共 144 条
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.
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页码:243 / 250
页数:8
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