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瞬时受体电位通道 TRPM8 通过 α2A 肾上腺素能受体信号通路被抑制。

The transient receptor potential channel TRPM8 is inhibited via the alpha 2A adrenoreceptor signaling pathway.

机构信息

INSERM U800, Equipe Labellisée par la Ligue Nationale contre le Cancer, Université des Sciences et Technologies de Lille (USTL), F59655 Villeneuve d'Ascq, France.

Bogomoletz Institute of Physiology and International Center of Molecular Physiology of the National Academy of Sciences of Ukraine, Kyiv, Ukraine.

出版信息

J Biol Chem. 2010 Mar 26;285(13):9410-9419. doi: 10.1074/jbc.M109.069377. Epub 2010 Jan 28.

Abstract

The transient receptor potential channel melastatin member 8 (TRPM8) is expressed in sensory neurons, where it constitutes the main receptor of environmental innocuous cold (10-25 degrees C). Among several types of G protein-coupled receptors expressed in sensory neurons, G(i)-coupled alpha 2A-adrenoreceptor (alpha 2A-AR), is known to be involved in thermoregulation; however, the underlying molecular mechanisms remain poorly understood. Here we demonstrated that stimulation of alpha 2A-AR inhibited TRPM8 in sensory neurons from rat dorsal root ganglia (DRG). In addition, using specific pharmacological and molecular tools combined with patch-clamp current recordings, we found that in heterologously expressed HEK-293 (human embryonic kidney) cells, TRPM8 channel is inhibited by the G(i) protein/adenylate cyclase (AC)/cAMP/protein kinase A (PKA) signaling cascade. We further identified the TRPM8 S9 and T17 as two key PKA phosphorylation sites regulating TRPM8 channel activity. We therefore propose that inhibition of TRPM8 through the alpha 2A-AR signaling cascade could constitute a new mechanism of modulation of thermosensation in both physiological and pathological conditions.

摘要

瞬时受体电位阳离子通道亚家族 M 成员 8(TRPM8)在感觉神经元中表达,在这些神经元中它构成了环境无害冷(10-25 摄氏度)的主要受体。在感觉神经元中表达的几种类型的 G 蛋白偶联受体中,G(i)-偶联的α2A-肾上腺素受体(α2A-AR)已知参与体温调节;然而,其潜在的分子机制仍知之甚少。在这里,我们证明了α2A-AR 的刺激抑制了来自大鼠背根神经节(DRG)的感觉神经元中的 TRPM8。此外,使用特定的药理学和分子工具结合膜片钳电流记录,我们发现,在异源表达的 HEK-293(人胚肾)细胞中,TRPM8 通道被 G(i)蛋白/腺苷酸环化酶(AC)/cAMP/蛋白激酶 A(PKA)信号级联抑制。我们进一步确定了 TRPM8 的 S9 和 T17 作为调节 TRPM8 通道活性的两个关键 PKA 磷酸化位点。因此,我们提出通过α2A-AR 信号级联抑制 TRPM8 可能构成在生理和病理条件下调节热感觉的新机制。

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