A C. elegans stretch receptor neuron revealed by a mechanosensitive TRP channel homologue

Nature. 2006 Mar 30;440(7084):684-7. doi: 10.1038/nature04538.

Abstract

The nematode Caenorhabditis elegans is commonly used as a genetic model organism for dissecting integration of the sensory and motor systems. Despite extensive genetic and behavioural analyses that have led to the identification of many genes and neural circuits involved in regulating C. elegans locomotion behaviour, it remains unclear whether and how somatosensory feedback modulates motor output during locomotion. In particular, no stretch receptors have been identified in C. elegans, raising the issue of whether stretch-receptor-mediated proprioception is used by C. elegans to regulate its locomotion behaviour. Here we have characterized TRP-4, the C. elegans homologue of the mechanosensitive TRPN channel. We show that trp-4 mutant worms bend their body abnormally, exhibiting a body posture distinct from that of wild-type worms during locomotion, suggesting that TRP-4 is involved in stretch-receptor-mediated proprioception. We show that TRP-4 acts in a single neuron, DVA, to mediate its function in proprioception, and that the activity of DVA can be stimulated by body stretch. DVA both positively and negatively modulates locomotion, providing a unique mechanism whereby a single neuron can fine-tune motor activity. Thus, DVA represents a stretch receptor neuron that regulates sensory-motor integration during C. elegans locomotion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caenorhabditis elegans / cytology*
  • Caenorhabditis elegans / physiology*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Calcium / metabolism
  • Dopamine / metabolism
  • Locomotion / genetics
  • Locomotion / physiology
  • Mechanoreceptors / metabolism*
  • Mechanotransduction, Cellular / physiology*
  • Mutation / genetics
  • Neurons / metabolism*
  • Phenotype
  • TRPC Cation Channels / genetics
  • TRPC Cation Channels / metabolism*

Substances

  • Caenorhabditis elegans Proteins
  • TRP-4 channel, C elegans
  • TRPC Cation Channels
  • Calcium
  • Dopamine