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首页> 外文期刊>British Journal of Cancer >Enhancement of adriamycin-induced killing after delayed plating of plateau-phase V79-cells
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Enhancement of adriamycin-induced killing after delayed plating of plateau-phase V79-cells

机译:高原期V79细胞延迟铺板后阿霉素诱导的杀伤作用增强

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Unfed plateau-phase cultures of Chinese hamster V79-cells were treated for 1 h with various amounts of adriamycin in the range between 0 and 10 micrograms ml-1 and subsequently either immediately trypsinized and plated to assay for survival, or reincubated in medium collected from replicate plateau-phase cultures and returned to the incubator for various periods of time before plating. Significantly less killing was observed, for the same adriamycin dose, in cells treated in the plateau-phase and plated immediately thereafter as compared to cells treated while actively growing. When cell trypsinization and plating was delayed for up to 22 h, a significant increase in killing was observed, and the survival curve obtained approached that observed after treatment with adriamycin of growing cells. Initially almost exponential kinetics were observed for this potentiation of adriamycin-induced cell killing with a t37 of approximately 2 h. Cell survival was still decreasing after 22 h of post-treatment incubation in the plateau phase, with no clear indication for approaching a plateau. However, longer incubations, to establish a plateau, were not possible due to degeneration of the cultures. Flow cytometry measurements of the intracellular adriamycin content showed only a small difference between exponentially growing and plateau-phase cells despite the significant differences in the number of cells per culture at the time of treatment. The rate at which adriamycin-related fluorescence decayed after adriamycin treatment was slightly higher for cells trypsinized and exposed to fresh medium than for cells kept in the plateau-phase. The results indicate the importance of the physiological state and the post-treatment incubation conditions of cells for the final effect of adriamycin on survival.
机译:将中国仓鼠V79细胞的未进食的高原期培养物用0至10微克ml-1之间的各种量的阿霉素处理1 h,然后立即进行胰蛋白酶消化并接种以测定存活率,或在从复制平台期培养物,并在铺板之前的不同时间返回培养箱。与在积极生长的情况下处理的细胞相比,在相同剂量的阿霉素下,在高原期处理的细胞中观察到的杀伤力明显更低,此后立即进行了铺板。当细胞胰蛋白酶消化和铺板延迟最多22小时时,观察到杀伤力显着增加,并且获得的存活曲线接近用生长细胞阿霉素处理后观察到的存活曲线。最初观察到这种增强阿霉素诱导的细胞杀伤力的指数动力学,t37约为2小时。在平台期的后处理温育22小时后,细胞存活率仍在下降,没有明确迹象表明接近平台期。然而,由于培养物的变性,不可能进行更长的孵育以建立平台。尽管在处理时每种培养物的细胞数存在显着差异,但细胞内阿霉素含量的流式细胞仪测量显示,指数生长的细胞与平稳期细胞之间只有很小的差异。用胰蛋白酶处理并暴露于新鲜培养基的细胞,在阿霉素处理后与阿霉素相关的荧光衰减的速率略高于保持在平台期的细胞。结果表明细胞的生理状态和治疗后孵育条件对于阿霉素对生存的最终作用的重要性。

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