Radiation-induced double strand breaks and subsequent apoptotic DNA fragmentation in human peripheral blood mononuclear cells

被引:29
作者
Ghardi, Myriam [1 ]
Moreels, Marjan [1 ]
Chatelain, Bernard [2 ]
Chatelain, Christian [2 ]
Baatout, Sarah [1 ]
机构
[1] CEN SCK, Belgian Nucl Res Ctr, Radlobiol Unit, B-2400 Mol, Belgium
[2] UCL Mt Godinne Univ Hosp, Lab Expt Hematol & Oncol, B-5530 Yvoir, Belgium
关键词
DNA damage; DNA repair; DSB repair kinetics; apoptosis; gamma H2AX; biodosimetry; ionizing radiation; HISTONE H2AX PHOSPHORYLATION; LOW-DOSE RADIATION; GAMMA-H2AX FOCI; IONIZING-RADIATION; HUMAN-LYMPHOCYTES; CELLULAR-RESPONSES; FACILITATES REPAIR; FLOW-CYTOMETRY; IN-VITRO; DAMAGE;
D O I
10.3892/ijmm.2012.907
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In case of accidental radiation exposure or a nuclear incident, physical dosimetry is not always complete. Therefore, it is important to develop tools that allow dose estimates and determination that are based on biological markers of radiation exposure. Exposure to ionizing radiation triggers a large-scale activation of specific DNA signaling and repair mechanisms. This includes the phosphorylation of gamma H2AX in the vicinity of a double-strand break (DSB). A DNA DSB is a cytotoxic form of DNA damage, and if not correctly repaired can initiate genomic instability, chromosome aberrations, mutations or apoptosis. Measurements of DNA DSBs and their subsequent repair after in vitro irradiation has been suggested to be of potential use to monitor cellular responses. The bone marrow and the blood are known to be the most radiosensitive tissues of the human body and can therefore be of particular importance to find radiation-induced biological markers. In the present study, changes in H2AX phosphorylation and apoptosis of irradiated human peripheral blood mononuclear cells (PBMCs) were analyzed. Freshly isolated PBMCs from healthy donors were irradiated with X-rays (0.1, 0.25, 0.5, 1, 2 and 4 Gy). The phosphorylation of gamma H2AX was measured at different time points (0, 0.25, 1, 2, 4, 6 and 24 h) after irradiation. We detected a linear dose-dependency of gamma H2AX phosphorylation measured by gamma H2AX foci scoring using immunofluorescence microscopy as well as by gamma H2AX fluorescence detection using flow cytometry. Apoptosis was detected by measuring DNA fragmentation at different time points (0, 24, 48, 72, 96 h) after X-irradiation using DNA ladder gel electrophoresis. The apoptotic DNA fragmentation increased in a dose-dependent manner. In conclusion, DNA DSBs and subsequent apoptotic DNA fragmentation monitoring have potential as biomarkers for assessing human exposure in radiation biodosimetry.
引用
收藏
页码:769 / 780
页数:12
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