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通过质膜钙库操纵型钙通道的钙离子内流与内质网钙离子泵的特权偶联。

Privileged coupling between Ca(2+) entry through plasma membrane store-operated Ca(2+) channels and the endoplasmic reticulum Ca(2+) pump.

机构信息

Instituto de Biología y Genética Molecular, Universidad de Valladolid y Consejo Superior de Investigaciones Científicas, c/ Sanz y Forés s/n, 47003 Valladolid, Spain.

出版信息

Mol Cell Endocrinol. 2012 Apr 28;353(1-2):37-44. doi: 10.1016/j.mce.2011.08.021. Epub 2011 Aug 24.

Abstract

The sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) is the third element of capacitative calcium entry. It colocalizes with STIM1 and Orai1 at puncta, where couples plasma membrane store-operated Ca(2+) channels (SOC) to Ca(2+) pumping into the ER. The efficiency of this calcium entry-calcium refilling (CECR) coupling is comparable to the classic excitation-response transduction mechanisms. This allows efficient filling of the endoplasmic reticulum (ER) with the Ca(2+) entering through SOC channels with little progression of the Ca(2+) wave towards the cell core. CECR coupling is very sensitive to changes in stoichiometry among STIM, Orai and SERCA, with excess Orai antagonizing ER refilling. ER takes up most of the calcium load that enters through SOC, whereas mitochondria take up a very small fraction. This difference is due to the spatial positioning with regard to SOC, the amplitude of the high Ca(2+) microdomains, and the differences in the Ca(2+) affinity of the uptake mechanisms.

摘要

肌浆/内质网 Ca(2+) -ATP 酶(SERCA)是电容钙内流的第三个组成部分。它与 STIM1 和 Orai1 在质膜上的点状结构中共定位,在这里,质膜储存操作 Ca(2+) 通道(SOC)与 Ca(2+)泵入内质网耦联。这种钙内流-钙再填充(CECR)偶联的效率与经典的兴奋-反应转导机制相当。这使得 SOC 通道进入内质网的 Ca(2+) 能够有效地填充,而 Ca(2+) 波向细胞核心的推进很少。CECR 偶联对 STIM、Orai 和 SERCA 之间的计量比变化非常敏感,过量的 Orai 拮抗内质网再填充。内质网吸收了通过 SOC 进入的大部分钙负荷,而线粒体只吸收了很小的一部分。这种差异归因于 SOC 的空间定位、高 Ca(2+) 微区的幅度以及摄取机制的 Ca(2+) 亲和力的差异。

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