Suppr超能文献

玫瑰树碱对培养的哺乳动物细胞存活及细胞周期进程的影响。

Effects of ellipticine on cell survival and cell cycle progression in cultured mammalian cells.

作者信息

Traganos F, Staiano-Coico L, Darzynkiewicz Z, Melamed M R

出版信息

Cancer Res. 1980 Jul;40(7):2390-9.

PMID:6155993
Abstract

The effects of ellipticine [5,11-dimethyl-6H-pyrido(4,3-b)carbazole; NSC 71795] on cell viability, growth, and colony formation were investigated in suspension (Friend leukemia and L1210) and adherent [Chinese hamster ovary (CHO)]tumor cell systems as well as in mitogen-stimulated human peripheral blood lymphocyte cultures. Cell cycle progression and the terminal point of action of the drug were monitored by flow cytometry. Ellipticine was cytostatic for all cell lines tested, blocking cells in G2 phase following 24 hr constant exposure at concentrations in the range of 1.0 microgram/ml. A 10 times higher drug concentration was required to block cells in G2 if the cells were exposed for only 30 min to the drug followed by 23.5 hr culture in drug-free medium. Formation of CHO cell colonies was inhibited by 50% following exposure to ellipticine for 2 hr at 6.0 microgram/ml or for 24 hr at 0.3 microgram/ml. Fifty % cell kill in asynchronously growing Friend leukemia and L1210 cells was obtained following exposure to ellipticine for 24 hr at 2.0 microgram/ml and 1.15 microgram/ml, respectively, whereas human peripheral blood lymphocytes required 66 hr exposure to 1.0 microgram/ml to kill 50% of the cells. Phytohemagglutinin-stimulated lymphocytes were remarkably resistant to the cytotoxic effect of ellipticine but did display a dose-dependent inhibition of stimulation and accumulation in G2 whether the drug was added prior to our during active cell proliferation. Ellipticine, at cytostatic concentrations, had a marked effect on cellular RNA content. Friend leukemia cells, blocked in G2 by the drug, doubled their RNA content compared to control cells. L1210 and CHO cells, but not lymphocytes, also increased in RNA content following ellipticine treatment. Drug concentrations which blocked cells in G2 also led in the case of Friend leukemia and L1210 but not CHO cells to an increase in the proportion of cells with greater than 4C amounts of DNA.

摘要

研究了玫瑰树碱[5,11 - 二甲基 - 6H - 吡啶并(4,3 - b)咔唑;NSC 71795]对悬浮培养的(弗瑞德白血病细胞和L1210细胞)以及贴壁培养的[中国仓鼠卵巢(CHO)]肿瘤细胞系的细胞活力、生长和集落形成的影响,同时也研究了其对有丝分裂原刺激的人外周血淋巴细胞培养物的影响。通过流式细胞术监测细胞周期进程和该药物的作用终点。玫瑰树碱对所有测试的细胞系均有细胞生长抑制作用,在1.0微克/毫升的浓度下持续暴露24小时后,可使细胞阻滞于G2期。如果细胞仅暴露于该药物30分钟,随后在无药培养基中培养23.5小时,则需要高出10倍的药物浓度才能使细胞阻滞于G2期。在6.0微克/毫升的浓度下暴露2小时或在0.3微克/毫升的浓度下暴露24小时后,玫瑰树碱可使CHO细胞集落形成受到50%的抑制。在异步生长的弗瑞德白血病细胞和L1210细胞中,分别在2.0微克/毫升和1.15微克/毫升的浓度下暴露24小时后,可使50%的细胞死亡,而人外周血淋巴细胞需要在1.0微克/毫升的浓度下暴露66小时才能使50%的细胞死亡。植物血凝素刺激的淋巴细胞对玫瑰树碱的细胞毒性作用具有显著抗性,但无论在活跃细胞增殖之前还是期间添加该药物,均表现出剂量依赖性的刺激抑制和G2期细胞积累。在细胞生长抑制浓度下,玫瑰树碱对细胞RNA含量有显著影响。被该药物阻滞于G2期的弗瑞德白血病细胞,其RNA含量相对于对照细胞增加了一倍。经玫瑰树碱处理后,L1210细胞和CHO细胞(但淋巴细胞除外)的RNA含量也有所增加。在弗瑞德白血病细胞和L1210细胞中,使细胞阻滞于G2期的药物浓度还导致DNA含量大于4C的细胞比例增加,但CHO细胞未出现这种情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验