-
Something wrong with this record ?
Cellular context determines primary characteristics of human TRPC5 as a cold-activated channel
A. Ptakova, M. Mitro, L. Zimova, V. Vlachova
Language English Country United States
Document type Journal Article
Grant support
GAUK 297921
Grantová Agentura, Univerzita Karlova
GACR 22-13750S
Grantová Agentura Ceské Republiky
PubMed
35762104
DOI
10.1002/jcp.30821
Knihovny.cz E-resources
- MeSH
- Cell Membrane metabolism MeSH
- HEK293 Cells MeSH
- TRPC Cation Channels * genetics metabolism MeSH
- Humans MeSH
- Calcium * metabolism MeSH
- Calcium Channels metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
The human transient receptor potential canonical 5 (TRPC5) is a calcium-permeable, nonselective cation channel expressed in the central and peripheral nervous system and also in other tissues such as the kidney, synovium, and odontoblasts. TRPC5 has been recently confirmed to play a key role in spontaneous, inflammatory mechanical, and cold pain. Although TRPC5 activation is known to be cold sensitive, it is unclear whether this property is intrinsic to the channel protein and whether or to what extent it may be determined by the cellular environment. In this study, we explored the cold sensitivity of human TRPC5 at the single-channel level using transiently transfected HEK293T cells. Upon decreasing the temperature, the channel demonstrated prolonged mean open dwell times and a robust increase in the open probability (Po ), whereas the amplitude of unitary currents decreased ~1.5-fold per 10°C of temperature difference. In the absence of any agonists, the temperature dependence of Po was sigmoidal, with a steep slope within the temperature range of 16°C-11°C, and exhibited saturation below 8-5°C. Thermodynamic analysis revealed significant changes in enthalpy and entropy, suggesting that substantial conformational changes accompany cold-induced gating. The mutant channel T970A, in which the regulation downstream of G-protein coupled receptor signaling was abrogated, exhibited higher basal activity at room temperature and a less steep temperature response profile, with an apparent threshold below 22°C. An even more pronounced decrease in the activation threshold was observed in a mutant that disrupted the electrostatic interaction of TRPC5 with the endoplasmic reticulum calcium sensor stromal interaction molecule 1. Thus, TRPC5 exhibits features of an intrinsically cold-gated channel; its sensitivity to cold tightly depends on the phosphorylation status of the protein and intracellular calcium homeostasis.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22024600
- 003
- CZ-PrNML
- 005
- 20221031101053.0
- 007
- ta
- 008
- 221017s2022 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1002/jcp.30821 $2 doi
- 035 __
- $a (PubMed)35762104
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Ptakova, Alexandra $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, Prague, Czech Republic $u Department of Physiology, Faculty of Science, Charles University, Prague, Czech Republic
- 245 10
- $a Cellular context determines primary characteristics of human TRPC5 as a cold-activated channel / $c A. Ptakova, M. Mitro, L. Zimova, V. Vlachova
- 520 9_
- $a The human transient receptor potential canonical 5 (TRPC5) is a calcium-permeable, nonselective cation channel expressed in the central and peripheral nervous system and also in other tissues such as the kidney, synovium, and odontoblasts. TRPC5 has been recently confirmed to play a key role in spontaneous, inflammatory mechanical, and cold pain. Although TRPC5 activation is known to be cold sensitive, it is unclear whether this property is intrinsic to the channel protein and whether or to what extent it may be determined by the cellular environment. In this study, we explored the cold sensitivity of human TRPC5 at the single-channel level using transiently transfected HEK293T cells. Upon decreasing the temperature, the channel demonstrated prolonged mean open dwell times and a robust increase in the open probability (Po ), whereas the amplitude of unitary currents decreased ~1.5-fold per 10°C of temperature difference. In the absence of any agonists, the temperature dependence of Po was sigmoidal, with a steep slope within the temperature range of 16°C-11°C, and exhibited saturation below 8-5°C. Thermodynamic analysis revealed significant changes in enthalpy and entropy, suggesting that substantial conformational changes accompany cold-induced gating. The mutant channel T970A, in which the regulation downstream of G-protein coupled receptor signaling was abrogated, exhibited higher basal activity at room temperature and a less steep temperature response profile, with an apparent threshold below 22°C. An even more pronounced decrease in the activation threshold was observed in a mutant that disrupted the electrostatic interaction of TRPC5 with the endoplasmic reticulum calcium sensor stromal interaction molecule 1. Thus, TRPC5 exhibits features of an intrinsically cold-gated channel; its sensitivity to cold tightly depends on the phosphorylation status of the protein and intracellular calcium homeostasis.
- 650 12
- $a vápník $x metabolismus $7 D002118
- 650 _2
- $a vápníkové kanály $x metabolismus $7 D015220
- 650 _2
- $a buněčná membrána $x metabolismus $7 D002462
- 650 _2
- $a HEK293 buňky $7 D057809
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a kationtové kanály TRPC $x genetika $x metabolismus $7 D050052
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Mitro, Michal $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, Prague, Czech Republic $u Department of Physiology, Faculty of Science, Charles University, Prague, Czech Republic
- 700 1_
- $a Zimova, Lucie $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Vlachova, Viktorie $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, Prague, Czech Republic $1 https://orcid.org/http://orcid.org/0000000286210935
- 773 0_
- $w MED00009981 $t Journal of cellular physiology $x 1097-4652 $g Roč. 237, č. 9 (2022), s. 3614-3626
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/35762104 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20221017 $b ABA008
- 991 __
- $a 20221031101050 $b ABA008
- 999 __
- $a ok $b bmc $g 1854366 $s 1175890
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2022 $b 237 $c 9 $d 3614-3626 $e 20220627 $i 1097-4652 $m Journal of cellular physiology $n J Cell Physiol $x MED00009981
- GRA __
- $a GAUK 297921 $p Grantová Agentura, Univerzita Karlova
- GRA __
- $a GACR 22-13750S $p Grantová Agentura Ceské Republiky
- LZP __
- $a Pubmed-20221017