Department of Pharmacology, University of Cambridge, Cambridge, UK.
Channels (Austin). 2013 Mar-Apr;7(2):115-8. doi: 10.4161/chan.23466. Epub 2013 Jan 18.
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 Gαq 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 PLCβ-mediated hydrolysis of PtdIns(4,5)P 2, similarly inhibited TRPM8 potently, but inhibition was not prevented by the PLC inhibitor U73122. Interestingly, although Gαq and Gα 11 are indistinguishable in activating PLCβ and hydrolysing PtdIns(4,5)P 2, activated Gα 11 inhibited TRPM8 to a lesser extent than activated Gαq. The differential TRPM8 inhibition is determined by a specific residue E197 on Gα 11, because mutating this residue to the corresponding residue on Gαq restored TRPM8 inhibition to a similar degree as mediated by Gαq. These results reinforce the idea that activated Gαq directly inhibits TRPM8 independently from PtdIns(4,5)P 2 hydrolysis-mediated inhibition of TRPM8.
低温由感觉神经元中的冷敏感离子通道 TRPM8 编码。目前尚不清楚 TRPM8 是如何被调节的,以便它能够介导不同类型的冷信号。我们最近报道说,Gq 偶联受体激活后,激活的 Gαq 可直接抑制 TRPM8。在这里,我们进一步表明,毒蕈碱受体 M1R 的激活,已知通过 PLCβ 介导的 PtdIns(4,5)P 2 水解来抑制 M 电流,同样强烈抑制 TRPM8,但抑制作用不能被 PLC 抑制剂 U73122 阻止。有趣的是,尽管 Gαq 和 Gα 11 在激活 PLCβ 和水解 PtdIns(4,5)P 2 方面没有区别,但激活的 Gα 11 对 TRPM8 的抑制作用程度低于激活的 Gαq。这种差异抑制作用由 Gα 11 上的特定残基 E197 决定,因为将该残基突变为 Gαq 上的相应残基,可将 TRPM8 抑制作用恢复到与 Gαq 介导的相似程度。这些结果强化了这样一种观点,即激活的 Gαq 可直接抑制 TRPM8,而不依赖于 PtdIns(4,5)P 2 水解介导的 TRPM8 抑制。