sumo酰化和钙信号传导:在大脑内外的潜在作用。

Q4 Neuroscience
Neuronal signaling Pub Date : 2017-07-19 eCollection Date: 2017-08-01 DOI:10.1042/NS20160010
Leticia Coelho-Silva, Gary J Stephens, Helena Cimarosti
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引用次数: 7

摘要

小泛素样修饰物(Small ubiquitin-like modifier, SUMO)偶联(SUMOylation)是一种涉及蛋白质表达、定位和功能改变的翻译后蛋白质修饰。尽管SUMO的许多核作用已被很好地表征,但这一过程仅开始与膜蛋白(如离子通道)相关的探索。钙离子(Ca2+)信号对细胞的正常功能至关重要,也参与相关神经和心血管疾病的病理生理机制。细胞内Ca2+水平受到严格调控;休息时,大多数Ca2+保留在细胞器中,如肌浆网或细胞外空间,而去极化触发一系列事件,导致Ca2+进入,随后是挤压和再摄取。维持Ca2+平衡的机制是翻译后水平调节的候选机制。在这里,我们回顾了蛋白质SUMOylation的影响,包括Ca2+通道,他们的蛋白质组和其他蛋白质与Ca2+信号,对重要的细胞功能,如神经传递在中枢神经系统(CNS)和其他系统,最突出的是在这里,在心脏系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

SUMOylation and calcium signalling: potential roles in the brain and beyond.

SUMOylation and calcium signalling: potential roles in the brain and beyond.

Small ubiquitin-like modifier (SUMO) conjugation (or SUMOylation) is a post-translational protein modification implicated in alterations to protein expression, localization and function. Despite a number of nuclear roles for SUMO being well characterized, this process has only started to be explored in relation to membrane proteins, such as ion channels. Calcium ion (Ca2+) signalling is crucial for the normal functioning of cells and is also involved in the pathophysiological mechanisms underlying relevant neurological and cardiovascular diseases. Intracellular Ca2+ levels are tightly regulated; at rest, most Ca2+ is retained in organelles, such as the sarcoplasmic reticulum, or in the extracellular space, whereas depolarization triggers a series of events leading to Ca2+ entry, followed by extrusion and reuptake. The mechanisms that maintain Ca2+ homoeostasis are candidates for modulation at the post-translational level. Here, we review the effects of protein SUMOylation, including Ca2+ channels, their proteome and other proteins associated with Ca2+ signalling, on vital cellular functions, such as neurotransmission within the central nervous system (CNS) and in additional systems, most prominently here, in the cardiac system.

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来源期刊
CiteScore
4.60
自引率
0.00%
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审稿时长
14 weeks
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