Building, Breaking, and Repairing Neuromuscular Synapses

Cold Spring Harb Perspect Biol. 2024 May 2;16(5):a041490. doi: 10.1101/cshperspect.a041490.

Abstract

A coordinated and complex interplay of signals between motor neurons, skeletal muscle cells, and Schwann cells controls the formation and maintenance of neuromuscular synapses. Deficits in the signaling pathway for building synapses, caused by mutations in critical genes or autoantibodies against key proteins, are responsible for several neuromuscular diseases, which cause muscle weakness and fatigue. Here, we describe the role that four key genes, Agrin, Lrp4, MuSK, and Dok7, play in this signaling pathway, how an understanding of their mechanisms of action has led to an understanding of several neuromuscular diseases, and how this knowledge has contributed to emerging therapies for treating neuromuscular diseases.

Publication types

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

MeSH terms

  • Agrin / metabolism
  • Animals
  • Humans
  • LDL-Receptor Related Proteins / metabolism
  • Motor Neurons / metabolism
  • Motor Neurons / physiology
  • Muscle Proteins / metabolism
  • Neuromuscular Diseases
  • Neuromuscular Junction*
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Receptors, Cholinergic / metabolism
  • Signal Transduction*
  • Synapses / metabolism
  • Synapses / physiology

Substances

  • Agrin
  • LDL-Receptor Related Proteins
  • Receptor Protein-Tyrosine Kinases
  • Muscle Proteins
  • LRP4 protein, human
  • Receptors, Cholinergic
  • DOK7 protein, human