Convergence of adenosine and GABA signaling for synapse stabilization during development

Author:

Gomez-Castro Ferran1ORCID,Zappettini Stefania2ORCID,Pressey Jessica C.13ORCID,Silva Carla G.24,Russeau Marion1,Gervasi Nicolas15ORCID,Figueiredo Marta6ORCID,Montmasson Claire1ORCID,Renner Marianne1ORCID,Canas Paula M.4ORCID,Gonçalves Francisco Q.4ORCID,Alçada-Morais Sofia4ORCID,Szabó Eszter4ORCID,Rodrigues Ricardo J.4ORCID,Agostinho Paula47ORCID,Tomé Angelo R.48ORCID,Caillol Ghislaine9,Thoumine Olivier10,Nicol Xavier11ORCID,Leterrier Christophe9ORCID,Lujan Rafael12ORCID,Tyagarajan Shiva K.6ORCID,Cunha Rodrigo A.47ORCID,Esclapez Monique2,Bernard Christophe2ORCID,Lévi Sabine1ORCID

Affiliation:

1. INSERM UMR-S 1270, Sorbonne Université, Institut du Fer à Moulin, Paris, France.

2. Aix Marseille Université, INSERM, INS, Institut de Neurosciences des Systèmes, Marseille, France.

3. Department of Cell and Systems Biology, University of Toronto, Toronto, ON M5S 3G5, Canada.

4. CNC-Center for Neuroscience and Cell Biology, University of Coimbra, 3004-504 Coimbra, Portugal.

5. Center for Interdisciplinary Research in Biology, College de France, INSERM U1050, CNRS UMR7241, Labex Memolife, Paris, France.

6. Institute of Pharmacology and Toxicology, University of Zürich, 8057 Zürich, Switzerland.

7. Faculty of Medicine, University of Coimbra, 3004-504 Coimbra, Portugal.

8. Department of Life Sciences, University of Coimbra, 3000-456 Coimbra, Portugal.

9. Aix Marseille Université, CNRS, INP UMR7051, NeuroCyto, Marseille, France.

10. Université Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience, IINS, UMR 5297, Bordeaux, France.

11. Sorbonne Université, Inserm, CNRS, Institut de la Vision, Paris, France.

12. Synaptic Structure Laboratory, Instituto de Investigación en Discapacidades Neurológicas (IDINE), Departamento Ciencias Médicas, Facultad de Medicina, Universidad Castilla-La Mancha, Campus Biosanitario, 02008 Albacete, Spain.

Abstract

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-Castro et 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

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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