Disruption of the gene for the myelin-associated glycoprotein improves axonal regrowth along myelin in C57BL/Wlds mice

Neuron. 1996 Jun;16(6):1107-13. doi: 10.1016/s0896-6273(00)80137-3.

Abstract

The myelin-associated glycoprotein (MAG) has been shown to be inhibitory for certain neurons in vitro (Mukhopadhyay et al., 1994; McKerracher et al., 1994). To investigate whether MAG is an inhibitory component in peripheral myelin in vivo, MAG-deficient mutant mice were cross-bred with C57BL/Wlds mice that have delayed lesion-induced myelin degeneration and axon regrowth. While in crushed nerves of C57BL/Wlds mice expressing MAG, only 16% of myelin sheaths were associated with regrowing axons, this number was doubled in MAG-deficient C57BL/Wlds mice. These observations suggest that the absence of MAG may contribute to the improved axonal regrowth in the double mutants. Therefore, degeneration of MAG-containing myelin might be an important prerequisite to optimize axonal regrowth after peripheral nerve injury.

MeSH terms

  • Animals
  • Axons / physiology*
  • Axons / ultrastructure
  • Genes / genetics*
  • Immunohistochemistry
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Electron
  • Myelin-Associated Glycoprotein / genetics*

Substances

  • Myelin-Associated Glycoprotein