Leroy F, Van Hoeck J, Bogaert C
Cell Tissue Kinet. 1977 Sep;10(5):437-45. doi: 10.1111/j.1365-2184.1977.tb00862.x.
Cell kinetics in the uterine epithelium of ovariectomized rats were studied after uterine distension and/or an oestradiol injection, by cumulative 3H-TdR labelling and percentage of labelled mitoses (PLM). With both methods it was found that distension shortens the total cell cycle at the expense of G1 more than does oestradiol. Both treatments act in a cumulative manner since the greatest reduction in T c is observed after distension plus oestradiol. PLM curves showed that distension and/or oestradiol induce a 30% reduction S phase duration. The evolution of percentages of labelled cells and colchicine-blocked mitoses after these treatments confirms their additive effects and indicates that the mitogenic action of oestradiol is delayed compared to that of distension. It is suggested that these factors stimulate epithelial cell division in the uterus through partly different metabolic channels.
通过累积³H-胸腺嘧啶核苷标记法和标记有丝分裂百分数(PLM),研究了子宫扩张和/或注射雌二醇后去卵巢大鼠子宫上皮细胞的动力学。两种方法均发现,与雌二醇相比,子宫扩张以牺牲G1期为代价更能缩短总细胞周期。两种处理具有累积作用,因为在子宫扩张加雌二醇处理后观察到Tc的最大缩短。PLM曲线表明,子宫扩张和/或雌二醇可使S期持续时间缩短30%。这些处理后标记细胞百分数和秋水仙碱阻断有丝分裂的变化证实了它们的相加作用,并表明与子宫扩张相比,雌二醇的促有丝分裂作用延迟。提示这些因素通过部分不同的代谢途径刺激子宫上皮细胞分裂。