GAP43 stimulates inositol trisphosphate-mediated calcium release in response to hypotonicity

EMBO J. 2003 Jun 16;22(12):3004-14. doi: 10.1093/emboj/cdg294.

Abstract

The identification of osmo/mechanosensory proteins in mammalian sensory neurons is still elusive. We have used an expression cloning approach to screen a human dorsal root ganglion cDNA library to look for proteins that respond to hypotonicity by raising the intracellular Ca(2+) concentration ([Ca(2+)](i)). We report the unexpected identification of GAP43 (also known as neuromodulin or B50), a membrane-anchored neuronal protein implicated in axonal growth and synaptic plasticity, as an osmosensory protein that augments [Ca(2+)](i) in response to hypotonicity. Palmitoylation of GAP43 plays an important role in the protein osmosensitivity. Depletion of intracellular stores or inhibition of phospholipase C (PLC) activity abrogates hypotonicity-evoked, GAP43-mediated [Ca(2+)](i) elevations. Notably, hypotonicity promoted the selective association of GAP43 with the PLC-delta(1) isoform, and a concomitant increase in inositol-1,4,5-trisphosphate (IP(3)) formation. Collectively, these findings indicate that hypo-osmotic activation of GAP43 induces Ca(2+) release from IP(3)-sensitive intracellular stores. The osmosensitivity of GAP43 furnishes a mechanistic framework that links axon elongation with phospho inositide metabolism, spontaneous triggering of cytosolic Ca(2+) transients and the regulation of actin dynamics and motility at the growth cone in response to temporal and local mechanical forces.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Calcium / metabolism*
  • Cell Line
  • Cell Size
  • Cytoskeleton / metabolism
  • Enzyme Activation
  • Fluorescent Dyes / metabolism
  • Fura-2 / analogs & derivatives*
  • Fura-2 / metabolism
  • GAP-43 Protein / metabolism*
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / physiology
  • Humans
  • Hypotonic Solutions
  • Inositol 1,4,5-Trisphosphate / metabolism*
  • Isoenzymes / antagonists & inhibitors
  • Isoenzymes / metabolism
  • Mechanotransduction, Cellular
  • Membrane Microdomains / metabolism
  • Osmolar Concentration
  • Phospholipase C delta
  • Protein Kinase C / metabolism
  • Sensory Receptor Cells / metabolism
  • Signal Transduction*
  • Type C Phospholipases / antagonists & inhibitors
  • Type C Phospholipases / metabolism
  • Water-Electrolyte Balance / physiology*

Substances

  • Actins
  • Fluorescent Dyes
  • GAP-43 Protein
  • Hypotonic Solutions
  • Isoenzymes
  • fura-2-am
  • Inositol 1,4,5-Trisphosphate
  • Protein Kinase C
  • Type C Phospholipases
  • Phospholipase C delta
  • Calcium
  • Fura-2