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阿霉素处理后处于平台期的V79细胞中潜在致死性损伤的诱导与修复证据。后处理孵育期细胞释放的阿霉素清除的重要性。

Evidence for induction and repair of potentially lethal damage in plateau-phase V79 cells after exposure to adriamycin. The importance of removal of adriamycin released from the cells during the post-treatment incubation period.

作者信息

Iliakis G

出版信息

Br J Cancer. 1987 Apr;55(4):381-4. doi: 10.1038/bjc.1987.76.

Abstract

Plateau-phase Chinese hamster V79 cells were exposed to various concentrations of adriamycin (0-21 micrograms ml-1) in conditioned medium from plateau-phase cultures (C-med). Cells were plated for colony formation, either immediately after adriamycin treatment or after a 24 h incubation either in fresh medium (F-med) or C-med. A potentiation of cell killing was observed in cells plated 24 h after treatments which was larger for cells incubated in F-med than for cells incubated in C-med. Trypsinization of the cells and replating for 24 h in the same volume of medium (total amounts of cells) but at lower surface density to reduce intercellular contact, did not modify the killing potentiation observed after delayed plating. Four to 6 changes of medium, carried out at 1 h intervals, starting immediately after treatment, led to an elimination of the killing potentiation otherwise found in cells kept after treatment in F-med and resulted in survival levels similar to those of cells plated immediately after treatment. On the other hand, survival levels higher by a factor 1.5 to 10 than those obtained for cells plated immediately after treatment were observed for cells kept in C-med when four medium changes were carried out during the first 5 h of the 6 or 24 h post-treatment period. Incubation with 150 microM beta-arabinofuranosyladenine (araA) for 6 h (C-med) after exposure to adriamycin (4 changes of medium at 1 h intervals) prevented the increase in survival observed after incubation in C-med but also caused an additional potentiation in killing resulting in survival levels lower than those of cells plated immediately after treatment. These results are interpreted as indicating the induction by adriamycin of potentially lethal damage (PLD), sensitive to araA, similar to that observed after exposure to low LET ionizing radiation. Repair and/or fixation of this form of PLD can only be shown if precautions are taken to circumvent toxicity induced by adriamycin released from the cells during the post-treatment time interval, for example, by frequent changes in medium.

摘要

处于平台期的中国仓鼠V79细胞在来自平台期培养物的条件培养基(C-培养基)中暴露于不同浓度的阿霉素(0 - 21微克/毫升)。阿霉素处理后立即或在新鲜培养基(F-培养基)或C-培养基中孵育24小时后,将细胞接种以形成集落。在处理后24小时接种的细胞中观察到细胞杀伤增强,在F-培养基中孵育的细胞比在C-培养基中孵育的细胞增强更大。将细胞胰蛋白酶消化并在相同体积的培养基(细胞总量)中以较低的表面密度重新接种24小时以减少细胞间接触,并未改变延迟接种后观察到的杀伤增强。处理后立即开始,每隔1小时进行4至6次培养基更换,导致消除了在F-培养基中处理后保留的细胞中原本发现的杀伤增强,并导致存活水平与处理后立即接种的细胞相似。另一方面,当在处理后6或24小时的前5小时内进行4次培养基更换时,对于保存在C-培养基中的细胞,观察到其存活水平比处理后立即接种的细胞高1.5至10倍。在暴露于阿霉素(每隔1小时进行4次培养基更换)后,用1​​50 microMβ-阿拉伯呋喃糖基腺嘌呤(araA)在C-培养基中孵育6小时,可防止在C-培养基中孵育后观察到的存活增加,但也会导致杀伤作用进一步增强,从而使存活水平低于处理后立即接种的细胞。这些结果被解释为表明阿霉素诱导了对araA敏感的潜在致死性损伤(PLD),类似于暴露于低LET电离辐射后观察到的情况。只有采取预防措施规避处理后时间间隔内细胞释放的阿霉素诱导的毒性,例如通过频繁更换培养基,才能显示这种形式的PLD的修复和/或固定。

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