The HSPG syndecan is a core organizer of cholinergic synapses

Author:

Zhou Xin1ORCID,Vachon Camille1,Cizeron Mélissa1ORCID,Romatif Océane1,Bülow Hannes E.2,Jospin Maëlle1,Bessereau Jean-Louis1ORCID

Affiliation:

1. Université de Lyon, Université Claude Bernard Lyon 1, Centre National de la Recherche Scientifique Unite Mixte de Recherche 5310, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Lyon, France

2. Department of Genetics and Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY

Abstract

The extracellular matrix has emerged as an active component of chemical synapses regulating synaptic formation, maintenance, and homeostasis. The heparan sulfate proteoglycan (HSPG) syndecans are known to regulate cellular and axonal migration in the brain. They are also enriched at synapses, but their synaptic functions remain more elusive. Here, we show that SDN-1, the sole orthologue of syndecan in C. elegans, is absolutely required for the synaptic clustering of homomeric α7-like acetylcholine receptors (AChRs) and regulates the synaptic content of heteromeric AChRs. SDN-1 is concentrated at neuromuscular junctions (NMJs) by the neurally secreted synaptic organizer Ce-Punctin/MADD-4, which also activates the transmembrane netrin receptor DCC. Those cooperatively recruit the FARP and CASK orthologues that localize α7-like-AChRs at cholinergic NMJs through physical interactions. Therefore, SDN-1 stands at the core of the cholinergic synapse organization by bridging the extracellular synaptic determinants to the intracellular synaptic scaffold that controls the postsynaptic receptor content.

Funder

National Institutes of Health

European Research Council

Université de Lyon

French National Research Agency

Publisher

Rockefeller University Press

Subject

Cell Biology

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