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博来霉素处理后无毛小鼠的表皮细胞动力学。I. 不同单次剂量后的扰动

Epidermla cell kinetics in hairless mice after bleomycin. I. Perturbations after different single doses.

作者信息

Thorud E, Clausen O P

出版信息

Cancer Treat Rep. 1978 Mar;62(3):351-61.

PMID:77187
Abstract

Three different doses of bleomycin (BLM) (2,1, and 0.01 mg/animal) were injected ip into groups of hairless mice. Cell kinetic alterations in the basal layer of the epidermis were studied up to 10 days after BLM administration. The two highest doses of BLM affected the epidermal cell kinetics in a similar way but with different time courses. Only a moderate depression of the labeling index was observed during the first 24 hours. The results indicate that cells affected by BLM in the middle of the G1 phase are arrested in their subsequent S phase, and that thereafter an increase in the rate of DNA synthesis may occur in the arrested cells without increasing the number of cells in S phase. The percentage of cell accumulated in S and G2 phases as determined by flow cytofluorometry never exceeded 130% of control values with any of the doses. Phase durations were determined from percentage of labeled mitoses curves after the highest dose of BLM and were not significantly different from normal values, indicating that the accumulated cels are probably out of cycle and unable to proliferate again. Calculations based on cell counts and mitotic rate showed that the cells had a prolonged lifespan. No block and subsequent release of cells specifically caused by BLM were observed. BLM has a complex effect on the epidermis, and therefore does not seem to be a promising agent for cell synchronization as a basis for combination chemotherapy in vivo.

摘要

将三种不同剂量的博来霉素(BLM)(2、1和0.01mg/只动物)腹腔注射到无毛小鼠组中。在给予BLM后长达10天的时间里,研究了表皮基底层的细胞动力学变化。两种最高剂量的BLM对表皮细胞动力学的影响方式相似,但时间进程不同。在最初的24小时内,仅观察到标记指数有中度降低。结果表明,在G1期中期受BLM影响的细胞在随后的S期被阻滞,此后,被阻滞的细胞中DNA合成速率可能增加,而S期细胞数量并未增加。通过流式细胞荧光术测定,在任何剂量下,S期和G2期积累的细胞百分比从未超过对照值的130%。根据最高剂量BLM后的标记有丝分裂曲线百分比确定的各期持续时间与正常值无显著差异,表明积累的细胞可能脱离了细胞周期,无法再次增殖。基于细胞计数和有丝分裂率的计算表明,细胞寿命延长。未观察到由BLM特异性引起的细胞阻滞和随后的释放。BLM对表皮有复杂的作用,因此似乎不是一种有前途的用于体内联合化疗的细胞同步剂。

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