Regulation of Drosophila TRPC channels by protein and lipid interactions

被引:9
作者
Raghu, Padinjat [1 ]
机构
[1] Babraham Inst, Inositide Lab, Cambridge CB2 4AT, England
基金
英国生物技术与生命科学研究理事会;
关键词
diacylglycerol kinase; PI(4,5)P-2; INAD; calcium; degeneration;
D O I
10.1016/j.semcdb.2006.11.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Drosophila TRPC channels TRP and TRPL are the founding members of the TRP superfamily of ion channels, proteins likely to be important components of calcium influx pathways. 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 PI(4,5)P-2 hydrolysis through a mechanism in which IP3 receptor mediated calcium release seems dispensable. Recent analysis has provided compelling evidence that the accurate turnover of PI(4,5)P-2 generated lipid messengers in essential for regulating TRP and TRPL activity. TRP channels also appear to exist in the context of a macromolecular complex containing key components involved in activation such as phospholipase C beta and protein kinase C. This complex may be important for activation. The role of these protein and lipid elements in regulating TRP and TRPL activity is discussed in this review. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:646 / 653
页数:8
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