首页> 外文期刊>Free radical research >Differences in activation of G2/M checkpoint in keratinocytes after genotoxic stress induced by hydrogen peroxide and ultraviolet A radiation.
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Differences in activation of G2/M checkpoint in keratinocytes after genotoxic stress induced by hydrogen peroxide and ultraviolet A radiation.

机译:过氧化氢和紫外线A辐射引起的基因毒性应激后,角质形成细胞中G2 / M检查点激活的差异。

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Long-wave ultraviolet radiation (UVA) may cause extensive DNA damage via reactive oxygen species (ROS). In this study we examined whether UVA- and H2O2-mediated DNA damage have equivalent effects on the induction of G2/M phase checkpoint and cell cycle progression in a transformed keratinocyte cell line HaCaT. By employing single cell gel electrophoresis (comet assay) we determined the equipotent doses of UVA and H2O2 with respect to the induction of alkali-labile sites (an indicator of oxidative DNA decay). However, in contrast to H2O2 which caused a pronounced G2/M cell cycle arrest 24 h after treatment, UVA irradiation did not affect cell cycle progression. Increasing UVA doses up to 150 kJ/m2 did not affect cell cycle and proliferation whereas increasing H2O2 concentrations caused a cell cycle block or cell death. Cytometric analysis revealed that G2/M cell cycle arrest took place beyond the cyclin B1 restriction point. We conclude that the DNA damage induced by UVA is easily repaired and does not perturb cell growth, whereas the H2O2-induced damage leads ultimately to cell cycle arrest or cell death.
机译:长波紫外线辐射(UVA)可能会通过活性氧(ROS)引起广泛的DNA损伤。在这项研究中,我们检查了UVA和H2O2介导的DNA损伤在转化的角质形成细胞系HaCaT中对G2 / M期检查点的诱导和细胞周期进程是否具有同等作用。通过采用单细胞凝胶电泳(彗星试验),我们确定了对碱不稳定位点(氧化性DNA降解的指示剂)的诱导,UVA和H2O2的等效剂量。但是,与H2O2在处理后24小时引起明显的G2 / M细胞周期停滞相比,UVA辐照不会影响细胞周期进程。增加至150 kJ / m2的UVA剂量不会影响细胞周期和增殖,而增加的H2O2浓度则导致细胞周期阻滞或细胞死亡。细胞计数分析表明,G2 / M细胞周期停滞发生在细胞周期蛋白B1限制点之外。我们得出的结论是,UVA诱导的DNA损伤易于修复,不会干扰细胞生长,而H2O2诱导的损伤最终导致细胞周期停滞或细胞死亡。

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