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氧化氘(重水)在分裂间期使PtK2细胞的细胞周期停滞。

Deuterium oxide (heavy water) arrests the cell cycle of PtK2 cells during interphase.

作者信息

Schroeter D, Lamprecht J, Eckhardt R, Futterman G, Paweletz N

机构信息

Institute of Cell and Tumor Biology, German Cancer Research Center, Heidelberg.

出版信息

Eur J Cell Biol. 1992 Aug;58(2):365-70.

PMID:1330569
Abstract

Deuterium oxide (D2O, heavy water) exerts an antiproliferative effect on a variety of cells in vitro and on some organisms. This effect is mainly ascribed to a tubulin-mediated antimitotic action. We evaluated the morphology, the mitotic activity, and the dynamics of the cell cycle of PtK2 cells grown in vitro in the presence of 75% D2O for up to eight weeks by microspectrophotometric DNA measurements as well as flow cytometric analysis and a determination of mitotic indices. Substitution of heavy water for water in the culture medium initially increased the mitotic index by a (pro-) metaphase block but after 2 to 3 days of incubation no mitotic figures were seen. Analysis of cells grown for 6 days in medium containing 75% D2O revealed accumulation of cells in S/G2-phase. Extended treatment stabilized the high level of cells in this specific phase, when compared to normal growing cells. Cells grown for 1 to 6 weeks in the presence of D2O remained non-proliferating, nevertheless, they were able to divide again after recovery in non-deuterated medium. The time needed for resumption of the mitotic activity was proportional to the duration of deuterium oxide exposure. Cells incubated for 8 weeks in 75% D2O did not recommence mitotic activity. Light and electron microscopic examination revealed characteristic morphological changes of size and ciliation in PtK2 cells subjected to prolonged deuteration.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

氧化氘(D2O,重水)在体外对多种细胞以及一些生物体具有抗增殖作用。这种作用主要归因于微管蛋白介导的抗有丝分裂作用。我们通过显微分光光度法DNA测量、流式细胞术分析和有丝分裂指数测定,评估了在75% D2O存在下体外培养长达8周的PtK2细胞的形态、有丝分裂活性和细胞周期动力学。在培养基中用重水替代水最初会因(前)中期阻滞而增加有丝分裂指数,但孵育2至3天后未见有丝分裂图像。对在含75% D2O的培养基中培养6天的细胞分析显示,细胞在S/G2期积累。与正常生长的细胞相比,延长处理使细胞在这个特定阶段保持高水平稳定。在D2O存在下培养1至6周的细胞仍不增殖,不过,在非重水培养基中恢复后它们能够再次分裂。恢复有丝分裂活性所需的时间与氧化氘暴露的持续时间成正比。在75% D2O中孵育8周的细胞未重新开始有丝分裂活性。光学和电子显微镜检查显示,长时间氘化处理的PtK2细胞在大小和纤毛方面有特征性形态变化。(摘要截断于250字)

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