Abstract

The kinetics of the formation of cells carrying micronuclei (MN) after one doubling time (td) incorporation of 125I-iododeoxyuridine (125IdU) to Chinese hamster ovary (CHO) and rat anterior pituitary tumor (GC) cells was studied. Uptake of 125IdU by cells of both cell lines was linearly dependent on the concentration of extracellular 125I activity. The postlabeling time-dependent decrease in cellular activity of 125IdU was exponential in CHO cells and approximately linear in GC cells. The maximum yield of MN was seen during the second and third td after 125IdU incorporation. The frequency of cells with micronuclei increased monotonically with dose in the interval (1, 40) 125I decays cell-1td-1. The dose-response relationship could be fitted by straight lines with slopes of 1.0 (CHO) and 1.2 (GC) on the subinterval (1, 10) and of 0.6 or 0.5, respectively, for the subinterval (10, 40). Below one 125I decay cell-1td-1, the mean frequency of micronucleated binuclear cells was significantly lower than (CHO) or equal to (GC) the control. On average, one 125I decay/cell induced 0.95 +/- 0.5% (CHO) or 1.0 +/- 0.5% (GC) of micronucleated binuclear cells.

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