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哺乳动物细胞中肌醇脂质通过多种机制对钙离子内流进行调节。

Regulation of Ca2+ entry by inositol lipids in mammalian cells by multiple mechanisms.

作者信息

Balla Tamas

机构信息

Section on Molecular Signal Transduction, Program for Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, United States.

出版信息

Cell Calcium. 2009 Jun;45(6):527-34. doi: 10.1016/j.ceca.2009.03.013. Epub 2009 Apr 22.

Abstract

Increased phosphoinositide turnover was first identified as an early signal transduction event initiated by cell surface receptors that were linked to calcium signaling. Subsequently, the generation of inositol 1,4,5-trisphosphate by phosphoinositide-specific phospholipase C enzymes was defined as the major link between inositide turnover and the cytosolic Ca(2+) rise in response to external stimulation. However, in the last decades, phosphoinositides have been emerging as major regulatory lipids involved in virtually every membrane-associated signaling process. Phosphoinositides regulate both the activity and the trafficking of almost all ion channels and transporters contributing to the maintenance of the ionic gradients that are essential for the proper functioning of all eukaryotic cells. Here we summarize the various means by which phosphoinositides affect ion channel functions with special emphasis on Ca(2+) signaling and outline the principles that govern the highly compartmentalized roles of these regulatory lipids.

摘要

磷酸肌醇代谢增加最初被确定为细胞表面受体引发的早期信号转导事件,这些受体与钙信号传导相关。随后,磷酸肌醇特异性磷脂酶C酶生成肌醇1,4,5 -三磷酸被定义为肌醇代谢与响应外部刺激时胞质Ca(2+)升高之间的主要联系。然而,在过去几十年中,磷酸肌醇已逐渐成为几乎参与每个膜相关信号传导过程的主要调节性脂质。磷酸肌醇调节几乎所有离子通道和转运蛋白的活性及运输,这些离子通道和转运蛋白有助于维持离子梯度,而离子梯度对于所有真核细胞的正常功能至关重要。在此,我们总结了磷酸肌醇影响离子通道功能的各种方式,特别强调Ca(2+)信号传导,并概述了支配这些调节性脂质高度分隔化作用的原则。

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