The HSPG syndecan is a core organizer of cholinergic synapses

J Cell Biol. 2021 Sep 6;220(9):e202011144. doi: 10.1083/jcb.202011144. Epub 2021 Jul 2.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / metabolism
  • Angiopoietin-Like Protein 4 / genetics
  • Angiopoietin-Like Protein 4 / metabolism
  • Animals
  • Brain / cytology
  • Brain / metabolism
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / metabolism
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • DCC Receptor / genetics
  • DCC Receptor / metabolism
  • Extracellular Matrix / chemistry
  • Extracellular Matrix / metabolism
  • Gene Expression Regulation
  • Guanylate Kinases / genetics
  • Guanylate Kinases / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Neuromuscular Junction / metabolism*
  • Neuromuscular Junction / ultrastructure
  • Neurons / cytology
  • Neurons / metabolism
  • Receptors, Cholinergic / genetics
  • Receptors, Cholinergic / metabolism*
  • Synapses / metabolism*
  • Synapses / ultrastructure
  • Synaptic Transmission / genetics
  • Syndecans / genetics
  • Syndecans / metabolism*

Substances

  • Angiopoietin-Like Protein 4
  • Caenorhabditis elegans Proteins
  • DCC Receptor
  • MADD-4 protein, C elegans
  • Nerve Tissue Proteins
  • Receptors, Cholinergic
  • Syndecans
  • Guanylate Kinases
  • Acetylcholine