glial interactions.
The next lecture was presented by Professor Andrea Volterra, from the Department of
Cell Biology and Morphology, University of Lausanne, Switzerland. His talk, entitled
‘Gliotransmission, synaptic plasticity and synaptic dysfunction’, focused on the process
of exocytosis of glutamate and other ‘gliotransmitters’ released from astrocytes and
on modes of rapid communication of glia with neighbouring cells. Using an interdisciplinary
approach, he described the mechanisms of gliotransmission in the normal brain physiology
and in brain diseases, as well as identifying signalling steps that may contribute
to novel drug targets. He discussed how glial activity follows two routes: an intracellular
one through gap junctions (connexins) and an extracellular one via release of ATP,
glutamate and serine. Astrocytes also contain a synaptic-like microvessel compartment
for uptake, storage and release of glutamate. Such gliotransmission plays a role in
synapse formation, synaptic function, adult neurogenesis and neurovascular tone.
Astrocytes control excitatory transmission and synaptic strength at hippocampal synapses
via purinergic P2Y1 receptor signalling, glutamate and tumour necrosis factor-α (TNFα).
Modulatory control in the hippocampal dentate gyrus in response to activation of P2Y1
purinoreceptors (P2Y1R) was shown and immunochemistry demonstrated that P2Y1Rs are
localised preferentially in astrocyte processes directly apposed to asymmetric synapses
in the dentate molecular layer. In hippocampal slices, activation of P2Y1R with the
selective agonist, 2-methylthioadenosine-5′-diphosphate (2-MeSADP), triggers glutamate
release. P2Y1R activation with 2-MeSADP causes increased miniature excitatory postsynaptic
currents (mEPSC) and spontaneous EPSC (sEPSC) activity in dentate granule cells (CG).
P2Y1R signalling in astrocytes activates presynaptic NMDA receptors via release of
glutamate.
Post-embedding immunogold cytochemistry showed gold particles in the extrasynaptic
portion of excitatory nerve terminals. Stimulation of astrocyte P2Y1R induces release
of TNFα in addition to glutamate. The two signalling events are correlated, as P2Y1R-evoked
glutamate release is dramatically reduced in TNFα knockout mice.
Professor Christian Steinhäuser, Director of the Institute of Cellular Neuroscience,
University of Bonn, Germany, gave a talk entitled ‘A role for astrocytes in epilepsy’.
He suggested that astrocytes may be active players in the cellular basis of hyperexcitability
and synchronization in epilepsy and other neurological diseases. The functional significance
of transmitter release from astrocytes involves modulation of the strength of excitatory
and inhibitory synaptic transmission by activating receptors and neurons. As each
astrocyte can reach thousands of synapses simultaneously, the release of gliotransmitter
may lead to synchronization of neuronal firing patterns. Epilepsy is often accompanied
by massive glial cell proliferation, even though the exact role of these cells in
seizures and epilepsy is still unclear. Not only do glial cells express various ion
channels and receptors, but they are probably functionally heterogeneous. Therefore,
a better understanding of mechanisms of glial function in brain health and disease
may offer the potential for developing novel strategies to treat epilepsy and other
brain disorders. The current anticonvulsant drugs and complementary therapies are
not sufficient to control seizures in about a third of epileptic patients. Thus, there
is an urgent need for treatments that prevent the development of epilepsy and control
it better in patients already inflicted with the disease. Despite significant advances
in different fields of neuroscience, the pathological mechanisms of epileptic disorders
remain poorly understood. An improved understanding of astrocyte biology and the involvement
of glial cells in epileptogenesis offers the potential for developing novel strategies
to treat epilepsy. Work in his laboratory had recently identified two distinct types
of cells with astroglial properties, GluR cells and GluT cells, co-existing in mouse
hippocampus. GluR cells express ionotropic glutamate receptors of the α-amino-3-hydroxy-5-methyl-4-isoxazole
propionic acid (AMPA) subtype, receive synaptic input from hippocampal neurons, and
lack functional glutamate transporters and gap junction coupling. GluT cells, in contrast,
display glutamate transporter activity, gap junction coupling, touch brain capillaries
with their endfeet, but lack ionotropic glutamate receptors. Both types of astroglial
cells are also present in the hippocampus of patients presenting with intractable
temporal lobe epilepsy (lesion-associated, non-sclerotic epilepsy). However, in patients
suffering from Ammon’s horn sclerosis, the most common type of neuropathological damage
seen in individuals with temporal lobe epilepsy, one subpopulation of these cells
(GluT-type) almost completely disappears while the remaining GluR cells undergo molecular
and functional alterations of their glutamate receptors. These findings support the
hypothesis that glial cells play a key role in the generation and/or spread of seizure
activity in human epilepsy. This deleterious effect is brought about by (1) the abundant
excitatory neurotransmitter glutamate and (2) impaired gap junction-mediated buffering
of K+ and metabolites, leading to prolonged activation of cells in the hippocampus,
a brain region crucially involved in learning, memory and emotional processing. Analyses
of more than a hundred brain specimens neurosurgically resected from epilepsy patients
were used to substantiate this intriguing new insight. The findings challenge the
common view of epileptogenesis according to which neurons are considered the prime
targets affected in this disease.
