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通过延时摄影分析佛波酯诱导的HeLa细胞G2期延迟。

Phorbol ester-induced G2 delay in HeLa cells analyzed by time lapse photography.

作者信息

Kinzel V, Bonheim G, Richards J

机构信息

Institute of Experimental Pathology, German Cancer Research Center, Heidelberg, FRG.

出版信息

Cancer Res. 1988 Apr 1;48(7):1759-62.

PMID:3349455
Abstract

The tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) has been shown previously to mimic X-irradiation in altering cell cycle parameters in Hela cells [Kinzel, V., Richards, J., and Stöhr, M., Science (Wash. DC), 210: 429-431, 1980]. These changes include a delay in G2 phase from which cells recover in the presence of TPA, which suggests an involvement of cellular mediators. In order to obtain information on the onset and the duration of the G2 delay, as well as the onset and rate of recovery, a time-lapse study has been carried out. The analysis of cells in prophase shows that at 10(-6) M and 10(-7) M concentrations, TPA and 12-O-retinoylphorbol-13-acetate (RPA) cause a G2 delay which lasts on the order of 3.5 to 4 h. Below 10(-7) M of RPA and below 10(-8) M of TPA a clear-cut inhibition of HeLa cells in G2 is no longer detectable by this method. These results for a given phorbol ester are dose dependent within a certain range but unlike the case of X-rays are not proportional to dose. Within the dose range studied the recovery rate follows the opposite order. At 10(-6) M TPA and RPA an indication of a parasynchronous burst is observed. At smaller concentrations or with less biological activity of phorbol ester, the cell multiplication rate approaches that of the control or remains even smaller. Possible reasons are discussed. The determination of the transition points seems to indicate that the cellular events inhibited in G2 occur shortly before visible prophase.

摘要

肿瘤促进剂十四烷酰佛波醇乙酯(TPA)先前已被证明在改变Hela细胞的细胞周期参数方面可模拟X射线照射[金泽尔,V.,理查兹,J.,和施托尔,M.,《科学》(华盛顿特区),210: 429 - 431,1980]。这些变化包括G2期延迟,细胞在TPA存在的情况下可从中恢复,这表明细胞介质参与其中。为了获取关于G2期延迟的起始和持续时间以及恢复的起始和速率的信息,进行了一项延时研究。对前期细胞的分析表明,在10⁻⁶ M和10⁻⁷ M浓度下,TPA和12 - O - 视黄酰佛波醇乙酯(RPA)会导致持续约3.5至4小时的G2期延迟。低于10⁻⁷ M的RPA和低于10⁻⁸ M的TPA时,用这种方法不再能检测到对HeLa细胞在G2期的明显抑制。对于给定的佛波酯,这些结果在一定范围内是剂量依赖性的,但与X射线的情况不同,它们与剂量不成正比。在所研究的剂量范围内,恢复速率遵循相反的顺序。在10⁻⁶ M的TPA和RPA时,观察到准同步爆发的迹象。在较低浓度或佛波酯生物活性较低时,细胞增殖速率接近对照或甚至更低。讨论了可能的原因。转变点的测定似乎表明在G2期被抑制的细胞事件发生在可见前期前不久。

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