Mortensen B T, Hartmann N R, Christensen I J, Larsen J K, Kristensen T, Wieslander S B, Nissen N I
Cell Tissue Kinet. 1986 May;19(3):351-64. doi: 10.1111/j.1365-2184.1986.tb00686.x.
Cultures of the promyelocytic cell line HL 60 were synchronized with thymidine. A concentration of 0.05 mM thymidine and an exposure time of 24 hr was found optimal for blocking about 90% of the cells in S phase. Following release from the thymidine block the cell cultures were followed intermittently over 40 hr for fluctuation in cell numbers, labelling with radioactive thymidine and nuclear DNA distributions. Mathematical evaluation of the results revealed a cycling time of 18.6 hr and a duration of specific cell phases of 8.6 hr, 7.1 hr and 2.9 hr for G1, S and G2 + M, respectively. The doubling time was 26 hr and the growth fraction was estimated as 1.
早幼粒细胞系HL 60的培养物用胸苷进行同步化处理。发现浓度为0.05 mM的胸苷和24小时的暴露时间最适合将约90%的细胞阻滞在S期。从胸苷阻滞中释放后,对细胞培养物进行了40小时的间歇性跟踪,观察细胞数量的波动、放射性胸苷标记和核DNA分布。对结果的数学评估显示,细胞周期时间为18.6小时,G1、S和G2 + M期的特定细胞阶段持续时间分别为8.6小时、7.1小时和2.9小时。倍增时间为26小时,生长分数估计为1。