Taylor C W, Richardson A
Department of Pharmacology, Cambridge, U.K.
Pharmacol Ther. 1991;51(1):97-137. doi: 10.1016/0163-7258(91)90043-l.
Inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) is a soluble intracellular messenger formed rapidly after activation of a variety of cell-surface receptors that stimulate phosphoinositidase C activity. The initial response to Ins(1,4,5)P3 is a rapid Ca2+ efflux from nonmitochondrial intracellular stores which are probably specialized subcompartments of the endoplasmic reticulum, although their exact identities remain unknown. This initial response is followed by more complex Ca2+ signals: regenerative Ca2+ waves propagate across the cell, repetitive Ca2+ spikes occur, and stimulated Ca2+ entry across the plasma membrane contributes to the sustained Ca2+ signal. The mechanisms underlying these complex Ca2+ signals are unknown, although Ins(1,4,5)P3 is clearly involved. The intracellular receptor that mediates Ins(1,4,5)P3-stimulated Ca2+ mobilization has been purified and functionally reconstituted, and its amino acid sequence deduced from its cDNA sequence. These studies demonstrate that the Ins(1,4,5)P3 receptor has an integral Ca2+ channel separated from the Ins(1,4,5)P3 binding site by a long stretch of residues some of which form binding sites for allosteric regulators, and some of which are substrates for phosphorylation. In this review, we discuss the ligand recognition characteristics of Ins(1,4,5)P3 receptors, and their functional properties in their native environment and after purification, and we relate these properties to what is known of the structure of the receptor. In addition to regulation by Ins(1,4,5)P3, the Ins(1,4,5)P3 receptor is subject to many additional regulatory influences which include Ca2+, adenine nucleotides, pH and phosphorylation by protein kinases. Many of the functional and structural characteristics of the Ins(1,4,5)P3 receptor show striking similarities to another intracellular Ca2+ channel, the ryanodine receptor. These properties of the Ins(1,4,5)P3 are discussed, and their possible roles in contributing to the complex Ca2+ signals evoked by extracellular stimuli are considered.
肌醇1,4,5 - 三磷酸(Ins(1,4,5)P3)是一种可溶性细胞内信使,在多种刺激磷酸肌醇酶C活性的细胞表面受体激活后迅速形成。对Ins(1,4,5)P3的初始反应是Ca2+从非线粒体细胞内储存库快速外流,这些储存库可能是内质网的特殊亚区室,尽管它们的确切身份尚不清楚。这种初始反应之后是更复杂的Ca2+信号:再生性Ca2+波在细胞内传播,重复的Ca2+尖峰出现,并且刺激的Ca2+通过质膜内流有助于维持Ca2+信号。这些复杂Ca2+信号的潜在机制尚不清楚,尽管Ins(1,4,5)P3显然参与其中。介导Ins(1,4,5)P3刺激的Ca2+动员的细胞内受体已被纯化并进行了功能重建,其氨基酸序列也从其cDNA序列推导得出。这些研究表明,Ins(1,4,5)P3受体有一个完整的Ca2+通道,该通道与Ins(1,4,5)P3结合位点由一长串残基隔开,其中一些残基形成变构调节剂的结合位点,一些残基是磷酸化的底物。在这篇综述中,我们讨论了Ins(1,4,5)P3受体的配体识别特性,以及它们在天然环境和纯化后的功能特性,并将这些特性与已知的受体结构联系起来。除了受Ins(1,4,5)P3调节外,Ins(1,4,5)P3受体还受到许多其他调节影响,包括Ca2+、腺嘌呤核苷酸、pH以及蛋白激酶的磷酸化。Ins(1,4,5)P3受体的许多功能和结构特征与另一种细胞内Ca2+通道——兰尼碱受体有显著相似之处。本文讨论了Ins(1,4,5)P3的这些特性,并考虑了它们在促成细胞外刺激诱发的复杂Ca2+信号中可能发挥的作用。