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Cited 193 time in webofscience Cited 185 time in scopus
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Species differences and molecular determinant of TRPA1 cold sensitivityopen access

Authors
Chen, JunKang, DawonXu, JingLake, MarcHogan, James O.Sun, ChaohongWalter, KarlYao, BettyKim, Donghee
Issue Date
Sep-2013
Publisher
NATURE PUBLISHING GROUP
Citation
NATURE COMMUNICATIONS, v.4
Indexed
SCIE
SCOPUS
Journal Title
NATURE COMMUNICATIONS
Volume
4
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/20496
DOI
10.1038/ncomms3501
ISSN
2041-1723
Abstract
TRPA1 is an ion channel and has been proposed as a thermosensor across species. In invertebrate and ancestral vertebrates such as fly, mosquito, frog, lizard and snakes, TRPA1 serves as a heat receptor, a sensory input utilized for heat avoidance or infrared detection. However, in mammals, whether TRPA1 is a receptor for noxious cold is highly controversial, as channel activation by cold was observed by some groups but disputed by others. Here we attribute the discrepancy to species differences. We show that cold activates rat and mouse TRPA1 but not human or rhesus monkey TRPA1. At the molecular level, a single residue within the S5 transmembrane domain (G878 in rodent but V875 in primate) accounts for the observed difference in cold sensitivity. This residue difference also underlies the species-specific effects of menthol. Together, our findings identify the species-specific cold activation of TRPA1 and reveal a molecular determinant of cold-sensitive gating.
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