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Cyclic X-Ray Responses in Mammalian Cells in Vitro

Warren K. Sinclair
Radiation Research
Vol. 33, No. 3 (Mar., 1968), pp. 620-643
DOI: 10.2307/3572419
Stable URL: http://www.jstor.org/stable/3572419
Page Count: 24
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Cyclic X-Ray Responses in Mammalian Cells in Vitro
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Abstract

Various radiation responses in mammalian cells depend on the position of the cell within its generation cycle (that is, its age) at the time of irradiation. Studies have most often been made by irradiating synchronized populations of cells in vitro. Results in different cell lines are not easy to compare, but an attempt has been made here to point out similarities and differences with regard to cell killing and division delay. In general, survival data obtained so far show that, in cells with a short G1, cells are most sensitive in mitosis and in G2, less sensitive in G1, and least sensitive during the latter part of the S period. In cells with a long G1, in addition to the above, there is usually a resistant phase early in G1 followed by a sensitive stage near its end. (The latter may be as sensitive as mitosis.) Exceptions to the above, especially in some L cell sublines, have been noted, and a possible explanation is given. In Chinese hamster cells, maximum survival after irradiation occurs during S, but it does not coincide with the time of the maximum rate of DNA synthesis or with the time of the maximum number of cells in DNA synthesis, and changes in survival also occur in cells inhibited from synthesizing DNA. Rather, survival depends on the position the cell has reached in the cycle at that time, which involves not only DNA synthesis but other processes as well. Survival is not completely correlated with DNA synthesis, since halting DNA synthesis just before or just after irradiation only slightly affects survival at its maximum. Division delay exhibits a pattern of response which is similar in most cell lines. Delay is considerable for cells irradiated in mitosis, is small for cells in G1, increases to a maximum for cells during S, and declines for cells in G2. L cells or human kidney cells may have a longer delay for cells irradiated in G2 than for those irradiated in S. The results can be explained in terms of a two-component model of division delay. One component results from the prolongation of the S period due to the reduced rate of DNA synthesis, and the other, a block in G2, is independent of DNA synthesis. The proportion of the two components may vary in different cell lines.

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