Ca2+ Channels on the Move

被引:38
|
作者
Taylor, Colin W. [1 ]
Prole, David L. [1 ]
Rahman, Taufiq [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1PD, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; PANCREATIC BETA-CELLS; SMOOTH-MUSCLE-CELLS; MESSENGER-RNA LOCALIZATION; POTENTIAL CATION CHANNELS; CALCIUM-RELEASE CHANNEL; CYCLIC ADP-RIBOSE; FLUORESCENT PROTEIN INDICATORS; NUCLEOTIDE-GATED CHANNEL; ACTIVATES CRAC CHANNELS;
D O I
10.1021/bi901739t
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The versatility of Ca2+ its an intracellular messenger derives largely from the spatial organization of cytosolic Ca2+ signals, most of which are generated by regulated openings of Ca2+-permeable channels. Most Ca2+ channels are expressed in the plasma membrane (PM). Others, including the almost ubiquitous inositol 1,4,5-trisphosphate receptors (IP3R) and their relatives, the ryanodine receptors (RyR), are predominantly expressed in membranes of the sarcoplasmic or endoplasmic reticulum (ER). Targeting of these channels to appropriate destinations underpins their ability to generate spatially organized Ca2+ signals. All Ca2+ channels begin life in the cytosol, and the vast majority are then functionally assembled in the ER, where they may either remain or be dispatched to other membranes. Here, by means of selective examples, we review two issues related to this trafficking of Ca2+ channels via the ER. How do cells avoid wayward activity of Ca2+ channels in transit as they pass from the ER via other membranes to their final destination? How and why do some cells express small numbers of the archetypal intracellular Ca2+ channels, IP3R and RyR, in the PM?
引用
收藏
页码:12062 / 12080
页数:19
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