XTRPC1-dependent chemotropic guidance of neuronal growth cones

Nat Neurosci. 2005 Jun;8(6):730-5. doi: 10.1038/nn1459. Epub 2005 May 8.

Abstract

Calcium arising through release from intracellular stores and from influx across the plasma membrane is essential for signalling by specific guidance cues and by factors that inhibit axon regeneration. The mediators of calcium influx in these cases are largely unknown. Transient receptor potential channels (TRPCs) belong to a superfamily of Ca2+-permeable, receptor-operated channels that have important roles in sensing and responding to changes in the local environment. Here we report that XTRPC1, a Xenopus homolog of mammalian TRPC1, is required for proper growth cone turning responses of Xenopus spinal neurons to microscopic gradients of netrin-1, brain-derived neurotrophic factor and myelin-associated glycoprotein, but not to semaphorin 3A. Furthermore, XTRPC1 is required for midline guidance of axons of commissural interneurons in the developing Xenopus spinal cord. Thus, members of the TRPC family may serve as a key mediator for the Ca2+ influx that regulates axon guidance during development and inhibits axon regeneration in adulthood.

Publication types

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

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / metabolism
  • Brain-Derived Neurotrophic Factor / pharmacology
  • Calcium Channels / drug effects
  • Calcium Channels / metabolism*
  • Calcium Signaling / drug effects
  • Calcium Signaling / physiology*
  • Cell Communication / physiology
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Movement / drug effects
  • Cell Movement / physiology
  • Chemotaxis / drug effects
  • Chemotaxis / physiology*
  • Cues
  • Embryo, Nonmammalian
  • Functional Laterality / physiology
  • Growth Cones / drug effects
  • Growth Cones / metabolism*
  • Growth Cones / ultrastructure
  • Growth Inhibitors / metabolism
  • Interneurons / cytology
  • Interneurons / metabolism
  • Myelin-Associated Glycoprotein / metabolism
  • Myelin-Associated Glycoprotein / pharmacology
  • Nerve Growth Factors / metabolism
  • Nerve Growth Factors / pharmacology
  • Nerve Regeneration / drug effects
  • Nerve Regeneration / physiology
  • Nervous System / cytology
  • Nervous System / embryology*
  • Nervous System / metabolism
  • Netrin-1
  • Spinal Cord / cytology
  • Spinal Cord / embryology
  • Spinal Cord / metabolism
  • TRPC Cation Channels
  • Tumor Suppressor Proteins / metabolism
  • Tumor Suppressor Proteins / pharmacology
  • Xenopus Proteins / drug effects
  • Xenopus Proteins / metabolism*
  • Xenopus laevis

Substances

  • Brain-Derived Neurotrophic Factor
  • Calcium Channels
  • Growth Inhibitors
  • Myelin-Associated Glycoprotein
  • Nerve Growth Factors
  • TRPC Cation Channels
  • TRPC1 protein, Xenopus
  • Tumor Suppressor Proteins
  • Xenopus Proteins
  • transient receptor potential cation channel, subfamily C, member 1
  • Netrin-1