Ephexin1 is required for structural maturation and neurotransmission at the neuromuscular junction

Neuron. 2010 Jan 28;65(2):204-16. doi: 10.1016/j.neuron.2010.01.012.

Abstract

The maturation of neuromuscular junctions (NMJs) requires the topological transformation of postsynaptic acetylcholine receptor (AChR)-containing structures from a simple plaque to an elaborate structure composed of pretzel-like branches. This maturation process results in the precise apposition of the presynaptic and postsynaptic specializations. However, little is known about the molecular mechanisms underlying the plaque-to-pretzel transition of AChR clusters. In this study, we identify an essential role for the RhoGEF ephexin1 in the maturation of AChR clusters. Adult ephexin1(-/-) mice exhibit severe muscle weakness and impaired synaptic transmission at the NMJ. Intriguingly, when ephexin1 expression is deficient in vivo, the NMJ fails to mature into the pretzel-like shape, and such abnormalities can be rescued by re-expression of ephexin1. We further demonstrate that ephexin1 regulates the stability of AChR clusters in a RhoA-dependent manner. Taken together, our findings reveal an indispensible role for ephexin1 in regulating the structural maturation and neurotransmission of NMJs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Guanine Nucleotide Exchange Factors / deficiency
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / physiology*
  • Mice
  • Mice, Knockout
  • Myoblasts / physiology
  • Myoblasts / ultrastructure
  • Neuromuscular Junction / genetics
  • Neuromuscular Junction / growth & development*
  • Neuromuscular Junction / ultrastructure
  • Receptor Aggregation / physiology
  • Receptors, Cholinergic / biosynthesis
  • Receptors, Cholinergic / physiology
  • Rho Guanine Nucleotide Exchange Factors
  • Synaptic Transmission / genetics
  • Synaptic Transmission / physiology*

Substances

  • Guanine Nucleotide Exchange Factors
  • NGEF protein, human
  • Receptors, Cholinergic
  • Rho Guanine Nucleotide Exchange Factors