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钙信号转导重构与疾病。

Calcium signalling remodelling and disease.

机构信息

Babraham Institute, Babraham, Cambridge CB22 3AT, U.K.

出版信息

Biochem Soc Trans. 2012 Apr;40(2):297-309. doi: 10.1042/BST20110766.

Abstract

A wide range of Ca2+ signalling systems deliver the spatial and temporal Ca2+ signals necessary to control the specific functions of different cell types. Release of Ca2+ by InsP3 (inositol 1,4,5-trisphosphate) plays a central role in many of these signalling systems. Ongoing transcriptional processes maintain the integrity and stability of these cell-specific signalling systems. However, these homoeostatic systems are highly plastic and can undergo a process of phenotypic remodelling, resulting in the Ca2+ signals being set either too high or too low. Such subtle dysregulation of Ca2+ signals have been linked to some of the major diseases in humans such as cardiac disease, schizophrenia, bipolar disorder and Alzheimer's disease.

摘要

广泛的 Ca2+ 信号系统传递空间和时间 Ca2+ 信号,以控制不同细胞类型的特定功能。InsP3(肌醇 1,4,5-三磷酸)释放 Ca2+ 在许多这些信号系统中起着核心作用。持续的转录过程维持这些细胞特异性信号系统的完整性和稳定性。然而,这些同源平衡系统具有高度的可塑性,可以经历表型重塑的过程,导致 Ca2+ 信号过高或过低。这种 Ca2+ 信号的微妙失调与人类的一些主要疾病有关,如心脏病、精神分裂症、双相情感障碍和阿尔茨海默病。

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