The specific α-neurexin interactor calsyntenin-3 promotes excitatory and inhibitory synapse development

Neuron. 2013 Oct 2;80(1):113-28. doi: 10.1016/j.neuron.2013.07.016. Epub 2013 Oct 2.

Abstract

Perturbations of cell surface synapse-organizing proteins, particularly α-neurexins, contribute to neurodevelopmental and psychiatric disorders. From an unbiased screen, we identify calsyntenin-3 (alcadein-β) as a synapse-organizing protein unique in binding and recruiting α-neurexins, but not β-neurexins. Calsyntenin-3 is present in many pyramidal neurons throughout cortex and hippocampus but is most highly expressed in interneurons. The transmembrane form of calsyntenin-3 can trigger excitatory and inhibitory presynapse differentiation in contacting axons. However, calsyntenin-3-shed ectodomain, which represents about half the calsyntenin-3 pool in brain, suppresses the ability of multiple α-neurexin partners including neuroligin 2 and LRRTM2 to induce presynapse differentiation. Clstn3⁻/⁻ mice show reductions in excitatory and inhibitory synapse density by confocal and electron microscopy and corresponding deficits in synaptic transmission. These results identify calsyntenin-3 as an α-neurexin-specific binding partner required for normal functional GABAergic and glutamatergic synapse development.

Publication types

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

MeSH terms

  • Animals
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / metabolism*
  • Cell Adhesion Molecules, Neuronal / metabolism
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Cerebral Cortex / growth & development
  • Cerebral Cortex / pathology
  • Hippocampus / cytology*
  • Hippocampus / growth & development
  • Hippocampus / metabolism
  • Hippocampus / ultrastructure
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Nerve Tissue Proteins / metabolism
  • Neural Cell Adhesion Molecules / metabolism
  • Neurons / cytology
  • Neurons / metabolism*
  • Rats
  • Receptors, Cell Surface / metabolism
  • Synapses / genetics
  • Synapses / metabolism*
  • Synaptic Transmission / physiology*

Substances

  • CLSTN3 protein, rat
  • Calcium-Binding Proteins
  • Cell Adhesion Molecules, Neuronal
  • LRRTM2 protein, rat
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Neural Cell Adhesion Molecules
  • Nrxn1 protein, rat
  • Receptors, Cell Surface
  • neuroligin 2