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The Mammalian Circadian Clock Gene Per2 Modulates Cell Death in Response to Oxidative Stress

机译:哺乳动物的昼夜节律时钟基因Per2调节细胞死亡对氧化应激的响应。

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摘要

Living in the earth’s oxygenated environment forced organisms to develop strategies to cope with the damaging effects of molecular oxygen known as reactive oxygen species (ROS). Here, we show that Per2, a molecular component of the mammalian circadian clock, is involved in regulating a cell’s response to oxidative stress. Mouse embryonic fibroblasts (MEFs) containing a mutation in the Per2 gene are more resistant to cytotoxic effects mediated by ROS than wild-type cells, which is paralleled by an altered regulation of bcl-2 expression in Per2 mutant MEFs. The elevated survival rate and alteration of NADH/NAD+ ratio in the mutant cells is reversed by introduction of the wild-type Per2 gene. Interestingly, clock synchronized cells display a time dependent sensitivity to paraquat, a ROS inducing agent. Our observations indicate that the circadian clock is involved in regulating the fate of a cell to survive or to die in response to oxidative stress, which could have implications for cancer development and the aging process.
机译:生活在地球上充满氧气的环境中,迫使生物体制定策略来应对分子氧(活性氧)的破坏作用。在这里,我们证明了Per2是哺乳动物生物钟的分子成分,参与调节细胞对氧化应激的反应。与野生型细胞相比,在Per2基因中包含突变的小鼠胚胎成纤维细胞(MEF)对ROS介导的细胞毒性作用具有更强的抵抗力,这与在Per2突变MEF中bcl-2表达的调控改变相平行。通过导入野生型Per2基因可以逆转突变细胞中存活率的升高和NADH / NAD + 比的改变。有趣的是,时钟同步单元显示出对百草枯(一种ROS诱导剂)的时间依赖性。我们的观察结果表明,昼夜节律时钟参与调节细胞的命运,以应对氧化应激而存活或死亡,这可能对癌症的发展和衰老过程有影响。

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