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过氧化氢和紫外线A辐射诱导的遗传毒性应激后角质形成细胞中G2/M检查点激活的差异。

Differences in activation of G2/M checkpoint in keratinocytes after genotoxic stress induced by hydrogen peroxide and ultraviolet A radiation.

作者信息

Thorn T, Gniadecki R, Petersen A B, Vicanova J, Wulf H C

机构信息

Department of Dermatology, Bispebjerg Hospital, University of Copenhagen, Denmark.

出版信息

Free Radic Res. 2001 Oct;35(4):405-16. doi: 10.1080/10715760100300921.

Abstract

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.

摘要

长波紫外线辐射(UVA)可通过活性氧(ROS)导致广泛的DNA损伤。在本研究中,我们检测了UVA和H2O2介导的DNA损伤对转化的角质形成细胞系HaCaT中G2/M期检查点的诱导及细胞周期进程是否具有相同的影响。通过采用单细胞凝胶电泳(彗星试验),我们确定了UVA和H2O2在诱导碱不稳定位点(氧化DNA降解的一个指标)方面的等效剂量。然而,与处理后24小时导致明显的G2/M期细胞周期停滞的H2O2不同,UVA照射不影响细胞周期进程。将UVA剂量增加至150 kJ/m2并不影响细胞周期和增殖,而增加H2O2浓度则导致细胞周期阻滞或细胞死亡。细胞计量分析显示,G2/M期细胞周期停滞发生在细胞周期蛋白B1限制点之后。我们得出结论,UVA诱导的DNA损伤易于修复且不干扰细胞生长,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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