G2-delay after irradiation with α-particles as studied in synchronized cultures and by the bromodeoxyuridine-33258H technique
Open Access
- 1 November 1981
- Vol. 2 (3), 175-178
- https://doi.org/10.1002/cyto.990020308
Abstract
Division delay of mouse L-929 fibroblasts after α-irradiation is due to a pronounced lengthening of their G2-phase. Experiments on synchronously and asynchronously growing cultures revealed a cell cycle phasedependent sensitivity of this effect: Cells irradiated in G2 or at the Gl/S border suffered a longer G2-delay than cells irradiated at mid- or late-S. Progression through G2 was nearly normal at doses up to 0.3 Gy if cells were exposed during Gl phase.Keywords
This publication has 10 references indexed in Scilit:
- Proliferation kinetics of perturbed cell populations determined by the bromodeoxyuridine-33258 technique: Radiotoxic effects of incorporated [3H]thymidineCytometry, 1981
- The Influence of Ionization Density on the DNA Synthetic Phase and Survival of Irradiated Mammalian CellsInternational Journal of Radiation Biology, 1981
- RADIOTOXICITY OF INCORPORATED [3H]THYMIDINE AS STUDIED BY AUTORADIOGRAPHY AND FLOW CYTOMETRY CONSEQUENCES FOR THE INTERPRETATION OF FLM DATACell Proliferation, 1981
- Kinetic response of an in vitro “tumour-model” (V 79 spheroids) to 42°C hyperthermiaEuropean Journal of Cancer (1965), 1977
- G 2 Block in Chinese Hamster Cells Induced by X-Irradiation, Hyperthermia, Cycloheximide, or Actinomycin-DRadiation Research, 1976
- Optical studies of the interaction of 33258 Hoechst with DNA, chromatin, and metaphase chromosomesChromosoma, 1975