DCC-dependent phospholipase C signaling in netrin-1-induced neurite elongation

J Biol Chem. 2006 Feb 3;281(5):2605-11. doi: 10.1074/jbc.M512767200. Epub 2005 Nov 30.

Abstract

Netrins, a family of secreted molecules, play important roles in axon pathfinding during nervous system development. Although phosphatidylinositol signaling has been implicated in this event, how netrin-1 regulates phosphatidylinositol signaling remains poorly understood. Here we provide evidence that netrin-1 stimulates phosphatidylinositol bisphosphate hydrolysis in cortical neurons. This event appears to be mediated by DCC (deleted in colorectal cancer), but not neogenin or Unc5h2. Netrin-1 induces phospholipase Cgamma (PLCgamma) tyrosine phosphorylation. Inhibition of PLC activity attenuates netrin-1-induced cortical neurite outgrowth. These results suggest that netrin-1 regulates phosphatidylinositol turnover and demonstrate a crucial role of PLC signaling in netrin-1-induced neurite elongation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • DCC Receptor
  • Humans
  • Mice
  • Nerve Growth Factors / physiology*
  • Netrin-1
  • Neurites / physiology*
  • Neurons / cytology
  • Phosphatidylinositol Phosphates / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Cell Surface / physiology*
  • Signal Transduction*
  • Tumor Suppressor Proteins / physiology*
  • Type C Phospholipases / physiology*

Substances

  • DCC Receptor
  • DCC protein, human
  • NTN1 protein, human
  • Nerve Growth Factors
  • Ntn1 protein, mouse
  • Ntn1 protein, rat
  • Phosphatidylinositol Phosphates
  • Receptors, Cell Surface
  • Tumor Suppressor Proteins
  • Netrin-1
  • Type C Phospholipases