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首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Evidence for the involvement of DNA-dependent protein kinase in the phenomena of low dose hyper-radiosensitivity and increased radioresistance.
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Evidence for the involvement of DNA-dependent protein kinase in the phenomena of low dose hyper-radiosensitivity and increased radioresistance.

机译:DNA依赖蛋白激酶参与低剂量超放射敏感性和放射抵抗力增加现象的证据。

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Purpose: To investigate the role of DNA-dependent protein kinase (DNA-PK) in the phenomena of low dose hyper-radiosensitivity (HRS) and increased radioresistance (IRR) using the genetically related M059 cell lines of disparate PRKDC status. Materials and methods: Clonogenic survival was measured for the three cell lines following low doses of X-irradiation using a flowactivated cell sorting (FACS) plating technique. The presence of PRKDC, G22p1 and Xrcc5 proteins was determined by Western blotting and a kinase assay used to measure DNA-PK complex activity. Results: The survival responses for the three cell lines over the 0-0.3Gy dose range were comparable, but differences in radiosensitivity were evident at doses >0.4Gy. M059K and M059J/Fus1 cells (both PRKDC competent) exhibited marked HRS/IRR responses, albeit to different extents. M059J cells (PRKDC incompetent) were extremely radiosensitive exhibiting a linear survival curve with no evidence of IRR. The presence of IRR was coincident with the presence of PRKDC protein and functional DNA-PK activity. Conclusions: HRS is a response that is independent of DNA-PK activity. In contrast, IRR showed a dependence on the presence of PRKDC protein and functional DNA-PK activity. These data support a role for DNA-PK activity in the IRR response.
机译:目的:使用与遗传相关的不同PRKDC状态的M059细胞系,研究DNA依赖性蛋白激酶(DNA-PK)在低剂量超放射敏感性(HRS)和放射抗性(IRR)现象中的作用。材料和方法:使用流激活细胞分选(FACS)铺板技术,在低剂量X射线照射后测量了三种细胞系的克隆存活率。通过蛋白质印迹和用于测定DNA-PK复合物活性的激酶测定法确定PRKDC,G22p1和Xrcc5蛋白的存在。结果:三种细胞系在0-0.3Gy剂量范围内的存活反应具有可比性,但在> 0.4Gy剂量下,放射敏感性存在明显差异。 M059K和M059J / Fus1细胞(均符合PRKDC)显示出明显的HRS / IRR反应,尽管程度不同。 M059J细胞(PRKDC不适合)对放射线极为敏感,显示出线性存活曲线,没有IRR的证据。 IRR的存在与PRKDC蛋白和功能性DNA-PK活性的存在相吻合。结论:HRS是一种独立于DNA-PK活性的反应。相反,IRR显示对PRKDC蛋白的存在和功能性DNA-PK活性的依赖性。这些数据支持了DNA-PK活性在IRR反应中的作用。

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