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首页> 外文期刊>Journal of cellular biochemistry. >Deregulation of cyclin-dependent kinase 2 activity correlates with UVC-induced apoptosis in Chinese hamster ovary cells.
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Deregulation of cyclin-dependent kinase 2 activity correlates with UVC-induced apoptosis in Chinese hamster ovary cells.

机译:细胞周期蛋白依赖性激酶2活性的失调与UVC诱导的中国仓鼠卵巢细胞凋亡有关。

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摘要

Progression through the cell cycle relies on the activities of cyclin-dependent kinases (Cdk), which in turn are modulated by inhibitory proteins such as p21(waf1/cip1) that are induced when genomic damage occurs. In this study, we show that exposure of normal mammalian cells, such as NIH3T3 fibroblasts, to UVC (25 J/m2, at 254 nm) induces the expression of p21 without causing significant apoptosis, whereas similar treatment of Chinese hamster ovary (CHO-K1) cells with UVC causes apoptosis without inducing p21. The absence of p21 in UV-irradiated CHO-K1 cells is accompanied by the deregulation of Cdk2 activity. The elevation of Cdk2 activity correlates with the increase of UV-induced apoptosis, which can be suppressed by small-molecule Cdk2 inhibitors such as roscovitine and pyrrolidine dithiocarbamate. The results of this study suggest that the deregulation of Cdk2 activity may be critical to UV-induced apoptosis in CHO-K1 cells.
机译:整个细胞周期的进展取决于细胞周期蛋白依赖性激酶(Cdk)的活性,而这些蛋白又会受到抑制性蛋白质(如p21(waf1 / cip1))的调节,而这些蛋白质在发生基因组损伤时会被诱导。在这项研究中,我们显示正常哺乳动物细胞(如NIH3T3成纤维细胞)暴露于UVC(25 J / m2,在254 nm下)可诱导p21的表达而不会引起明显的细胞凋亡,而对中国仓鼠卵巢(CHO-具有UVC的K1)细胞可导致细胞凋亡而不诱导p21。在紫外线照射的CHO-K1细胞中不存在p21,伴随着Cdk2活性的失控。 Cdk2活性的升高与紫外线诱导的细胞凋亡的增加有关,这可以被小分子Cdk2抑制剂(如roscovitine和吡咯烷二硫代氨基甲酸酯)抑制。这项研究的结果表明,Cdk2活性的失控可能是紫外线诱导CHO-K1细胞凋亡的关键。

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