Abstract
Purpose: To test the γ-H2AX (Histone 2AX phosphorylation of serine 139) foci assay for the detection of ionising radiation-induced DNA damage in buccal exfoliated cells.Materials and methods: Buccal mucosa cells from five individuals (three females, two males, aged 26–47 years) were exposed to 0, 0.5, 1, 2 and 4 Gy of gamma-rays. DNA damage and DNA damage removal were measured using the γ-H2AX foci assay. Lymphocytes from one donor and the nuclear antigen H2B were used as a positive control to test the staining protocol.Results: In the absence of radiation exposure, no significant differences for both H2B and γ-H2AX signals were detected when comparing buccal cells and lymphocytes. The γ-H2AX foci rate per cell in non-irradiated buccal cells was 0.08 ± 0.02. The number of γ-H2AX foci increased linearly with ionising radiation dose in the interval from 0–4 Gy, and reached a foci rate per cell of 0.82 ± 0.22 at 4 Gy. Incubation experiments after in vitro gamma irradiation revealed that the number of γ-H2AX foci did not show a significant decrease 5 h post exposure under the experimental conditions used.Conclusion: Data suggest that it is possible to apply the γ-H2AX foci assay for the detection of ionising radiation-induced DNA damage in buccal exfoliated cells. The low removal of ionising radiation induced γ-H2AX foci in buccal cells is a potential advantage for a biological dosimetry application.
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