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重离子辐照后CHO细胞中DNA双链断裂的诱导与修复

Induction and rejoining of DNA double-strand breaks in CHO cells after heavy ion irradiation.

作者信息

Taucher-Scholz G, Heilmann J, Kraft G

机构信息

Gesellschaft für Schwerionenforschung, Darmstadt, Germany.

出版信息

Adv Space Res. 1996;18(1-2):83-92. doi: 10.1016/0273-1177(95)00794-f.

Abstract

DNA double-strand breaks (DSBs) are the crucial events ultimately leading to cell inactivation. Aimed at understanding the biological action of the charged particle component of cosmic radiation, the induction of DSBs and their repairability was evaluated in Chinese hamster ovary (CHO-K1) cells after exposure to accelerated particles. Irradiations were performed with various ion species including O, Ni and Ca, covering a LET range from 20 to 2000 keV/micrometer. DSBs were determined for plateau-phase cells using the electrophoretic elution of radiation-induced DNA fragments in a static electric field combined with fluorescence scanning of ethidium bromide stained gels. Assuming a DSB yield of 22 DSB per Gy per cell, as derived from X-irradiation, cross-sections for DSB production were calculated from the corresponding fluence-effect curves at a fraction of 0.7 of DNA retained. The same ordinate was used as a reference for the calculation of relative biological efficiency (RBE) for DSB induction. At low LETs (< or = 20 keV/micrometer) RBE values slightly above unity were obtained, but a decrease of RBE was observed with increasing LET. In the region of 100-200 keV/micrometer the RBE for initial DSB induction was clearly below unity. Rejoining of DSBs was assessed by measuring the fraction of DNA retained following post-irradiation incubation of cells under culture conditions. After exposure to Ca ions, DSB rejoining was considerably impaired compared to X-rays.

摘要

DNA双链断裂(DSB)是最终导致细胞失活的关键事件。为了了解宇宙辐射带电粒子成分的生物学作用,在加速粒子照射后,对中国仓鼠卵巢(CHO-K1)细胞中DSB的诱导及其可修复性进行了评估。使用包括氧、镍和钙在内的各种离子种类进行照射,LET范围为20至2000keV/微米。对于处于平台期的细胞,通过在静电场中对辐射诱导的DNA片段进行电泳洗脱并结合溴化乙锭染色凝胶的荧光扫描来测定DSB。假设从X射线照射得出的DSB产率为每细胞每戈瑞22个DSB,根据保留0.7比例的DNA时相应的注量-效应曲线计算DSB产生的截面。相同的纵坐标用作计算DSB诱导相对生物效应(RBE)的参考。在低LET(≤20keV/微米)时获得略高于1的RBE值,但随着LET增加观察到RBE降低。在100 - 200keV/微米区域,初始DSB诱导的RBE明显低于1。通过测量细胞在培养条件下照射后孵育后保留的DNA比例来评估DSB的重新连接。与X射线相比,暴露于钙离子后,DSB的重新连接受到显著损害。

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