Synthesis and transport of GAP-43 in entorhinal cortex neurons and perforant pathway during lesion-induced sprouting and reactive synaptogenesis

Brain Res Mol Brain Res. 1992 Jun;14(1-2):147-53. doi: 10.1016/0169-328x(92)90024-6.

Abstract

Metabolic labeling and quantitative 2D gel autoradiography were used to assess changes in the synthesis and transport of GAP-43 in entorhinal cortex (EC) neurons and perforant pathway during lesion-induced sprouting and reactive synaptogenesis. In normal adult rats, there is a high constitutive level of GAP-43 synthesis and transport in EC neurons projecting to the hippocampus. Following unilateral EC lesions, there is a 2-fold (100%) increase in the transport of newly synthesized GAP-43 to the contralateral or 'sprouting' hippocampus. The timing of this upregulation (between 6 and 15 days) suggests that changes in GAP-43 expression occur in response to the growth of presynaptic terminals during sprouting.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Axonal Transport
  • Biological Transport
  • Denervation
  • GAP-43 Protein
  • Limbic System / injuries
  • Limbic System / metabolism*
  • Male
  • Membrane Glycoproteins / metabolism*
  • Membrane Proteins*
  • Nerve Regeneration*
  • Nerve Tissue Proteins / metabolism*
  • Neuronal Plasticity*
  • Neurons / metabolism
  • Rats
  • Rats, Inbred Strains
  • Synapses / metabolism*
  • Synaptosomal-Associated Protein 25

Substances

  • GAP-43 Protein
  • Membrane Glycoproteins
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Snap25 protein, rat
  • Synaptosomal-Associated Protein 25