NGL-3-induced presynaptic differentiation of hippocampal neurons in an afadin-dependent, nectin-1-independent manner

Genes Cells. 2017 Aug;22(8):742-755. doi: 10.1111/gtc.12510. Epub 2017 Jul 11.

Abstract

A hippocampal mossy fiber synapse, which is implicated in learning and memory, has a complex structure. We have previously shown using afadin-deficient mice that afadin plays multiple roles in the structural and functional differentiations of this synapse. We investigated here using a co-culture system with cultured hippocampal neurons and non-neuronal COS-7 cells expressing synaptogenic cell adhesion molecules (CAMs) whether afadin is involved in the presynaptic differentiation of hippocampal synapses. Postsynaptic CAMs NGL-3 (alias, a Lrrc4b gene product) and neuroligin induced presynaptic differentiation by trans-interacting with their respective presynaptic binding CAMs LAR (alias, a Ptprf gene product) and neurexin. This activity of NGL-3, but not neuroligin, was dependent on afadin, but not the afadin-binding presynaptic CAM nectin-1. The afadin-binding postsynaptic CAM nectin-3 did not induce presynaptic differentiation. Immunofluorescence and immunoelectron microscopy analyses showed that afadin was localized mainly at puncta adherentia junctions, but partly at synaptic junctions, of the mossy fiber synapse. β-Catenin and γ-catenin known to bind to LAR were co-immunoprecipitated with afadin from the lysate of mouse brain. These results suggest that afadin is involved in the NGL-3-LAR system-induced presynaptic differentiation of hippocampal neurons cooperatively with β-catenin and γ-catenin in a nectin-1-independent manner.

MeSH terms

  • Animals
  • COS Cells
  • Cells, Cultured
  • Chlorocebus aethiops
  • GPI-Linked Proteins / genetics
  • GPI-Linked Proteins / metabolism*
  • Hippocampus / cytology
  • Hippocampus / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism*
  • Mossy Fibers, Hippocampal / metabolism*
  • Mossy Fibers, Hippocampal / ultrastructure
  • Nectins / genetics
  • Nectins / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Neurogenesis*
  • Neurons / cytology
  • Neurons / metabolism*
  • Protein Binding
  • beta Catenin / metabolism
  • gamma Catenin / metabolism

Substances

  • GPI-Linked Proteins
  • Microfilament Proteins
  • NGL3 protein, mouse
  • Nectins
  • Nerve Tissue Proteins
  • afadin
  • beta Catenin
  • gamma Catenin