TrkB-mediated activation of geranylgeranyltransferase I promotes dendritic morphogenesis

Proc Natl Acad Sci U S A. 2008 Nov 4;105(44):17181-6. doi: 10.1073/pnas.0800846105. Epub 2008 Oct 28.

Abstract

Dendrite morphogenesis is regulated by neuronal activity or neurotrophins, which may function by activating intrinsic signaling proteins, including Rho family GTPases. Here we report that activity- and brain-derived neurotrophic factor (BDNF)-dependent dendritic morphogenesis requires activation of geranylgeranyltransferase I (GGT), a prenyltransferase that mediates lipid modification of Rho GTPases. Dendritic arborization in cultured hippocampal neurons was promoted by over-expression of GGT, and reduced by inhibition or down-regulation of GGT. Furthermore, GGT was activated by neuronal depolarization or BDNF, both of which promote dendritic arborization, in cultured hippocampal neurons. Moreover, exploration of a novel environment caused activation of GGT in the mice hippocampus, suggesting that neural activity activates GGT in vivo. Interestingly, GGT was physically associated with tropomyosin-related kinase B (TrkB), the receptor for BDNF, and this association was enhanced by depolarization. Disrupting the GGT-TrkB interaction or down-regulating GGT activity attenuated depolarization- or BDNF-induced dendrite development. Finally, the GGT effect on dendrite arborization was prevented by over-expressing Rac1 with the prenylation site deleted or mutated. Thus depolarization- or BDNF-dependent dendrite development may be mediated by GGT-induced prenylation of Rho GTPases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkyl and Aryl Transferases / genetics
  • Alkyl and Aryl Transferases / metabolism*
  • Animals
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cells, Cultured
  • Dendrites / enzymology*
  • Dendrites / ultrastructure*
  • Humans
  • Mice
  • Mice, Inbred ICR
  • Morphogenesis / physiology*
  • Neurons / metabolism
  • Prenylation
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, trkB / metabolism*
  • Transfection
  • rac1 GTP-Binding Protein / metabolism

Substances

  • Brain-Derived Neurotrophic Factor
  • Alkyl and Aryl Transferases
  • geranylgeranyltransferase type-I
  • Receptor, trkB
  • rac1 GTP-Binding Protein