No abstract

DNA double strand breaks are induced by ionizing radiation (IR), leading to the phosphorylation of the core histone protein H2AX (termed cH2AX). The understanding of the cH2AX responses in irradiated human buccal cells is still very limited. We used visual scoring and laser scanning cytometry (LSC) methods to investigate cH2AX signaling following exposure of human buccal cells (from six individuals) to ionizing radiation at 0-4 Gy. The frequency of nuclei containing 15-30 cH2AX foci was significantly elevated 30 min post-IR exposure (by visual scoring). Concomitantly, there was a significant decrease in the frequency of cells without foci following exposure to IR. IR-induced cH2AX signal as determined by laser scanning cytometry (which included cH2AX integral and MaxPixel value) increased significantly in all individual's 2N nuclei 30 min post-IR and was similar for all three nuclear shapes identified. Individuals with the lowest baseline cH2AX integral (i.e., in nonirradiated cells) showed the greatest fold stimulation of cH2AX and significant dose-responses to IR doses of 1, 2, and 4 Gy. In 5 out of 6 individuals, the frequency of visually scored cH2AX in nuclei showed a strong correlation (up to r 5 0.999) with LSC scored cH2AX integrals. The cH2AX response and subsequent decline varied between individuals but remained elevated above baseline levels 24 h post IR exposure. cH2AX response in irradiated human buccal cells has potential to be used as an index of baseline DNA damage in population studies. The variable response to IR exposure between individuals should be taken into consideration when using the cH2AX assay for radiation biodosimetry. V C 2014 International Society for Advancement of Cytometry