Raghu Padinjat, Hardie Roger C
Inositide Laboratory, Babraham Institute, Cambridge, United Kingdom.
Cell Calcium. 2009 Jun;45(6):566-73. doi: 10.1016/j.ceca.2009.03.005. Epub 2009 Apr 11.
The Drosophila TRPC channels TRP and TRPL are the founding members of the TRP superfamily of ion channels, which are important components of calcium influx pathways in virtually all cells. The activation of these channels in the context of fly phototransduction is one of the few in vivo models for TRPC channel activation and has served as a paradigm for understanding TRPC function. TRP and TRPL are activated by G-protein coupled PIP(2) hydrolysis through a mechanism in which IP(3) receptor mediated calcium release seems dispensable. Recent analysis has provided compelling evidence that one or more PIP(2) generated lipid messengers, as well as PIP(2) itself, are essential for regulating TRP and TRPL activity. Evidence on the role of these lipid elements in regulating TRP and TRPL activity is discussed in this review.
果蝇的瞬时受体电位通道(TRPC)TRP和TRPL是TRP离子通道超家族的创始成员,几乎在所有细胞中都是钙内流途径的重要组成部分。在果蝇光转导过程中这些通道的激活是TRPC通道激活的少数体内模型之一,并且已成为理解TRPC功能的范例。TRP和TRPL通过G蛋白偶联的磷脂酰肌醇-4,5-二磷酸(PIP(2))水解而激活,其机制中肌醇-1,4,5-三磷酸(IP(3))受体介导的钙释放似乎并非必需。最近的分析提供了令人信服的证据,表明一种或多种由PIP(2)产生的脂质信使以及PIP(2)本身对于调节TRP和TRPL活性至关重要。本综述讨论了这些脂质成分在调节TRP和TRPL活性中的作用证据。