Professor Francesco Di Virgilio, from the Department of Experimental and Diagnostic
Medicine, University of Ferrara, Italy, presented the last talk of the morning session
entitled ‘Immuno-neural interaction and neuro-inflammatory diseases’. He discussed
the molecular mechanisms underlying neuro-inflammation, in particular, the two-way
communication between neurons and microglia, in which purinergic signalling (ATP and
the ionotropic ATP receptor subtype P2X7) constitutes a key pathway. Release of ATP
from neurons directly modulates microglial function, resulting in secretion of neurotrophic
factors, or, if excessive or protracted, in the release of proinflammatory mediators,
amongst which interleukin (IL)-1β and IL-18 are the cytokines most tightly controlled
by the P2X7 receptor. Conversely, purinergic stimulation of microglia via P2 receptors
may elicit microglial ATP release that feeds back onto neurons. P2X7 receptor activation
may lead to inflammation by activation of the “inflammasome”, a protein complex that
activates inflammatory caspases. Unique to the P2X7 receptor is that prolonged stimulation
leads to the opening of a large-conductance pore, which corresponds to a gap junction-like
hemichannel, the pannexin, panx-1, that participates in the P2X7 receptor-dependent
inflammasome activation. This recent view on P2X7 receptor-inflammasome interaction
may open unanticipated avenues for the development of novel anti-inflammatory drugs.
Francesco pointed out that we are taught during neurobiology courses that the brain
is an immunologically privileged organ; however, this does not mean that the brain
is devoid of immune cells and that immuno-mediated reactions cannot occur in the brain.
On the contrary, it is becoming increasingly clear that resident immunocompetent cells
are crucial in the physiological homeostasis of the central nervous system (CNS).
Although it was long thought that the brain was unable to mount an inflammatory response,
it is now clear that, with some relevant differences with respect to peripheral tissues,
the CNS can undergo all the typical changes of inflammation, can activate endogenous
inflammatory cells and generate inflammatory mediators. Neurons are surrounded by
a wide population of support cells (oligodendroglia, astroglia and microglia) that
establish intimate physical relationships with the neurons and exchange with them
a wealth of biochemical information. Among these cells, microglia have a special status
as these cells are both supportive and immunocompetent. In this capacity, microglia
share all the positive and negative roles of their relatives located in the periphery,
i.e. tissue macrophages. In fact, although there are no doubts that microglia have
a key protective role in CNS trauma or infections, or even during regeneration, it
is equally clear that microglia are a fundamental culprit in CNS dysfunction.
