Human and Mouse TRPA1 Are Heat and Cold Sensors Differentially Tuned by Voltage
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F20%3A00524175" target="_blank" >RIV/67985823:_____/20:00524175 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11310/20:10420691 RIV/00216208:11320/20:10420691
Result on the web
<a href="https://www.mdpi.com/2073-4409/9/1/57" target="_blank" >https://www.mdpi.com/2073-4409/9/1/57</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/cells9010057" target="_blank" >10.3390/cells9010057</a>
Alternative languages
Result language
angličtina
Original language name
Human and Mouse TRPA1 Are Heat and Cold Sensors Differentially Tuned by Voltage
Original language description
Transient receptor potential ankyrin 1 channel (TRPA1) serves as a key sensor for reactive electrophilic compounds across all species. Its sensitivity to temperature, however, differs among species, a variability that has been attributed to an evolutionary divergence. Mouse TRPA1 was implicated in noxious cold detection but was later also identified as one of the prime noxious heat sensors. Moreover, human TRPA1, originally considered to be temperature-insensitive, turned out to act as an intrinsic bidirectional thermosensor that is capable of sensing both cold and heat. Using electrophysiology and modeling, we compare the properties of human and mouse TRPA1, and we demonstrate that both orthologues are activated by heat, and their kinetically distinct components of voltage-dependent gating are differentially modulated by heat and cold. Furthermore, we show that both orthologues can be strongly activated by cold after the concurrent application of voltage and heat. We propose an allosteric mechanism that could account for the variability in TRPA1 temperature responsiveness.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30103 - Neurosciences (including psychophysiology)
Result continuities
Project
<a href="/en/project/GA19-03777S" target="_blank" >GA19-03777S: Molecular Basis of Thermosensitive TRP Ion Channel Regulation in Nociceptive Neurons</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cells
ISSN
2073-4409
e-ISSN
—
Volume of the periodical
9
Issue of the periodical within the volume
1
Country of publishing house
CH - SWITZERLAND
Number of pages
24
Pages from-to
57
UT code for WoS article
000515398200057
EID of the result in the Scopus database
2-s2.0-85090250045