Rho GTPases regulate distinct aspects of dendritic arbor growth in Xenopus central neurons in vivo

Nat Neurosci. 2000 Mar;3(3):217-25. doi: 10.1038/72920.

Abstract

The development and structural plasticity of dendritic arbors are governed by several factors, including synaptic activity, neurotrophins and other growth-regulating molecules. The signal transduction pathways leading to dendritic structural changes are unknown, but likely include cytoskeleton regulatory components. To test whether GTPases regulate dendritic arbor development, we collected time-lapse images of single optic tectal neurons in albino Xenopus tadpoles expressing dominant negative or constitutively active forms of Rac, Cdc42 or RhoA. Analysis of images collected at two-hour intervals over eight hours indicated that enhanced Rac activity selectively increased branch additions and retractions, as did Cdc42 to a lesser extent. Activation of endogenous RhoA decreased branch extension without affecting branch additions and retractions, whereas dominant-negative RhoA increased branch extension. Finally, we provide data suggesting that RhoA mediates the promotion of normal dendritic arbor development by NMDA receptor activation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 2-Amino-5-phosphonovalerate / pharmacology
  • Actins / metabolism
  • Animals
  • Cell Size / drug effects
  • Cytoskeleton / drug effects
  • Cytoskeleton / metabolism
  • Dendrites / drug effects
  • Dendrites / enzymology*
  • Dendrites / physiology*
  • Dendrites / ultrastructure
  • Enzyme Activation / genetics
  • Genes, Dominant / genetics
  • Humans
  • Larva / cytology
  • Larva / drug effects
  • Mutation / genetics
  • Neuronal Plasticity / drug effects
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Receptors, N-Methyl-D-Aspartate / physiology
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction / drug effects
  • Superior Colliculi / cytology*
  • Superior Colliculi / drug effects
  • Superior Colliculi / enzymology
  • Superior Colliculi / metabolism
  • Vaccinia virus / genetics
  • Xenopus laevis
  • cdc42 GTP-Binding Protein / genetics
  • cdc42 GTP-Binding Protein / metabolism
  • rac GTP-Binding Proteins / genetics
  • rac GTP-Binding Proteins / metabolism
  • rho GTP-Binding Proteins / genetics
  • rho GTP-Binding Proteins / metabolism*
  • rhoA GTP-Binding Protein / genetics
  • rhoA GTP-Binding Protein / metabolism

Substances

  • Actins
  • Receptors, N-Methyl-D-Aspartate
  • Recombinant Fusion Proteins
  • 2-Amino-5-phosphonovalerate
  • cdc42 GTP-Binding Protein
  • rac GTP-Binding Proteins
  • rho GTP-Binding Proteins
  • rhoA GTP-Binding Protein