Microglia release several factors that affect neuronal functions: activated oxygen
and nitrogen species, cytokines, chemokines and growth factors. In turn, microglia
are the target of mediators released from neurons. We have only very recently started
to understand the subtleties of this exchange of information and extracellular nucleotides
have been identified among the most relevant components of this two-way traffic. Neurons
are a rich source of ATP, which has now an established role as a cotransmitter in
most major nerve types. Secretory exocytosis seems to be the most common pathway for
ATP release. Furthermore, other cells such as astrocytes may also take part in this
communication network by releasing nucleotides or neurotransmitters that in turn evoke
ATP release from neurons. IL-1β is one of the most important proinflammatory mediators,
implicated in a variety of neurodegenerative conditions. We now know that secretion
of IL-1β is the end result of a complex chain of tightly controlled intracellular
events occurring within a multimolecular structure named the “inflammasome”. Dependence
of IL-1β release on extracellular ATP makes microglia an obvious target of neuronal
activity, especially in the presence of high levels of neurotransmitter release. Under
these conditions, if microglia are also primed by exogenous or endogenous proinflammatory
factors, this may lead to sustained IL-1β release and neuronal damage. There is scattered
evidence that this mechanism may play a role in the pathogenesis of chronic CNS pathologies,
notably Alzheimer’s disease.
The afternoon session was focused on purinergic receptors in glia-neuron interactions.
An overview of ‘Purinergic receptors and signalling mechanisms’ was introduced by
Professor Geoffrey Burnstock, President of the Autonomic Neuroscience Centre, Royal
Free and University College Medical School, London, UK. He reviewed how purinergic
transmission was proposed in the early 1970s, with evidence that ATP was a neurotransmitter
in non-adrenergic, non-cholinergic nerves in the gut and urinary bladder. Later, it
was shown to be a cotransmitter with classic neurotransmitters and it is now recognised
as a cotransmitter in most, if not all, nerve types in the peripheral and central
nervous systems. Implicit in purinergic neurotransmission is the existence of postjunctional
receptors for ATP. Released ATP is broken down by ectonucleotidases to ADP, AMP and
adenosine, and in 1978 separate receptors for adenosine and AMP (named P1 receptors)
and for ATP and ADP (named P2 receptors) were proposed. In the early 1990s, P1 and
P2 receptors were cloned and characterised: four P1 receptor subtypes (A1, A2A, A2B
and A3), seven subtypes of P2X ligand-gated ion channel receptors (P2X1-7) and eight
subtypes of P2Y G protein-coupled receptors (P2Y1, 2, 4, 6, 11, 12, 13, 14). P2Y2,
4, 6 receptors are activated by the pyrimidines uridine triphosphate (UTP) or uridine
diphosphate (UDP) as well as by purine nucleotides. The cation channel is formed by
three P2X receptor subunits either forming homomultimers or heteromultimers. P2X1/2,
P2X2/3, P2X1/4, P2X1/5, P2X2/6, P2X4/6 and probably P2X4/7 heteromultimer receptors
are widely expressed in vivo and have different pharmacological properties from homomultimers.
Reverse transcription polymerase chain reaction (RT-PCR) and immunohistochemical
studies have shown widespread expression of P1 and P2 receptor mRNA and protein in
neuronal and non-neuronal tissues. Both short-term purinergic signalling in neurotransmission,
secretion and platelet aggregation and long-term (trophic) purinergic signalling in
cell proliferation, migration, differentiation and death in development and regeneration
have been recognised.
For many years it was assumed that the source of ATP was dying cells, but it is now
recognised that many cells release ATP physiologically in response to mechanical stimuli
and hypoxia, although the mechanism of ATP transport is still debated. ATP release
from nerves and some other cells is vesicular; from others it may involve ABC transporters,
connexin or pannexin hemichannels or P2X7 receptor pores. Expression of purinergic
cotransmitters and receptors shows plasticity in development and old age, in the nerves
that remain after trauma or surgery and in disease.
