Specific roles for DEG/ENaC and TRP channels in touch and thermosensation in C. elegans nociceptors

Marios Chatzigeorgiou (1) , Sungjae Yoo (1) , Joseph Watson (1) , Weihsiang Lee (1) , W. Clay Spencer (1) , Katie S Kindt (1) , Sun Wook Hwang (1) , David M Miller (1) , Millet Treinin (1) , Monica M Driscoll (1) , William R. Schafer (1)

1 Division of Cell Biology

Polymodal nociceptors detect noxious stimuli including harsh touch, toxic chemicals, and extremes of heat and cold. The molecular mechanisms by which nociceptors are able to sense multiple qualitatively distinct stimuli are not well-understood. We show here that the C. elegans PVD neurons are mulitidendritic nociceptors that respond to harsh touch as well as cold temperatures. The harsh touch modality specifically requires the DEG/ENaC proteins MEC-10 and DEGT-1, which represent putative components of a harsh touch mechanotransduction complex. By contrast, responses to cold require the TRPA-1 channel and are MEC-10- and DEGT-1-independent. Heterologous expression of C. elegans TRPA-1 can confer cold responsiveness to other C. elegans neurons or to mammalian cells, indicating that TRPA-1 is itself a cold sensor. These results show that C. elegans nociceptors respond to thermal and mechanical stimuli using distinct sets of molecules, and identify DEG/ENaC channels as potential receptors for mechanical pain.

Mots clés: Behaviour; Neuroimaging; Pain; Sensory Transduction

Marios Chatzigeorgiou, Sungjae Yoo, Joseph Watson, Weihsiang Lee, W. Clay Spencer, et al.. Specific roles for DEG/ENaC and TRP channels in touch and thermosensation in C. elegans nociceptors. Nature Neuroscience, 2010, ⟨10.1038/nn.2581⟩. ⟨hal-00541161⟩