| Literature DB >> 27818173 |
Heather N Turner1, Kevin Armengol2, Atit A Patel3, Nathaniel J Himmel3, Luis Sullivan2, Srividya Chandramouli Iyer2, Surajit Bhattacharya3, Eswar Prasad R Iyer2, Christian Landry4, Michael J Galko5, Daniel N Cox6.
Abstract
The basic mechanisms underlying noxious cold perception are not well understood. We developed Drosophila assays for noxious cold responses. Larvae respond to near-freezing temperatures via a mutually exclusive set of singular behaviors-in particular, a full-body contraction (CT). Class III (CIII) multidendritic sensory neurons are specifically activated by cold and optogenetic activation of these neurons elicits CT. Blocking synaptic transmission in CIII neurons inhibits CT. Genetically, the transient receptor potential (TRP) channels Trpm, NompC, and Polycystic kidney disease 2 (Pkd2) are expressed in CIII neurons, where each is required for CT. Misexpression of Pkd2 is sufficient to confer cold responsiveness. The optogenetic activation level of multimodal CIII neurons determines behavioral output, and visualization of neuronal activity supports this conclusion. Coactivation of cold- and heat-responsive sensory neurons suggests that the cold-evoked response circuitry is dominant. Our Drosophila model will enable a sophisticated molecular genetic dissection of cold nociceptive genes and circuits. Copyright ÂEntities:
Keywords: Drosophila; TRP channels; behavior; multimodal sensory processing; nociception; noxious cold
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Year: 2016 PMID: 27818173 PMCID: PMC5140760 DOI: 10.1016/j.cub.2016.09.038
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834