Nogo-A expressed in Schwann cells impairs axonal regeneration after peripheral nerve injury

J Cell Biol. 2002 Oct 14;159(1):29-35. doi: 10.1083/jcb.200206068. Epub 2002 Oct 14.

Abstract

Injured axons in mammalian peripheral nerves often regenerate successfully over long distances, in contrast to axons in the brain and spinal cord (CNS). Neurite growth-inhibitory proteins, including the recently cloned membrane protein Nogo-A, are enriched in the CNS, in particular in myelin. Nogo-A is not detectable in peripheral nerve myelin. Using regulated transgenic expression of Nogo-A in peripheral nerve Schwann cells, we show that axonal regeneration and functional recovery are impaired after a sciatic nerve crush. Nogo-A thus overrides the growth-permissive and -promoting effects of the lesioned peripheral nerve, demonstrating its in vivo potency as an inhibitor of axonal regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / physiology*
  • GAP-43 Protein / metabolism
  • Gene Expression Regulation
  • Growth Inhibitors / genetics
  • Growth Inhibitors / metabolism*
  • HeLa Cells
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Myelin Proteins / genetics
  • Myelin Proteins / metabolism*
  • Nerve Crush
  • Nerve Regeneration / physiology*
  • Nogo Proteins
  • Rats
  • Schwann Cells / metabolism*
  • Sciatic Nerve / injuries
  • Sciatic Nerve / physiology*
  • Sciatic Nerve / ultrastructure
  • Transgenes

Substances

  • GAP-43 Protein
  • Growth Inhibitors
  • Myelin Proteins
  • Nogo Proteins
  • RTN4 protein, human
  • Rtn4 protein, mouse
  • Rtn4 protein, rat