ERK1/2-mediated Schwann cell proliferation in the regenerating sciatic nerve by treadmill training

J Neurotrauma. 2009 Oct;26(10):1733-44. doi: 10.1089/neu.2008.0711.

Abstract

Proliferation of Schwann cells in the injured peripheral nerve supports axonal regeneration, and physical training in experimental animals has been shown to promote nerve regeneration. Extracellular signal-regulated kinase 1/2 (ERK1/2) activity can mediate neuronal responses to lesion signals, but its role in non-neuronal cells in the injured area is largely unknown. Here we report that treadmill training (TMT) facilitates axonal regeneration via the upregulation of phospho-ERK1/2 protein levels in Schwann cells in the injured sciatic nerve. Low-intensity, but not high-intensity, TMT increased neurite outgrowth of dorsal root ganglion (DRG) sensory neurons and potentiated Schwann cell proliferation. TMT elevated levels of GAP-43 mRNA and protein, and phospho-ERK1/2 protein in the injured sciatic nerves. TMT also enhanced phospho-c-Jun protein levels in the injured nerve. In-vivo administration of the ERK1/2 inhibitor PD98059 eliminated phospho-c-Jun, suggesting ERK1/2 phosphorylation of the c-Jun protein. PD98059 treatment decreased levels of BrdU-labeled proliferating Schwann cells in the distal portion of the injured nerve, and delayed the axonal regrowth that was promoted by TMT. The present data suggest that increased ERK1/2 activity in Schwann cells may play an important role in TMT-mediated enhancement of axonal regeneration in the injured peripheral nerve.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation
  • Denervation
  • Disease Models, Animal
  • Enzyme Activation / physiology
  • Enzyme Inhibitors / pharmacology
  • Exercise Test
  • Exercise Therapy / methods*
  • GAP-43 Protein / genetics
  • GAP-43 Protein / metabolism
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / metabolism
  • Growth Cones / metabolism
  • Growth Cones / ultrastructure
  • Male
  • Mitogen-Activated Protein Kinase 3 / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 3 / metabolism*
  • Nerve Regeneration / physiology*
  • Neurites / metabolism
  • Neurites / ultrastructure
  • Physical Conditioning, Animal / physiology
  • Proto-Oncogene Proteins c-jun / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Schwann Cells / cytology
  • Schwann Cells / enzymology*
  • Sciatic Nerve / cytology
  • Sciatic Nerve / injuries
  • Sciatic Nerve / metabolism
  • Sciatic Neuropathy / enzymology*
  • Sciatic Neuropathy / physiopathology
  • Sciatic Neuropathy / rehabilitation*
  • Up-Regulation / physiology

Substances

  • Enzyme Inhibitors
  • GAP-43 Protein
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • Mitogen-Activated Protein Kinase 3