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管腔内钙作为内质网功能的主要调节因子。

Intraluminal calcium as a primary regulator of endoplasmic reticulum function.

作者信息

Burdakov Denis, Petersen Ole H, Verkhratsky Alexei

机构信息

Faculty of Life Sciences, The University of Manchester, 1.124 Stopford Building, Oxford Road, Manchester M13 9PT, UK.

出版信息

Cell Calcium. 2005 Sep-Oct;38(3-4):303-10. doi: 10.1016/j.ceca.2005.06.010.

DOI:10.1016/j.ceca.2005.06.010
PMID:16076486
Abstract

The concentration of Ca2+ inside the lumen of endoplasmic reticulum (ER) regulates a vast array of spatiotemporally distinct cellular processes, from intracellular Ca2+ signals to intra-ER protein processing and cell death. This review summarises recent data on the mechanisms of luminal Ca2+-dependent regulation of Ca2+ release and uptake as well as ER regulation of cellular adaptive processes. In addition we discuss general biophysical properties of the ER membrane, as trans-endomembrane Ca2+ fluxes are subject to basic electrical forces, determined by factors such as the membrane potential of the ER and the ease with which Ca2+ fluxes are able to change this potential (i.e. the resistance of the ER membrane). Although these electrical forces undoubtedly play a fundamental role in shaping Ca2+ dynamics, at present there is very little direct experimental information about the biophysical properties of the ER membrane. Further studies of how intraluminal [Ca2+] is regulated, best carried out with direct measurements, are vital for understanding how Ca2+ orchestrates cell function. Direct monitoring of Ca2+ under conditions where the cytosolic [Ca2+] is known may also help to capture elusive biophysical information about the ER, such as the potential difference across the ER membrane.

摘要

内质网(ER)腔内Ca2+的浓度调节着大量时空上不同的细胞过程,从细胞内Ca2+信号到内质网内蛋白质加工以及细胞死亡。本综述总结了关于内质网腔内Ca2+依赖性调节Ca2+释放和摄取机制以及内质网对细胞适应性过程调节的最新数据。此外,我们还讨论了内质网膜的一般生物物理特性,因为跨内膜Ca2+通量受到基本电力的影响,这些电力由内质网的膜电位以及Ca2+通量改变该电位的难易程度(即内质网膜的电阻)等因素决定。尽管这些电力无疑在塑造内质网Ca2+动态中起着基本作用,但目前关于内质网膜生物物理特性的直接实验信息非常少。对内质网腔内Ca2+如何调节的进一步研究,最好通过直接测量来进行,对于理解Ca2+如何协调细胞功能至关重要。在已知胞质Ca2+浓度的条件下直接监测内质网Ca2+,也可能有助于获取关于内质网难以捉摸的生物物理信息,比如内质网膜两侧的电位差。

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