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Quantitative characteristics of clustered DNA damage in irradiated cells by heavy ion beams

机译:重离子束辐照细胞中聚集的DNA损伤的定量特征

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摘要

Heavy ion beam as typical high linear energy transfer (LET) radiation produces more expanding ionization domain around their tracks than low LET radiation such as X-rays and gamma rays. Thus, heavy ion beam can cause more densely accumulated damage cluster in the target DNA, termed clustered DNA damage. This damage exhibits difficulty for repair and inhibition of DNA replication with its complex structure [ ]. So, clustered DNA damage is thought to be strongly involved in the biological effectiveness of heavy ion beam. However, a lot of studies have presented no certain correlation between yields of clustered DNA damage and severity of radiation effect. We previously indicated that the yields of clustered DNA damage decreased with increasing LET in the DNA molecules irradiated in test tubes with gamma rays, and carbon and iron ion beams whose showed different LET, respectively [ ]. In this study, we aimed to reveal correlation between clustered DNA damage and the LET of heavy ion beam in the irradiated cells.In the experiments, Chinese hamster ovary AA8 cells growing exponentially were irradiated by carbon, silicon, argon and iron ion beams from Heavy Ion Medical Accelerator in Chiba (HIMAC) of the National Institute of Radiological Sciences, Japan. These LETs were 13, 55, 90 and 200 keV/µm, respectively. For comparison, we used gamma rays from 137Cs-gamma source, Gammacell 40 (Atomic Energy of Canada Ltd), at Saga University. The irradiated cells were subjected by static-field gel electrophoresis to quantify clustered DNA damage of the genomic DNA. For this analysis, we used Fpg and endonuclease III for clustered DNA damage including oxidative purine and pyrimidine lesions, respectively. We also analysed the corresponding isolated DNA damages by aldehyde reactive probe method [ ], and the surviving fractions of the irradiated cells in this study.The electrophoretic results indicated that total yields of clustered DNA damage in the irradiated cells decreased with increasing LET, including the double-strand break (DSB) and the respective clustered base damages (Fig. ). This result conforms to our previous study with the irradiated DNA molecules [ ]. The damage kinetics is thought to be mainly derived from two reasons: decreasing fluxes and increasing reaction with reactive oxygen species each other in increase in LET. In the clustered DNA damage induced by each radiation, the most decremental fraction was clustered base damage, but not DSB. The isolated DNA damages decreased with increasing LET like clustered DNA damage in this study (data not shown). These results make us realize the degree of contribution of direct and indirect effects of ionizing radiation. The certain amount of DSB were derived from the direct effect and showed less reactivity to LET. In contrast, oxidative base lesions were mainly generated by indirect effect with reactive oxygen species, which sensitively responded to LET change. We also found seemingly conflicted result of the relationship between LET and RBE (data not shown). We need further study to elucidate act of clustered DNA damage in radiobiological effect with heavy ion beams. The yields of clustered DNA damages in the cells irradiated with respective ionizing radiations. Each clustered DNA damage consists of DSB (open bar) and clustered base damage (closed bar), and calculated from the strength of released band on electrophoretic gel.
机译:重离子束作为典型的高线性能量转移(LET)辐射,与低LET辐射(例如X射线和伽玛射线)相比,在其轨迹周围产生更多的扩展电离域。因此,重离子束会在目标DNA中引起更密集的损伤簇,称为簇DNA损伤。这种损伤表现出修复和抑制具有复杂结构的DNA复制的困难[]。因此,人们认为簇状DNA损伤与重离子束的生物学有效性密切相关。但是,许多研究表明,簇状DNA损伤的产生与辐射效应的严重性之间没有确定的相关性。我们以前曾指出,簇状DNA损伤的产生率随在伽玛射线,分别显示不同LET的碳和铁离子束辐照的试管中照射的DNA分子中LET的增加而降低[]。本研究旨在揭示成簇的DNA损伤与被辐射细胞中重离子束LET的相关性。在实验中,来自中国重金属的碳,硅,氩和铁离子束辐射了成倍生长的中国仓鼠卵巢AA8细胞。日本国立放射科学研究所千叶县离子医疗促进剂(HIMAC)。这些LETs分别为13、55、90和200 keV / µm。为了进行比较,我们使用了佐贺大学的 137 Cs-伽玛射线源,即加拿大原子能有限公司的Gammacell 40(伽马电池40)。用静态场凝胶电泳对被照射的细胞进行定量,以量化基因组DNA的簇状DNA损伤。对于此分析,我们使用Fpg和核酸内切酶III分别对簇状DNA损伤,包括氧化嘌呤和嘧啶损伤。我们还通过醛反应探针法[]分析了相应的分离的DNA损伤,以及本研究中被辐照细胞的存活分数。电泳结果表明,随着LET的增加,辐照细胞中簇状DNA损伤的总产量降低,包括双链断裂(DSB)和各自的簇状基础破坏(图)。此结果与我们先前对辐照的DNA分子的研究一致[]。破坏动力学被认为主要来自两个原因:通量的减少和LET中与活性氧的反应增加。在每次辐射诱导的簇状DNA损伤中,减少最多的部分是簇状碱基损伤,而不是DSB。在这项研究中,分离的DNA损伤随着LET的增加而降低,就像簇状DNA损伤一样(数据未显示)。这些结果使我们认识到电离辐射的直接和间接作用的贡献程度。一定量的DSB源自直接作用,并且显示出对LET的反应性较低。相反,氧化性基础病变主要是由活性氧的间接作用产生的,活性氧对LET的变化敏感。我们还发现LET和RBE之间的关系看似矛盾的结果(数据未显示)。我们需要进一步研究,以阐明簇状DNA损伤在重离子束的放射生物学效应中的作用。 <!-fig ft0-> <!-fig mode = art f1-> <!-caption a7->分别用电离辐射照射的细胞中簇状DNA损伤的产生。每个簇状DNA损伤均由DSB(空心柱)和簇状碱基损伤(实心柱)组成,并根据电泳凝胶上释放带的强度计算得出。

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