Hypothermia postpones DNA damage repair in irradiated cells and protects against cell killing

被引:28
作者
Baird, Brandon J. [1 ]
Dickey, Jennifer S. [1 ]
Nakamura, Asako J. [1 ]
Redon, Christophe E. [1 ]
Parekh, Palak [1 ]
Griko, Yuri V. [3 ]
Aziz, Khaled [2 ]
Georgakilas, Alexandros G. [2 ]
Bonner, William M. [1 ]
Martin, Olga A. [1 ]
机构
[1] NCI, Mol Pharmacol Lab, CCR, Bethesda, MD 20892 USA
[2] E Carolina Univ, Dept Biol, Greenville, NC 27858 USA
[3] NASA, Ames Res Ctr, Radiat & Space Biotechnol Branch, Moffett Field, CA 94035 USA
基金
美国国家卫生研究院;
关键词
Hypothermia; Radioprotective effect; Cell survival; DNA damage; DOUBLE-STRAND BREAKS; BASE EXCISION-REPAIR; INDUCED HAIR LOSS; IONIZING-RADIATION; GROUND-SQUIRRELS; BLOOD-LYMPHOCYTES; TOPOISOMERASE-I; BRAIN NEURONS; CHEMOTHERAPY; TEMPERATURE;
D O I
10.1016/j.mrfmmm.2010.12.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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 (0CDL5) 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. (C) 2011 Published by Elsevier B.V.
引用
收藏
页码:142 / 149
页数:8
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