Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University, Providence, RI, USA.
Adv Exp Med Biol. 2011;704:135-45. doi: 10.1007/978-94-007-0265-3_7.
TRPM1, initially named Melastatin, is the founding member of the TRPM subfamily of Transient Receptor Potential (TRP) ion channels. Despite sustained efforts, the molecular properties and physiological functions of TRPM1 remained elusive until recently. New evidence has uncovered novel TRPM1 splice variants and revealed that TRPM1 is critical for a non-selective cation conductance in melanocytes and retinal bipolar cells. Functionally, TRPM1 has been shown to mediate retinal ON bipolar cell transduction and suggested to regulate melanocyte pigmentation. Notably, TRPM1 mutations have also been associated with congenital stationary night blindness in humans. This review will summarize and discuss our present knowledge of TRPM1: its discovery, expression, regulation, and proposed functions in skin and eye.
TRPM1,最初名为 Melastatin,是 Transient Receptor Potential (TRP) 离子通道的 TRPM 亚家族的创始成员。尽管进行了持续的努力,但直到最近,TRPM1 的分子特性和生理功能仍然难以捉摸。新的证据揭示了新的 TRPM1 剪接变体,并表明 TRPM1 对于黑色素细胞和视网膜双极细胞中的非选择性阳离子电导至关重要。在功能上,已经表明 TRPM1 介导视网膜 ON 双极细胞转导,并提示调节黑色素细胞的色素沉着。值得注意的是,TRPM1 突变也与人类先天性静止性夜盲症有关。本综述将总结和讨论我们目前对 TRPM1 的了解:它的发现、表达、调节以及在皮肤和眼睛中的拟议功能。