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热疗后酸性环境下的细胞凋亡及细胞周期进程紊乱

Apoptosis and perturbation of cell cycle progression in an acidic environment after hyperthermia.

作者信息

Takasu T, Lyons J C, Park H J, Song C W

机构信息

Department of Therapeutic Radiology-Radiation Oncology, University of Minnesota Medical School, Minneapolis 55455, USA.

出版信息

Cancer Res. 1998 Jun 15;58(12):2504-8.

PMID:9635568
Abstract

The effects of an acidic environment on the induction of apoptosis by 42 degrees C hyperthermia were investigated. An acidic environment (pH 6.6) enhanced the hyperthermia-induced apoptosis in HL-60 human promyelocytic leukemia cells as judged by the DNA fragmentation, flow cytometric analysis of DNA content, and cleavage of poly(ADP-ribose) polymerase. Hyperthermia exerted no effect on the expression of Bcl-2 and Bax, regardless of the environmental acidity during heating. The time of increase in apoptosis after heating coincided with the time of decrease in the G1-phase cell population. It seemed that the increase in heat-induced apoptosis in HL-60 cells in an acidic environment was due to a direct increase in the proteolytic cleavage of poly(ADP-ribose) polymerase by acidic caspases without the involvement of Bcl-2 and Bax, and that heat-induced apoptosis occurred during G1 phase in HL-60 cells.

摘要

研究了酸性环境对42℃高温诱导细胞凋亡的影响。通过DNA片段化、DNA含量的流式细胞术分析以及聚(ADP-核糖)聚合酶的裂解判断,酸性环境(pH 6.6)增强了HL-60人早幼粒细胞白血病细胞中高温诱导的细胞凋亡。无论加热期间的环境酸度如何,高温对Bcl-2和Bax的表达均无影响。加热后细胞凋亡增加的时间与G1期细胞群体减少的时间一致。似乎酸性环境中HL-60细胞热诱导凋亡的增加是由于酸性半胱天冬酶直接增加了聚(ADP-核糖)聚合酶的蛋白水解裂解,而不涉及Bcl-2和Bax,并且热诱导凋亡发生在HL-60细胞的G1期。

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