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Convergence of adenosine and GABA signaling for synapse stabilization during development
Author(s) -
Ferran Gomez-Castro,
Stefania Zappettini,
Jessica C. Pressey,
Carla G. Silva,
Marion Russeau,
Nicolas Gervasi,
Marta Figueiredo,
Claire Montmasson,
Marianne Renner,
Paula M. Canas,
Francisco Q. Gonçalves,
Sofia Alçada-Morais,
Eszter Szabó,
Ricardo J. Rodrigues,
Paula Agostinho,
Ângelo R. Tomé,
Ghislaine Caillol,
Olivier Thoumine,
Xavier Nicol,
Christophe Leterrier,
Rafael Luján,
Shiva K. Tyagarajan,
Rodrigo A. Cunha,
Monique Esclapez,
Christophe Bernard,
Sabine Lévi
Publication year - 2021
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abk2055
Subject(s) - gephyrin , gabaergic , postsynaptic potential , microbiology and biotechnology , adenosine , synapse , adenylyl cyclase , chemistry , signal transduction , biology , neuroscience , receptor , biochemistry , amino acid , glycine receptor , glycine
Synapse stabilization Early in brain development, neurons connect to each other enthusiastically. With development, an overabundance of synapses is winnowed down to refine efficiently connected circuits. Inactive synapses are prime targets for elimination, whereas active synapses tend to be retained. Gomez-Castroet al . took a closer look at how those choices are made (see the Perspective by Blum and Lopes). When postsynaptic adenosine receptors are muted or do not find enough extracellular adenosine, synapses get eliminated. Neurotransmitter-dependent signaling pathways drive protein kinase A to phosphorylate the postsynaptic scaffolding molecule gephyrin. Together with a partner synaptogenic membrane protein, gephyrin is required for the stabilization of γ-aminobutyric acid receptors. Adenosine receptors thus detect synaptic activity and in turn drive the stabilization of synapses that produce such activity. —PJH

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