Ca2+ signaling, genes and the cell cycle

被引:44
|
作者
Machaca, Khaled [1 ]
机构
[1] Educ City Qatar Fdn, Dept Physiol & Biophys, WCMC Q, Doha, Qatar
关键词
Cell cycle; Ca signaling; Gene expression; Fertilization; T-cell activation; GERMINAL VESICLE BREAKDOWN; SEA-URCHIN EGGS; MATURATION-PROMOTING FACTOR; XENOPUS-LAEVIS OOCYTES; NUCLEAR-ENVELOPE BREAKDOWN; INTRACELLULAR CALCIUM; MEIOTIC MATURATION; ENDOPLASMIC-RETICULUM; DEPENDENT REGULATION; METAPHASE ARREST;
D O I
10.1016/j.ceca.2010.10.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Changes in the concentration and spatial distribution of Ca2+ ions in the cytoplasm constitute a ubiquitous intracellular signaling module in cellular physiology. With the advent of Ca2+ dyes that allow direct visualization of Ca2+ transients, combined with powerful experimental tools such as electrophysiological recordings, intracellular Ca2+ transients have been implicated in practically every aspect of cellular physiology, including cellular proliferation. Ca2+ signals are associated with different phases of the cell cycle and interfering with Ca2+ signaling or downstream pathways often disrupts progression of the cell cycle. Although there exists a dependence between Ca2+ signals and the cell cycle the mechanisms involved are not well defined and given the cross-talk between Ca2+ and other signaling modules, it is difficult to assess the exact role of Ca2+ signals in cell cycle progression. Two exceptions however, include fertilization and T-cell activation, where well-defined roles for Ca2+ signals in mediating progression through specific stages of the cell cycle have been clearly established. In the case of T-cell activation Ca2+ regulates entry into the cell cycle through the induction of gene transcription. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:243 / 250
页数:8
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