Charp P A, Kinders R J, Johnson T C
J Cell Biol. 1983 Aug;97(2):311-6. doi: 10.1083/jcb.97.2.311.
The ability of glycopeptides, isolated from bovine cerebral cortex, to alter cell division was studied by cell-cycle analyses. The results showed that glycopeptides arrested baby hamster kidney (BHK)-21 cells and Chinese hamster ovary (CHO) cells in the G2 phase of the cell cycle. Upon removal of the growth inhibition from arrested BHK-21 cells, the mitotic index in colchicine-treated cultures increased from 5 to 40% within 6 h and the increase in mitotic activity was accompanied by a complete doubling of all arrested cells within this 6-h time period. Determination of DNA content in growth-arrested BHK-21 cells showed that growth-arrested cells contained about twice the DNA of control cell cultures. Although CHO cells treated in a like manner with growth inhibitor could not be arrested for the same length of time as BHK-21 cells (18 h vs. 72 h before initiation of escape) and to the same degree (60% of the cell population vs. 99% of BHK-21 cells), the escape kinetics of CHO cells did indicate a G2 arrest. Approximately 3.5 h after escape began, CHO cell numbers in treated cultures attained the cell numbers found in control cultures. This rapid growth phase occurring in less than 4 h indicated that the growth inhibitor induced a G2 arrest-point in CHO cells that was not lethal since the entire arrested cell population divided.
通过细胞周期分析研究了从牛大脑皮层分离出的糖肽改变细胞分裂的能力。结果表明,糖肽使仓鼠肾(BHK)-21细胞和中国仓鼠卵巢(CHO)细胞停滞在细胞周期的G2期。在去除停滞的BHK-21细胞的生长抑制后,秋水仙碱处理的培养物中的有丝分裂指数在6小时内从5%增加到40%,并且有丝分裂活性的增加伴随着在这6小时内所有停滞细胞完全翻倍。对生长停滞的BHK-21细胞的DNA含量测定表明,生长停滞的细胞所含DNA约为对照细胞培养物的两倍。尽管以同样方式用生长抑制剂处理的CHO细胞不能像BHK-21细胞那样停滞相同的时间(逃脱前分别为18小时和72小时),也不能达到相同的程度(细胞群体的60%对BHK-21细胞的99%),但CHO细胞的逃脱动力学确实表明存在G2期停滞。逃脱开始后约3.5小时,处理培养物中的CHO细胞数量达到对照培养物中的细胞数量。在不到4小时内出现的这种快速生长阶段表明,生长抑制剂在CHO细胞中诱导了一个非致死性的G2停滞点,因为整个停滞的细胞群体都进行了分裂。