The role of Kalirin9 in p75/nogo receptor-mediated RhoA activation in cerebellar granule neurons

J Biol Chem. 2008 Sep 5;283(36):24690-7. doi: 10.1074/jbc.M802188200. Epub 2008 Jul 14.

Abstract

p75 and the Nogo receptor form a signaling unit for myelin inhibitory molecules, with p75 being responsible for RhoA activation. Because p75 lacks the GDP/GTP exchange factor domain, it has remained unclear how p75 activates RhoA. Here, we report that Kalirin9, a dual RhoGEF, binds p75 directly and regulates p75-Nogo receptor-dependent RhoA activation and neurite inhibition in response to myelin-associated glycoprotein. The region of p75 that Kalirin9 binds includes its mastoparan-like fifth helix, which was shown to recruit RhoGDI-RhoA. As predicted from the presence of a shared binding site, we found that Kalirin9 competes with RhoGDI for p75 binding in a dose-dependent manner in vitro. In line with these data, myelin-associated glycoprotein addition to cerebellar granule neurons resulted in a reduction in the association of Kalirin9 with p75, and a simultaneous increase in the binding of RhoGDI to p75. These results reveal a mechanism by which the fifth helix of p75 regulates RhoA activation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cerebellum / cytology
  • Cerebellum / metabolism*
  • GPI-Linked Proteins
  • Guanine Nucleotide Dissociation Inhibitors / metabolism
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Myelin Proteins
  • Myelin-Associated Glycoprotein / metabolism
  • Nerve Tissue Proteins
  • Neurites / metabolism*
  • Nogo Receptor 1
  • Protein Structure, Secondary / physiology
  • Protein Structure, Tertiary / physiology
  • Rats
  • Receptors, Cell Surface
  • Receptors, Growth Factor
  • Receptors, Nerve Growth Factor / metabolism*
  • Receptors, Peptide / metabolism*
  • Rho Guanine Nucleotide Exchange Factors
  • rho-Specific Guanine Nucleotide Dissociation Inhibitors
  • rhoA GTP-Binding Protein / metabolism*

Substances

  • GPI-Linked Proteins
  • Guanine Nucleotide Dissociation Inhibitors
  • Guanine Nucleotide Exchange Factors
  • Kalrn protein, rat
  • Myelin Proteins
  • Myelin-Associated Glycoprotein
  • Nerve Tissue Proteins
  • Nogo Receptor 1
  • Receptors, Cell Surface
  • Receptors, Growth Factor
  • Receptors, Nerve Growth Factor
  • Receptors, Peptide
  • Rho Guanine Nucleotide Exchange Factors
  • Rtn4r protein, rat
  • rho-Specific Guanine Nucleotide Dissociation Inhibitors
  • Ngfr protein, rat
  • rhoA GTP-Binding Protein