TY - JOUR
T1 - Inverse dose-rate effect for mutation induction by γ-rays in human lymphoblasts
AU - Amundson, S. A.
AU - Chen, D. J.
N1 - Funding Information:
This work was performed under the auspices of the US Department of Energy under contract KP0400/005181 to the Los Alamos National Laboratory. Additional support was provided by NIH grant CA56414 to D.J.C. and a Los Alamos National Laboratory DIrector’s Postdoctoral Fellowship to S.A.A. We would like to thank H . Crissman, A. Nastasi, C. Bell-Prince, and the National Flow Resource for ¯ ow cytom etry and R. O kinaka for a critical reading of the manuscript.
PY - 1996
Y1 - 1996
N2 - In order to define further the effects of differences in recombinational proficiency on cell survival and mutation by ionizing radiation, we exposed the syngenic cell lines TK6 and WTK1 to continuous low dose-rate γ- irradiation. We previously demonstrated that acute X-ray exposure results in lower survival and lower mutation induction at both the thymidine kinase (tk) and the hypoxanthine-guanine phosphoribosyltransferase (hprt) loci in TK6 cells compared with WTK1 cells. These differences were attributed in part to reduced levels of recombination in the TK6 line relative to WTK1. Using a low dose rate 137Cs irradiator, we exposed asynchronous growing populations of these cells to γ-rays at 14.3, 6.7 and 2.7 cGy/h. Both cell lines exhibited a dose-rate effect on survival. Compared with acute doses, the low dosed- rates also protected against mutation induction at the hrpt locus in WTK1, but protection was inversely related to dose-rate. There was also a slight inverse dose-rate effect in TK6, with mutation induction at the lowest dose- rate exceeding that at acute exposures.
AB - In order to define further the effects of differences in recombinational proficiency on cell survival and mutation by ionizing radiation, we exposed the syngenic cell lines TK6 and WTK1 to continuous low dose-rate γ- irradiation. We previously demonstrated that acute X-ray exposure results in lower survival and lower mutation induction at both the thymidine kinase (tk) and the hypoxanthine-guanine phosphoribosyltransferase (hprt) loci in TK6 cells compared with WTK1 cells. These differences were attributed in part to reduced levels of recombination in the TK6 line relative to WTK1. Using a low dose rate 137Cs irradiator, we exposed asynchronous growing populations of these cells to γ-rays at 14.3, 6.7 and 2.7 cGy/h. Both cell lines exhibited a dose-rate effect on survival. Compared with acute doses, the low dosed- rates also protected against mutation induction at the hrpt locus in WTK1, but protection was inversely related to dose-rate. There was also a slight inverse dose-rate effect in TK6, with mutation induction at the lowest dose- rate exceeding that at acute exposures.
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U2 - 10.1080/095530096145562
DO - 10.1080/095530096145562
M3 - Article
C2 - 8648243
AN - SCOPUS:0029953695
SN - 0955-3002
VL - 69
SP - 555
EP - 563
JO - International Journal of Radiation Biology
JF - International Journal of Radiation Biology
IS - 5
ER -