A midline switch of receptor processing regulates commissural axon guidance in vertebrates

Genes Dev. 2010 Feb 15;24(4):396-410. doi: 10.1101/gad.542510.

Abstract

Commissural axon guidance requires complex modulations of growth cone sensitivity to midline-derived cues, but underlying mechanisms in vertebrates remain largely unknown. By using combinations of ex vivo and in vivo approaches, we uncovered a molecular pathway controlling the gain of response to a midline repellent, Semaphorin3B (Sema3B). First, we provide evidence that Semaphorin3B/Plexin-A1 signaling participates in the guidance of commissural projections at the vertebrate ventral midline. Second, we show that, at the precrossing stage, commissural neurons synthesize the Neuropilin-2 and Plexin-A1 Semaphorin3B receptor subunits, but Plexin-A1 expression is prevented by a calpain1-mediated processing, resulting in silencing commissural responsiveness. Third, we report that, during floor plate (FP) in-growth, calpain1 activity is suppressed by local signals, allowing Plexin-A1 accumulation in the growth cone and sensitization to Sema3B. Finally, we show that the FP cue NrCAM mediates the switch of Plexin-A1 processing underlying growth cone sensitization to Sema3B. This reveals pathway-dependent modulation of guidance receptor processing as a novel mechanism for regulating guidance decisions at intermediate targets.

Publication types

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

MeSH terms

  • Animals
  • Axons / metabolism
  • Axons / physiology*
  • Calpain / metabolism
  • Cell Adhesion Molecules / metabolism
  • Chick Embryo
  • Embryo, Mammalian
  • Gene Expression Regulation, Developmental
  • Mice
  • Nerve Tissue Proteins / metabolism
  • Neurons / cytology*
  • Neurons / metabolism
  • Neuropilin-2 / metabolism
  • Semaphorins / metabolism
  • Signal Transduction*

Substances

  • Cell Adhesion Molecules
  • Nerve Tissue Proteins
  • Neuropilin-2
  • Semaphorins
  • plexin
  • Calpain