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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Hypothermia postpones DNA damage repair in irradiated cells and protects against cell killing.
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Hypothermia postpones DNA damage repair in irradiated cells and protects against cell killing.

机译:体温过低会延迟照射细胞的DNA损伤修复,并防止细胞杀伤。

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摘要

Hibernation is an established strategy used by some homeothermic organisms to survive cold environments. In true hibernation, the core body temperature of an animal may drop to below 0 degrees C and metabolic activity almost cease. The phenomenon of hibernation in humans is receiving renewed interest since several cases of victims exhibiting core body temperatures as low as 13.7 degrees C have been revived with minimal lasting deficits. In addition, local cooling during radiotherapy has resulted in normal tissue protection. The experiments described in this paper were prompted by the results of a very limited pilot study, which showed a suppressed DNA repair response of mouse lymphocytes collected from animals subjected to 7-Gy total body irradiation under hypothermic (13 degrees C) conditions, compared to normothermic controls. Here we report that human BJ-hTERT cells exhibited a pronounced radioprotective effect on clonogenic survival when cooled to 13 degrees C during and 12h after irradiation. Mild hypothermia at 20 and 30 degrees C also resulted in some radioprotection. The neutral comet assay revealed an apparent lack on double strand break (DSB) rejoining at 13 degrees C. Extension of the mouse lymphocyte study to ex vivo-irradiated human lymphocytes confirmed lower levels of induced phosphorylated H2AX (gamma-H2AX) and persistence of the lesions at hypothermia compared to the normal temperature. Parallel studies of radiation-induced oxidatively clustered DNA lesions (OCDLs) revealed partial repair at 13 degrees C compared to the rapid repair at 37 degrees C. For both gamma-H2AX foci and OCDLs, the return of lymphocytes to 37 degrees C resulted in the resumption of normal repair kinetics. These results, as well as observations made by others and reviewed in this study, have implications for understanding the radiobiology and protective mechanisms underlying hypothermia and potential opportunities for exploitation in terms of protecting normal tissues against radiation.
机译:休眠是一些恒温生物在寒冷环境中生存所采用的既定策略。在真正的冬眠状态下,动物的核心体温可能会降至0摄氏度以下,并且代谢活动几乎停止。人类的冬眠现象引起了人们的新兴趣,因为几例显示核心体温低至13.7摄氏度的受害者得以复活,且持续时间极短。此外,放疗期间的局部冷却还可以保护组织正常。本文所描述的实验是由一项非常有限的先导研究的结果所推动的,该研究表明,与在低温(13摄氏度)条件下进行7-Gy全身辐照的动物相比,小鼠淋巴细胞的DNA修复反应受到抑制。正常体温控制。在这里,我们报道人类BJ-hTERT细胞在放疗期间和放疗后12h冷却到13摄氏度时,对克隆形成存活表现出明显的放射防护作用。在20和30摄氏度的低温下也能产生一定的辐射防护作用。中性彗星试验显示在13°C下重新结合的双链断裂(DSB)明显缺乏。将小鼠淋巴细胞研究扩展至离体辐射的人淋巴细胞,证实了较低水平的诱导的磷酸化H2AX(γ-H2AX)和其持久性低温下皮损与正常温度相比。辐射诱导的氧化簇DNA损伤(OCDLs)的并行研究表明,与37°C时的快速修复相比,在13°C时可进行部分修复。对于γ-H2AX灶和OCDL,淋巴细胞恢复到37°C导致恢复正常的修复动力学。这些结果,以及其他人的观察结果以及本研究中进行的评论,都对理解体温过低的放射生物学和保护机制以及在保护正常组织免受辐射方面的潜在开发机会具有启示。

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