Intraluminal calcium as a primary regulator of endoplasmic reticulum function

被引:180
作者
Burdakov, D
Petersen, OH
Verkhratsky, A
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
[2] Univ Liverpool, Physiol Lab, MRC Grp, Liverpool L69 3BX, Merseyside, England
基金
英国惠康基金;
关键词
endoplasmic reticulum; calcium; signalling; SERCA; neurodegeneration;
D O I
10.1016/j.ceca.2005.06.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The concentration of Ca(2+) inside the lumen of endoplasmic reticulum (ER) regulates a vast array of spatiotemporally distinct cellular processes, from intracellular Ca(2+) signals to intra-ER protein processing and cell death. This review summarises recent data on the mechanisms of luminal Ca(2+)-dependent regulation of Ca(2+) 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 Ca(2+) fluxes are subject to basic electrical forces, determined by factors such as the membrane potential of the ER and the ease with which Ca(2+) 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 [Ca(2+)](ER) dynamics, at present there is very little direct experimental information about the biophysical properties of the ER membrane. Further studies of how intraluminal [Ca(2+)] is regulated, best carried out with direct measurements, are vital for understanding how Ca(2+) orchestrates cell function. Direct monitoring of [Ca(2+)](ER) under conditions where the cytosolic [Ca(2+)] is known may also help to capture elusive biophysical information about the ER, such as the potential difference across the ER membrane. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:303 / 310
页数:8
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