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细胞周期中钙库操纵性钙内流的调控。

Regulation of store-operated Ca2+ entry during the cell cycle.

机构信息

Department of Physiology and Biophysics, Weill Cornell Medical College in Qatar (WCMC-Q), Education City, Qatar Foundation, Doha, Qatar.

出版信息

J Cell Sci. 2010 Jul 1;123(Pt 13):2155-62. doi: 10.1242/jcs.069690.

Abstract

Cytoplasmic Ca(2+) signals are central to numerous cell physiological processes, including cellular proliferation. Historically, much of the research effort in this area has focused on the role of Ca(2+) signals in cell-cycle progression. It is becoming clear, however, that the relationship between Ca(2+) signaling and the cell cycle is a 'two-way street'. Specifically, Ca(2+)-signaling pathways are remodeled during M phase, leading to altered Ca(2+) dynamics. Such remodeling probably better serves the large variety of functions that cells must perform during cell division compared with during interphase. This is clearly the case during oocyte meiosis, because remodeling of Ca(2+) signals partially defines the competence of the egg to activate at fertilization. Store-operated Ca(2+) entry (SOCE) is a ubiquitous Ca(2+)-signaling pathway that is regulated during M phase. In this Commentary, we discuss the latest advances in our understanding of how SOCE is regulated during cell division.

摘要

细胞质 Ca(2+)信号是许多细胞生理过程的核心,包括细胞增殖。历史上,该领域的大部分研究都集中在 Ca(2+)信号在细胞周期进程中的作用。然而,越来越明显的是,Ca(2+)信号与细胞周期之间的关系是“双向的”。具体来说,Ca(2+)信号通路在 M 期发生重构,导致 Ca(2+)动力学发生改变。与细胞分裂间期相比,这种重构可能更适合细胞在细胞分裂过程中必须执行的各种功能。这在卵母细胞减数分裂中显然是如此,因为 Ca(2+)信号的重构部分定义了卵子在受精时激活的能力。储存操作的 Ca(2+)内流(SOCE)是一种普遍存在的 Ca(2+)信号通路,在 M 期受到调节。在这篇评论中,我们讨论了我们对 SOCE 在细胞分裂过程中如何受到调节的最新理解进展。

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