Journal
CHANNELS
Volume 7, Issue 2, Pages 115-118Publisher
LANDES BIOSCIENCE
DOI: 10.4161/chan.23466
Keywords
TRPM8; heterotrimeric G proteins; GPCR; cold; pain
Categories
Funding
- MRC new investigator grant [G0801387]
- Medical Research Council [G0801387] Funding Source: researchfish
- MRC [G0801387] Funding Source: UKRI
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Cold temperature is encoded by the cold-sensitive ion channel TRPM8 in somatosensory neurons. It has been unclear how TRPM8 is modulated so that it can mediate distinct type of cold signaling. We have recently reported that activated G alpha(q) directly inhibits TRPM8 after activation of Gq-coupled receptors. Here, we further show that activation of the muscarinic receptor M1R, which is known to inhibit M currents through PLC-mediated hydrolysis of PtdIns(4,5)P-2, similarly inhibited TRPM8 potently, but inhibition was not prevented by the PLC inhibitor U73122. Interestingly, although G alpha(q) and G alpha(11) are indistinguishable in activating PLC and hydrolysing PtdIns(4,5)P-2, activated G alpha(11) inhibited TRPM8 to a lesser extent than activated G(q). The differential TRPM8 inhibition is determined by a specific residue E197 on G alpha(11), because mutating this residue to the corresponding residue on G alpha(q) restored TRPM8 inhibition to a similar degree as mediated by G alpha(q). These results reinforce the idea that activated G alpha(q) directly inhibits TRPM8 independently from PtdIns(4,5)P-2 hydrolysis-mediated inhibition of TRPM8.
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