瞬时受体电位M8离子通道功能及其翻译后修饰调节机制

瞬时受体电位M8(transient receptor potential melastatin 8, TRPM8)又称冷及薄荷醇感受器,位于细胞膜或细胞器膜上,是瞬时受体电位(transient receptor potential, TRP)通道超家族中的一员。TRPM8通道分布广泛,是一个非选择性阳离子通道,可作为冷热传感器和冷痛传感器进行信号传导,参与众多生物过程的调节,在维持细胞内外稳态、控制离子进出细胞方面具有重要作用。研究发现,蛋白质翻译后修饰(post-translational modification, PTM)通过调控TRPM8通道的功能,进而影响多种疾病的发生和发展。因此,探究TRPM8的翻译后修饰的过程,对深入了解TRPM8的功能及调控机制是十分必要的。目前,已报道的TRPM8翻译后修饰包括磷酸化、泛素化和糖基化等,它们能够调控蛋白质的相互作用和改变TRPM8离子通道的活性,从而调控细胞增殖、迁移和凋亡。值得注意的是,TRPM8的表达与前列腺癌、膀胱癌和乳腺癌等多种癌症密切相关。本文将从TRPM8离子通道的结构出发,系统地阐述TRPM8蛋白翻译后修饰和激动剂、拮抗剂以及一些蛋白质对TRPM8通道活性的调节,同时总结TRPM8在前列腺癌、膀胱癌和乳腺癌中的新进展,为癌症治疗提供新方向和新思路。

Function of TRPM8 Ion Channel and Regulation Mechanism of Its Post-translational Modification

TRPM8 (transient receptor potential melastatin 8), also known as a cold and menthol receptor and a member of the TRP (transient receptor potential) channel superfamily, locates on the cell membrane or organelle membrane. . TRPM8 is a non-selective cation channel, which can be used as either a cold and heat sensor or cold and pain sensor to conduct signal transduction. It plays an important role in maintaining intracellular homeostasis and controlling ion in cells. It has been found that PTM (post-translational modification) of TRPM8 affects the occurrence and development of many diseases by regulating the function of TRPM8 channel. Therefore, it is necessary to explore the PTM process of TRPM8 to gain a deeper understanding for the function and regulatory mechanism of TRPM8. At present, several types of post-translational modifications of TRPM8 have been reported, including phosphorylation, ubiquitination and glycosylation, which can regulate protein interactions and change the activity of TRPM8 ion channels, leading to modulation of cell proliferation, migration and apoptosis. It is noteworthy that the expression of TRPM8 level is closely related to many kinds of cancers, such as prostate cancer, bladder cancer and breast cancer. This review focus on the structure of TRPM8 ion channels, systematically elaborate the translational modifications, activator and antagonist of TRPM8 protein, and the regulation of some proteins on TRPM8 channel activity. At the same time, we summarize the recent progress of TRPM8 in prostate cancer, bladder cancer and breast cancer, which would provide new directions and new ideas for the treatment of cancer.