SIP30 is regulated by ERK in peripheral nerve injury-induced neuropathic pain

J Biol Chem. 2009 Oct 30;284(44):30138-47. doi: 10.1074/jbc.M109.036756. Epub 2009 Sep 1.

Abstract

ERK plays an important role in chronic neuropathic pain. However, the underlying mechanism is largely unknown. Here we show that in chronic constriction injury-treated rat spinal cords, up-regulation of SIP30 (SNAP25-interacting protein 30), which is involved in the development and maintenance of chronic constriction injury-induced neuropathic pain, correlates with ERK activation and that the up-regulation of SIP30 is suppressed by intrathecal delivery of the MEK inhibitor U0126. In PC12 cells, up-regulation of SIP30 by nerve growth factor is also dependent on ERK activation. We found that there is an ERK-responsive region in the rat sip30 promoter. Activation of ERK promotes the recruitment of the transcription factor cyclic AMP-response element-binding protein to the sip30 gene promoter. Taken together, our results provide a potential downstream target of ERK activation-mediated neuropathic pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosomal Proteins, Non-Histone / genetics*
  • Cyclic AMP / genetics
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Extracellular Signal-Regulated MAP Kinases / physiology
  • Nerve Tissue Proteins / genetics*
  • Neuralgia / etiology
  • Neuralgia / metabolism*
  • PC12 Cells
  • Peripheral Nerve Injuries*
  • Rats
  • Response Elements
  • Spinal Cord
  • Transcription Factors
  • Up-Regulation

Substances

  • Chromosomal Proteins, Non-Histone
  • Nerve Tissue Proteins
  • Transcription Factors
  • Zwint protein, rat
  • Cyclic AMP
  • Extracellular Signal-Regulated MAP Kinases