For many years, it was recognised that adenosine, acting through P1 (usually A1) presynaptic
receptors to inhibit the release of excitatory transmitters, was an important mechanism
in the CNS. However, in 1992, evidence was presented for ATP mediating synaptic neurotransmission
in the medial habenula and since then there has been an explosion of interest in purinergic
neurotransmission and neuromodulation in the different regions of the brain and spinal
cord. Multiple purinergic receptors have also been identified on astrocytes, oligodendrocytes
and microglia and important mechanisms involving neuron-glial cell interactions have
been recognised, as reviewed recently [1]. There is increasing interest in the role
of purinergic signalling in the pathophysiology of neurological disorders, including:
trauma, stroke and ischaemia; neurodegenerative diseases such as Alzheimer’s, Parkinson’s
and Huntington’s, multiple sclerosis and amyotrophic lateral sclerosis; migraine;
neuro-psychiatric disorders such as schizophrenia, anxiety and depression; epileptic
seizures; and neuropathic pain. Purinergic therapeutic strategies for the treatment
of these conditions are beginning to be explored.
Professor Herbert Zimmermann, from the Institute of Cell Biology and Neuroscience
Biocenter, University of Frankfurt, Germany, gave the next talk entitled ‘Regulation
of purinergic signalling by ectonucleotidases’. He described how extracellular nucleotides
are hydrolyzed by plasma membrane-located enzymes with an extracellulary oriented
catalytic site (ectonucleotidases). Ectonucleotidases modulate ligand availability
at nucleotide and nucleoside receptors. Apart from that, they serve the recycling
of nucleosides via specific cellular transport systems. Substrates of ectonucleotidases
include nucleoside triphosphates, diphosphates and monophosphates and dinucleoside
polyphosphates. The final hydrolysis products are phosphate or pyrophosphate and the
nucleoside whereby several enzyme species can be involved in completing the hydrolysis
chain. Ectonucleotidases are molecularly even more diverse than P2 receptors and include
several enzyme families. Amongst these are the ectonucleoside triphosphate diphosphohydrolase
family (E-NTPDases), the ectonucleotide pyrophosphatase/phosphodiesterase family (E-NPPases),
the alkaline phosphatases, ecto-5′-nucleotidase and a variety of enzymes involved
in the extracellular interconversion of nucleotides such as ectonucleoside diphosphokinase
and ecto-ATP:AMP phosphotransferase (adenylate kinase, myokinase). To date, most of
the ectonucleotidases have been identified and characterised in molecular and functional
terms. The enzymes are equally abundant as nucleotide receptors and reveal a wide
and partially overlapping tissue distribution.
The diversity of the individual family members is considerable and it is still difficult
to assign the modulation of purinergic signalling pathways to identified enzymes.
In the brain, members of all ectonucleotidase families are expressed. Physiological
implications include the modulation of synaptic transmission, the ATP-mediated propagation
of glial Ca2+ waves, microglial function, adult neurogenesis and the control of vascular
tone, haemostasis and thromboregulation. Research on ectonucleotidases now continues
in diverging directions, addressing e.g. structure-function relationships, overexpression
and knockdown, crystallization and atomic structure analysis and physiological analysis.
Yet, considerably more detailed information concerning tissue and cellular localisation
of the individual ectonucleotidases is required for understanding their potential
interaction with extracellular nucleotide signalling pathways. To date, NTPDase1,
NPP1, ecto-5′-nucleotidase and two isoforms of alkaline phosphatase have been deleted
in mice. As yet, no inducible knockouts are available. The development of additional
knockout models will be of great importance to further define the physiological significance
of the individual enzyme isoforms. This needs to be flanked by the development of
inhibitors that do not affect nucleotide receptors and target individual enzyme isoforms.
Together these studies will provide both an understanding of the molecular structure
and of the physiological function of ectonucleotidases at a considerably higher level
of resolution.
Professor Peter Illes, Chairman of the Department of Pharmacology, University of Leipzig,
Germany, gave the next talk entitled ‘Purinergic receptors in pain, neuroprotection
and nerve growth’. He described how noxious stimuli lead to the outflow of ATP via
the damaged cell membrane and subsequently may activate a certain subtype of ionotropic
P2X receptor (P2X3), or metabotropic P2Y receptor (P2Y1), both situated at the nociceptive
C fibre terminals. These fibres originate from sensory neurons located in nodose or
dorsal root ganglia (DRG). P2X3 receptors are algogenic by mediating depolarization,
propagated action potentials and, in consequence, glutamate release from the central
terminals of small-diameter sensory neurons in the dorsal horn of the spinal cord.
