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平面脂双层中冷和化学激动剂激活的瞬时受体电位 melastatin 8(TRPM8)通道的门控。

Gating of transient receptor potential melastatin 8 (TRPM8) channels activated by cold and chemical agonists in planar lipid bilayers.

机构信息

Department of Pharmacology and Physiology, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, New Jersey 07103, USA.

出版信息

J Neurosci. 2010 Sep 15;30(37):12526-34. doi: 10.1523/JNEUROSCI.3189-10.2010.

Abstract

The transient receptor potential melastatin 8 (TRPM8) ion channel is a major sensor of environmental cold temperatures. It is activated by cold and chemical agonists, such as menthol and icilin. The activation of these channels both by cold and cooling agents requires the presence of the membrane phospholipid phosphatidylinositol 4,5-bisphosphate [PI(4,5)P(2)]. The mechanism of TRPM8 activation by physical and chemical factors is unknown, and the involvement of cellular signaling pathways has been considered. Here we have characterized the gating mechanism of the rat TRPM8 reconstituted in planar lipid bilayers and its activation by different stimuli. In this system, the influence of cellular signaling pathways can be excluded. We found that TRPM8 activated by cold exhibits steep temperature dependence [temperature coefficient (Q(10)) of ∼40], and the channel openings are accompanied by large changes in entropy and enthalpy, suggesting a substantial conformation change. TRPM8 channel behavior upon menthol and icilin activation was distinguishable, and the effect of icilin depended on the presence of calcium on the intracellular side of the protein. Here we also demonstrate that PI(4,5)P(2) is the prime factor that impacts the gating of TRPM8 and that other phosphoinositides are less efficient in supporting channel activity. Menthol increases the potency of PI(4,5)P(2) to activate the channels and increases binding of phosphoinositides to the full-length channel protein. Our data demonstrate conclusively that TRPM8 is gated by cold and its chemical agonists directly, and that dependence of its gating on PI(4,5)P(2) is a result of direct specific interactions with the lipid.

摘要

瞬时受体电位 melastatin 8 (TRPM8) 离子通道是环境冷温度的主要传感器。它被冷和化学激动剂如薄荷醇和异丁香酚激活。这些通道的激活无论是通过冷还是冷却剂,都需要膜磷脂酰肌醇 4,5-二磷酸 [PI(4,5)P(2)] 的存在。TRPM8 被物理和化学因素激活的机制尚不清楚,并且已经考虑了细胞信号通路的参与。在这里,我们已经描述了在平面脂质双层中重组的大鼠 TRPM8 的门控机制及其对不同刺激的激活。在这个系统中,可以排除细胞信号通路的影响。我们发现,冷激活的 TRPM8 表现出陡峭的温度依赖性[约 40 的温度系数 (Q(10))],并且通道开放伴随着熵和焓的巨大变化,表明发生了实质性的构象变化。薄荷醇和异丁香酚激活的 TRPM8 通道行为是可区分的,并且异丁香酚的作用取决于蛋白细胞内侧面的钙存在。在这里,我们还证明了 PI(4,5)P(2) 是影响 TRPM8 门控的主要因素,而其他磷酸肌醇在支持通道活性方面效率较低。薄荷醇增加了 PI(4,5)P(2) 激活通道的效力,并增加了磷酸肌醇与全长通道蛋白的结合。我们的数据明确证明了 TRPM8 被冷及其化学激动剂直接门控,并且其门控对 PI(4,5)P(2) 的依赖性是与脂质直接特异性相互作用的结果。

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