Chemical protection and cell‐cycle effects on radiation‐induced mutagenesis

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Abstract
Chinese hamster ovary cells in the exponential phase of growth were harvested and separated by the method of centrifugal elutriation into subpopulations enriched with up to 95% G1 phase, 70% S phase and 65% G2+ M phase cells. Cell cycle distributions were routinely monitored by flow cytometry. Following elutriation, aliquots of cells from each of the enriched cell fractions were incubated in the presence or absence of 4 MM of 2–[(aminopropyl)amino] ethanethiol (WR‐1065) for 30 min at 37°C. The cells were then irradiated with 60Co γ‐rays or fission‐spectrum neutrons from the JANUS research reactor. Both cell killing and mutagenesis were determined. Regardless of the radiation quality used, cells enriched in G1 phase were the most sensitive to radiation‐induced mutagenesis at the hypoxanthine‐guanine phos‐phoribosyl transferase locus. The relative magnitude of protection exerted by WR‐1065 differed for each of the elutriator separated cell populations. The greatest magnitude of protection, however, was observed for G1‐enriched populations, regardless of the radiation quality used or the biological end‐point tested.