In contrast, P2Y1 receptors cause opposite effects through the blockade of voltage-sensitive
Ca2+ channels, which normally initiate transmitter release. In addition, a negative
interaction between P2Y and P2X receptors was described via G protein involvement
in the cell bodies of DRG neurons. Moreover, various nucleotides, including ATP, have
been suggested to phosphorylate, by means of ecto-protein kinases, the extracellular
loop of P2X3 receptors and thereby to increase the conductance of these receptor channels.
Eventually, long-lasting contact with subthreshold concentrations of ATP is sufficient
to induce a massive desensitization of the P2X3 receptor. Hence, P2X3 and P2Y1 receptors
alone or in concert shape the strength and duration of painful stimuli at the level
of the peripheral nervous system.
In the CNS, both neuronal damage and mechanical distortion may rapidly increase the
extracellular concentration of nucleotides. In particular, the effects of stab wound
injury and hypoxia/ischaemia have been extensively investigated. ATP can either aggravate
or ameliorate the extent and intensity of the original damage. An aggravation could
be due to the activation of P2X7 receptors, which have a low sensitivity to ATP, but
may open large holes in the plasma membrane of astrocytes, microglia, or even neurons,
initiating apoptotic or necrotic processes. All P2X receptor subtypes may lead, because
of their Ca2+ permeability, to an overload of cells by Ca2+ and thereby to apoptosis.
On the other hand, astrocytic P2Y1 receptors may mediate proliferation and the production
of glial scars interfering with the re-establishment of normal axonal connections.
In the nucleus accumbens, P2X1 and P2X7 receptors were absent on astrocytes of untreated
rats, but became expressed after mechanical damage. Similarly, P2Y2 and P2Y6 receptors
appeared only after stab wound injury on the accumbal astrocytes. Several P2 receptor
subtypes were up-regulated by the introduction of an injection cannula into the nucleus
accumbens and still more so by the application of the mixed P2X/P2Y receptor agonist
2-methylthio ATP (2-MeSATP) or the P2Y1, 12, 13 selective agonist ADP-β-S. The co-application
of selective antagonists [pyridoxal-phosphate-6-azophenyl-2′,4′-disulphonic acid (PPADS),
MRS2179] confirmed the preferential involvement of the P2Y1, 12, 13 receptors with
a minor contribution of P2X receptor subtypes. The intracerebroventricular application
of PPADS alleviated the morphological and functional consequences of ischaemia in
an in vivo stroke model (rat medial cerebral artery occlusion) confirming the pathophysiological
role of ATP.
Extracellular ATP may promote nerve growth alone or in conjunction with various growth
factors. In co-cultures of the entorhinal cortex and the hippocampus, fibre growth
was visualized by the anterograde tracer biocytin, which was placed onto the entorhinal
part of the co-culture. The entorhinal fibre outgrowth was increased by 2-MeSATP in
the absence but not in the presence of PPADS. Hence, some unidentified P2 receptors
may exert a trophic influence under these conditions. A similar effect was observed
when the ventral tegmental area/substantia nigra complex was co-cultured with the
prefrontal cortex. In conclusion, extracellular ATP, through the activation of various
P2 receptor subtypes may modulate pain, neuronal damage and nerve growth.
Professor Maria Abbracchio, Department of Pharmacological Science, University of Milan,
Italy, gave the final talk, entitled ‘Agonists and antagonists of old and new P2 receptors’.
Extracellular purine and pyrimidine nucleotides are ubiquitous signalling molecules
that modulate the function of diverse mammalian cell types and tissues under both
physiological and pathological conditions. The highly specific actions of these neurotransmitters
are mediated by the activation of two distinct families of membrane receptors: the
P2X receptor channels and the P2Y receptors belonging to the G protein-coupled seven-transmembrane
(7-TM) receptor (GPCRs) superfamily. Seven distinct P2X receptor subunits (P2X1-P2X7)
forming multimeric ligand-gated sodium and calcium channels have been identified;
conversely, eight subtypes of P2Y receptors (P2Y1,
2, 4, 6, 11, 12, 13, 14 receptors) are officially recognised by the IUPHAR (International
Union of Pharmacology) Subcommittee for P2Y Receptor Nomenclature and Classification.
