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CRAC 通道 pore 组件 Orai1 的分子调控。

Molecular regulation of the pore component of CRAC channels, Orai1.

机构信息

Department of Physiology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.

出版信息

Curr Top Membr. 2013;71:181-207. doi: 10.1016/B978-0-12-407870-3.00008-1.

Abstract

Store-operated Ca(2+) entry (SOCE) is a fundamental mechanism ubiquitously employed by cells to elevate intracellular Ca(2+) concentrations ([Ca(2+)]i). Increased intracellular Ca(2+) ions act as a second messenger that can stimulate a variety of downstream signaling pathways affecting proliferation, secretion, differentiation, and death of cells. In immune cells, immune receptor stimulation induces endoplasmic reticulum Ca(2+) store depletion that subsequently activates Ca(2+)-release-activated-Ca(2+) (CRAC) channels, a prototype of store-operated Ca(2+) (SOC) channels. Identification of Orai1 as the pore subunit of CRAC channels has provided the much-needed molecular tool to dissect the mechanism of activation and regulation of these channels. In this review, we discuss the recent advances in understanding the regulatory mechanisms and posttranslational modifications that regulate diverse aspects of CRAC channel function.

摘要

钙库操纵性钙内流(SOCE)是细胞普遍采用的一种基本机制,用于提升细胞内钙离子浓度([Ca(2+)]i)。增加的细胞内钙离子作为第二信使,可以刺激多种下游信号通路,影响细胞的增殖、分泌、分化和死亡。在免疫细胞中,免疫受体刺激诱导内质网钙离子储存耗竭,随后激活钙释放激活钙(CRAC)通道,这是钙库操纵性钙(SOC)通道的原型。Orai1 被鉴定为 CRAC 通道的孔亚基,为解析这些通道的激活和调节机制提供了急需的分子工具。在这篇综述中,我们讨论了理解调节机制和翻译后修饰的最新进展,这些修饰调节了 CRAC 通道功能的各个方面。

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