Nishihara T, Akifusa S, Koseki T, Kato S, Muro M, Hanada N
Department of Oral Science, National Institute of Health, Tokyo, Japan.
Biochem Biophys Res Commun. 1995 Jul 6;212(1):255-62. doi: 10.1006/bbrc.1995.1964.
Concanamycin A and bafilomycin A1 are known as strong inhibitors of the vacuolar type H(+)-ATPases in vitro. These inhibitors exhibited cytotoxic effects on twelve cell lines in cell viability assay. On the other hand, the F1F0-type H(+)-ATPase inhibitor oligomycin and the E1E2-type H(+)-ATPase inhibitor vanadate showed no cytotoxic effect. We show here that concanamycin A and bafilomycin A1 induce a significant increase in the proportion of fragmented DNA in agarose gel electrophoresis. Flow cytometric cell cycle analysis of WEHI 231 cells stimulated with concanamycin A revealed the increased percentage of apoptotic cells with hypodiploid DNA. These findings indicate that cell death induced by specific inhibitors of vacuolar type H(+)-ATPases occurs through apoptosis.
concanamycin A和bafilomycin A1在体外被认为是液泡型H(+) -ATP酶的强抑制剂。在细胞活力测定中,这些抑制剂对12种细胞系表现出细胞毒性作用。另一方面,F1F0型H(+) -ATP酶抑制剂寡霉素和E1E2型H(+) -ATP酶抑制剂钒酸盐未显示出细胞毒性作用。我们在此表明,concanamycin A和bafilomycin A1在琼脂糖凝胶电泳中可导致DNA片段化比例显著增加。用concanamycin A刺激的WEHI 231细胞的流式细胞术细胞周期分析显示,具有亚二倍体DNA的凋亡细胞百分比增加。这些发现表明,液泡型H(+) -ATP酶的特异性抑制剂诱导的细胞死亡是通过凋亡发生的。