Barranco S C, Haenelt B R, Bolton W E
Cell Tissue Kinet. 1977 Jul;10(4):335-40. doi: 10.1111/j.1365-2184.1977.tb00301.x.
Following a 10 min pulse labeling with 3H-TdR, flasks of asynchronous monolayer cultures of Chinese hamster ovary cells were subjected to mitotic selection at 2 hr intervals. The mitotic index of the selected populations was always greater than 90%. Counts per min per cell obtained by liquid scintillation counting were plotted versus time after the pulse label. Comparisons were made between cycle times obtained by the mitotic-scintillation counting method and by the standard per cent labeled mitosis technique. The resulting curves were used for calculations of the cell cycle times and the lengths of G1, S, G2 and M phases of the cell cycle. There was less than 2% difference in the cell cycle times obtained using the scintillation method as compared to times calculated from autoradiographic data obtained from individual petri dishes. The mitotic-scintillation counting technique is simple, accurate and rapid and allows the calculation of the cell kinetics parameters within 1 hr of the end of the experiment.
用³H-TdR进行10分钟脉冲标记后,每隔2小时对中国仓鼠卵巢细胞的异步单层培养瓶进行有丝分裂选择。所选群体的有丝分裂指数始终大于90%。通过液体闪烁计数获得的每细胞每分钟计数与脉冲标记后的时间作图。对通过有丝分裂闪烁计数法和标准标记有丝分裂百分比技术获得的细胞周期时间进行了比较。所得曲线用于计算细胞周期时间以及细胞周期中G1、S、G2和M期的时长。与根据单个培养皿的放射自显影数据计算出的时间相比,使用闪烁法获得的细胞周期时间差异小于2%。有丝分裂闪烁计数技术简单、准确、快速,并且能够在实验结束后1小时内计算细胞动力学参数。