x射线辐照人成纤维细胞中γ - h2ax、53BP1、pATM和p-p53 (Ser-15)残余灶的剂量阈值

Andrey Osipov, Anna Chigasova, Oleg Belov, Elizaveta Yashkina, Maxim Ignatov, Yuriy Fedotov, Natalia Vorobyeva, Andreyan N Osipov
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摘要

背景:在暴露于电离辐射(IR)后24小时或更长时间内,残余DNA修复点的计数常用于评估DNA双链断裂修复的效率。然而,辐照细胞中残余病灶的数量与辐照剂量之间的关系仍然知之甚少。本研究的目的是研究在0.1 ~ 5gy吸收剂量范围内的x射线照射对正常人成纤维细胞中残余DNA修复病灶的剂量反应。材料和方法:用x射线照射成纤维细胞,吸收剂量率为0.2 Gy/min。辐照后的细胞孵育0.5、24、48和72 h。免疫荧光可视化γ - h2ax、53BP1、pATM和p-p53 (Ser-15)病灶采用DARFI软件和人工评分法进行枚举。此外,还进行了克隆生存分析。结果:用曲棍球棒模型进行的数据分析显示,在所研究的所有蛋白质的残留病灶存在剂量阈值。估计的阈值剂量接近细胞存活曲线计算的准阈值剂量(Dq = 0.99±0.09 Gy)。结论:在辐照成纤维细胞中,阈值剂量和Dq的计算值非常吻合,证明残留病灶是细胞仍在试图修复潜在致命DNA损伤的部位。
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Dose threshold for residual γH2AX, 53BP1, pATM and p-p53 (Ser-15) foci in X-ray irradiated human fibroblasts.

Background: Enumeration of residual DNA repair foci 24 hours or more after exposure to ionizing radiation (IR) is often used to assess the efficiency of DNA double-strand break repair. However, the relationship between the number of residual foci in irradiated cells and the radiation dose is still poorly understood. The aim of this work was to investigate the dose responses for residual DNA repair foci in normal human fibroblasts after X-ray exposure in the absorbed dose range from 0.1 to 5 Gy.

Materials and methods: Fibroblasts were irradiated using a X-ray unit at an absorbed dose rate of 0.2 Gy/min. Irradiated cells were incubated for 0.5, 24, 48 and 72 h. Immunofluorescence visualized γH2AX, 53BP1, pATM and p-p53 (Ser-15) foci were enumerated using DARFI software and by manual scoring. Additionally, clonogenic survival analysis was performed.

Results: The data analysis performed with the hockey stick model showed the presence of a dose threshold for the residual foci of all proteins studied. The estimated threshold doses are close to the quasi-threshold dose (Dq = 0.99 ± 0.09 Gy) calculated from the cell survival curve.

Conclusion: The excellent agreement between the calculated values of the threshold dose and Dq in irradiated fibroblasts proves that residual foci are sites, where cells are still attempting to repair potentially lethal DNA damage.

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