Several non-selective agonists (e.g. hydrolysis-resistant adenine and uracil nucleotide
analogs) and antagonists (e.g. suramin, Reactive Blue 2, Brilliant Blue G) have been
available during the years, but it has been only recently that ligands displaying
selectivity towards specific P2 receptor subtypes have been made available. Besides
being important pharmacological tools for the characterization of the pathophysiological
roles of P2X and P2Y receptors in native systems, there is agreement that such ligands
may represent new therapeutic entities of potential interest in a variety of human
diseases, including pain, depression, stroke and chronic neurodegenerative disorders.
The design and synthesis of selective P2Y ligands has been greatly aided by the development
of three-dimensional structures of these receptors via structure-activity relationships,
mutagenesis and homology modelling studies based on the crystallization of the GPCR
rhodopsin. Detailed three-dimensional structures of P2X receptors have not been proposed
yet, due to the lack of a suitable protein template. Recent work has identified nucleotide
agonists selective for P2Y1, P2Y2 and P2Y6 receptors and nucleotide antagonists selective
for P2Y1 (MRS2179, MRS2500), P2Y12/13 (Congrelor, previously known as AR-C69931MX)
and P2X1 receptors. Selective non-nucleotide antagonists have been reported for P2Y1,
2, 6, 12, 13 and P2X2/3/P2X3 and P2X7 receptors. For example, the dinucleotide INS37217
(UP4dC) potently activates the P2Y2 receptor and the non-nucleotide antagonist A-317491
is selective for P2X2/3/P2X3 receptors.
Dr. Abbracchio described a recently reported “deorphanization” of a new P2Y receptor,
formerly known as the “orphan” GPR17 receptor. Phylogenetically and structurally,
GPR17 is closely related to both the P2Y12,
13, 14 subfamily of P2Y receptors and to CysLT1 and CysLT2 receptors. Hence, its ligand
specificity could not be predicted simply based on its phylogenetic position. It was
shown that this receptor responded dually to both uracil nucleotides and cysteinyl-leukotrienes,
a family of proinflammatory arachidonic acid metabolites. Activation of GPR17 by uracil
nucleotides can be counteracted by P2Y receptor antagonists such as MRS2179 or cangrelor,
whereas its activation by CysLTs can be blocked by already known CysLT antagonists,
such as Montelukast and Prankulast. Since both extracellular nucleotides and CysLTs
are released in great amounts in ischaemic brain, it was hypothesized that the pathological
activation of GPR17 by these endogenous ligands may contribute to ischaemia-associated
neuronal death. In line with this hypothesis, the in vivo knockdown of GPR17 by either
P2Y/CysLT antagonists or by an anti-sense oligonucleotide strategy markedly prevented
ischaemia evolution. GPR17 thus represents the first fully characterised example of
a dual GPCR responding to two distinct unrelated classes of non-peptide endogenous
ligands. However, the P2Y12 receptor has been also reported to respond to the cysteinyl-leukotriene
LTE4, suggesting that there may exist several GPCRs characterised by a dual pharmacology,
and, in particular, that the P2Y12,
13, 14 subfamily of P2Y receptors may interact with both nucleotides and CysLT with
high affinity. The existence of dual receptors opens the possibility of developing
dual ligands characterised by previously unexplored therapeutic potency. In particular,
it was envisaged that dual GPR17 antagonists may represent a novel class of potent
anti-neurodegenerative agents.
The formal presentations were followed by a discussion session with lively exchanges
of views between the speakers and members of UCB staff. Some promising therapeutic
targets were identified. Marc De Ryck thanked the speakers for their authoritative
and informative presentations and said that UCB would now consider the way forward.