Zhu H, Fearnhead H O, Cohen G M
MRC Toxicology Unit, University of Leicester, UK.
FEBS Lett. 1995 Oct 30;374(2):303-8. doi: 10.1016/0014-5793(95)01116-v.
Apoptosis was induced in THP.1 cells, a human monocytic tumour cell line, by diverse stimuli including cycloheximide, thapsigargin, etoposide and staurosporine. Induction of apoptosis by all these stimuli, except etoposide, was enhanced in the presence of the trypsin-like protease inhibitor, N alpha-tosyl-L-lysinyl chloromethyl ketone (TLCK). Induction of apoptosis, assessed by morphological, flow cytometric and biochemical criteria, including proteolysis of poly(ADP-ribose) polymerase and cleavage of DNA to large kilobasepair fragments, was completely abrogated when cells were pretreated with an ICE-like protease inhibitor, Z-Val-Ala-Asp.fluoromethylketone. This suggested that an ICE homologue was a common mediator of apoptosis in THP.1 cells.
通过包括放线菌酮、毒胡萝卜素、依托泊苷和星形孢菌素在内的多种刺激,在人单核细胞肿瘤细胞系THP.1细胞中诱导凋亡。除依托泊苷外,在胰蛋白酶样蛋白酶抑制剂Nα-甲苯磺酰-L-赖氨酰氯甲基酮(TLCK)存在的情况下,所有这些刺激诱导的凋亡均增强。当细胞用ICE样蛋白酶抑制剂Z-Val-Ala-Asp.氟甲基酮预处理时,通过形态学、流式细胞术和生化标准(包括聚(ADP-核糖)聚合酶的蛋白水解和DNA切割成大的千碱基对片段)评估的凋亡诱导被完全消除。这表明ICE同源物是THP.1细胞凋亡的常见介质。