Biological activity of neurotrophins is dependent on recruitment of Rac1 to lipid rafts

Biochem Biophys Res Commun. 2005 Feb 4;327(1):150-4. doi: 10.1016/j.bbrc.2004.11.151.

Abstract

The Rho family of small GTPases, key regulators of the actin cytoskeleton in eukaryotic cells, is implicated in the control of neuronal morphology. Here, we report that neurotrophin dependent cytoskeletal changes, characteristic of the phenotype of Rac1, in the hippocampal neurons or PC12 cells are inhibited by the disruption of lipid raft integrity. Activation of Rac1 induced by NGF is impaired in cholesterol-depleted PC12 cells. Pretreatment with gammaGTP shifted significant amount of Rac1, presumably in a GTP-bound form, from non-raft to raft fractions. Proper recruitment of activated Rac1 to lipid rafts, structures that represent specialized signaling organelles, is of fundamental importance in determining neurotrophins' bioactivity.

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / pharmacology*
  • Cells, Cultured
  • Cholesterol / metabolism
  • Guanosine Triphosphate / metabolism
  • Guanosine Triphosphate / pharmacology
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Membrane Microdomains / chemistry*
  • Membrane Microdomains / metabolism*
  • Nerve Growth Factor / pharmacology*
  • PC12 Cells
  • Rats
  • rac1 GTP-Binding Protein / metabolism*

Substances

  • Brain-Derived Neurotrophic Factor
  • Guanosine Triphosphate
  • Nerve Growth Factor
  • Cholesterol
  • rac1 GTP-Binding Protein