Calcium-sensing mechanism in TRPC5 channels contributing to retardation of neurite outgrowth.
Journal
  The Journal of physiology.
Citation
  J Physiol. 572(Pt 1):165-72
Publication date
  2006 Apr 1
Authors
  Hui H
McHugh D
Hannan M
Zeng F
Xu SZ
Khan SU
Levenson R
Beech DJ
Weiss JL
Investigators
  Robert Levenson
Grants
  Wellcome Trust
MeSH headings
  Calcium
Calcium-Binding Proteins
Ion Channel Gating
Membrane Potentials
Neurites
Neurons
Neuropeptides
TRPC Cation Channels
MeSH qualifiers
  metabolism
physiology
Abstract
  The calcium- and sodium-permeable transient receptor potential channel TRPC5 has an inhibitory role in neuronal outgrowth but the mechanisms governing its activity are poorly understood. Here we propose a mechanism involving the neuronal calcium sensor-1 (NCS-1) protein. Inhibitory mutants of TRPC5 and NCS-1 enhance neurite outgrowth similarly. Mutant NCS-1 does not inhibit surface-expression of TRPC5 but generally suppresses channel activity, irrespective of whether it is evoked by carbachol, store depletion, lanthanides or elevated intracellular calcium. NCS-1 and TRPC5 are in the same protein complex in rat brain and NCS-1 directly binds to the TRPC5 C-terminus. The data suggest protein-protein interaction between NCS-1 and TRPC5, and involvement of this protein complex in retardation of neurite outgrowth.