A new millenium for spinal cord regeneration: growth-associated genes

Spine (Phila Pa 1976). 2002 Sep 1;27(17):1946-9. doi: 10.1097/00007632-200209010-00030.

Abstract

Introduction: Neurons surviving spinal cord injury undergo extensive reorganization that may result in the formation of functional synaptic contacts. Many neurons, however, fail to activate the necessary mechanisms for successful regeneration. In this review, we discuss the implications of growth cone genes that we have correlated with successful spinal cord axonal regeneration.

Method: Factors that inhibit regeneration, and activation of genes that promote it are discussed.

Results/discussion: The early progress n understanding mechanisms that seem to promote or inhibit regeneration in the central nervous system may have significant clinical utility in the future.

Publication types

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

MeSH terms

  • Animals
  • Calmodulin-Binding Proteins*
  • Cytoskeletal Proteins / genetics
  • GAP-43 Protein / genetics
  • Growth Cones / physiology
  • Humans
  • Mice
  • Mice, Transgenic
  • Myelin Proteins / genetics
  • Nerve Growth Factors / genetics*
  • Nerve Regeneration / genetics*
  • Nerve Tissue Proteins*
  • Neurons / physiology
  • Nogo Proteins
  • Spinal Cord Diseases / genetics*
  • Spinal Cord Diseases / therapy

Substances

  • Basp1 protein, mouse
  • Calmodulin-Binding Proteins
  • Cytoskeletal Proteins
  • GAP-43 Protein
  • Myelin Proteins
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Nogo Proteins
  • RTN4 protein, human
  • Rtn4 protein, mouse