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分析8-羟基脱氧鸟苷5'-单磷酸(8-OH-dGMP)作为γ射线照射后细胞氧化性DNA损伤的可靠标志物。

Analysis of 8-hydroxydeoxyguanosine 5'-monophosphate (8-OH-dGMP) as a reliable marker of cellular oxidative DNA damage after gamma-irradiation.

作者信息

Mei Nan, Tamae Kazuyoshi, Kunugita Naoki, Hirano Takeshi, Kasai Hiroshi

机构信息

Department of Environmental Oncology, Institute of Industrial Ecological Sciences, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

Environ Mol Mutagen. 2003;41(5):332-8. doi: 10.1002/em.10165.

Abstract

In order to improve 8-hydroxyguanine (8-OH-Gua) detection in DNA, we digested isolated DNA with nuclease P1 and analyzed for 8-hydroxydeoxyguanosine 5'-monophosphate (8-OH-dGMP) using a high-performance liquid chromatography system equipped with an electrochemical detector (HPLC-ECD). The amount of 8-OH-Gua in the DNA was expressed as the ratio of 8-OH-dGMP to deoxycytidine monophosphate (dCMP). Using this analysis, the background level of 8-OH-Gua in DNA from human lung carcinoma cells (A549) was several-fold lower than that obtained by a previous method. A549 cells were exposed to 20-60 Gy of gamma-radiation and an increase in 8-OH-Gua concentration was observed with increasing gamma-ray dose (0.3 residues per 10(7) dCMP per Gy). Moreover, by an immunohistochemical procedure using a commercial FITC-kit, 8-OH-Gua was clearly detected in A549 cells and the fluorescence intensity of cells with oxidative DNA damage increased with the doses of gamma-irradiation. Using an endonuclease nicking assay, we also found that gamma-rays decreased 8-OH-Gua repair activity. The results indicate that 8-OH-dGMP is a useful and sensitive marker for estimating oxidative damage in DNA.

摘要

为了改进DNA中8-羟基鸟嘌呤(8-OH-Gua)的检测方法,我们用核酸酶P1消化分离的DNA,并使用配备电化学检测器的高效液相色谱系统(HPLC-ECD)分析8-羟基脱氧鸟苷5'-单磷酸(8-OH-dGMP)。DNA中8-OH-Gua的含量以8-OH-dGMP与脱氧胞苷单磷酸(dCMP)的比值表示。通过这种分析方法,人肺癌细胞(A549)DNA中8-OH-Gua的背景水平比之前的方法低几倍。将A549细胞暴露于20-60 Gy的γ射线辐射下,观察到随着γ射线剂量增加,8-OH-Gua浓度升高(每Gy每10(7) dCMP中有0.3个残基)。此外,通过使用商业FITC试剂盒的免疫组织化学方法,在A549细胞中清晰检测到8-OH-Gua,并且具有氧化性DNA损伤的细胞的荧光强度随着γ射线辐射剂量增加而增强。使用内切酶切口试验,我们还发现γ射线降低了8-OH-Gua的修复活性。结果表明,8-OH-dGMP是评估DNA氧化损伤的一种有用且灵敏的标志物。

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