Neurite outgrowth from PC12 cells is enhanced by an inhibitor of mechanical channels

Neurosci Lett. 2010 Sep 6;481(2):115-9. doi: 10.1016/j.neulet.2010.06.066. Epub 2010 Jun 26.

Abstract

GsMTx4, a peptide inhibitor for mechanosensitive ion channels (MSCs), promoted neurite outgrowth from PC12 cells in the presence of NGF in a dose-dependent manner between 5 and 100 microM peptide. Enhanced neurite growth required >12 h of peptide exposure in cells grown with NGF. Adsorption of GsMTx4 to serum proteins in the media lowered the free peptide concentration of 100 microM to a free concentration of 5 microM, a concentration shown to completely inhibit MSCs in the patch clamp assay. Outside-out patches from PC12 cells grown in NGF had mechanically activated cation channels that were reversibly inhibited by GsMTx4. These results are similar to those observed by Gomez and co-workers in Xenopus spinal cord. The inhibition of mechanosensitive channels by GsMTx4 may be a useful approach to accelerate regeneration of neurons in neurodegenerative diseases and spinal cord injury.

MeSH terms

  • Analysis of Variance
  • Animals
  • Chromatography, High Pressure Liquid / methods
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Intercellular Signaling Peptides and Proteins
  • Ion Channels / antagonists & inhibitors*
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Nerve Growth Factor / pharmacology
  • Neurites / drug effects*
  • PC12 Cells / cytology
  • PC12 Cells / drug effects
  • Patch-Clamp Techniques / methods
  • Peptides / pharmacology*
  • Physical Stimulation / methods
  • Rats
  • Spider Venoms / pharmacology*
  • Time Factors

Substances

  • Intercellular Signaling Peptides and Proteins
  • Ion Channels
  • MTx4 protein, Grammostola spatulata
  • Peptides
  • Spider Venoms
  • Nerve Growth Factor