Inositol trisphosphate receptors:: Ca2+-modulated intracellular Ca2+ channels

被引:134
作者
Taylor, CW [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 1998年 / 1436卷 / 1-2期
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
inositol trisphosphate receptor; Ca2+ mobilization; Ca2+ channel; Ca2+ regulation; calmodulin;
D O I
10.1016/S0005-2760(98)00122-2
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 three subtypes of inositol trisphosphate (InsP(3)) receptor expressed in mammalian cells are each capable of forming intracellular Ca2+ channels that are regulated by both InsP(3) and cytosolic Ca2+. The InsP(3) receptors of many, though perhaps not all, tissues are biphasically regulated by cytosolic Ca2+: a rapid stimulation of the receptors by modest increases in Ca2+ concentration is followed by a slower inhibition at higher Ca2+ concentrations. Despite the widespread occurrence of this form of regulation and the belief that it is an important element of the mechanisms responsible for the complex Ca2+ signals evoked by physiological stimuli, the underlying mechanisms are not understood. Both accessory proteins and Ca2+-binding sites on InsP(3) receptors themselves have been proposed to mediate the effects of cytosolic Ca2+ on InsP(3) receptor function, bur the evidence is equivocal. The effects of cytosolic Ca2+ on InsP(3) binding and channel opening, and the possible means whereby the effects are mediated are discussed in this review. (C) 1998 Elsevier Science B.V. All rights reserved.
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页码:19 / 33
页数:15
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