Park H J
Department of Microbiology, Inha University College of Medicine, Inchon, Korea.
Yonsei Med J. 1995 Dec;36(6):473-9. doi: 10.3349/ymj.1995.36.6.473.
The nature of the endonucleases responsible for DNA fragmentation in apoptosis has not yet been clearly defined. The intracellular acidity has been known to greatly affect apoptosis probably by affecting the activity of the endonucleases. In this study, the implication of pH in the apoptosis was investigated through the use of human HL-60 leukemia cells. The cells were incubated in media with different pH ranging from 3.5 to 7.5 for 4 hrs and the mode of cell death was investigated. The trypan blue exclusion assay showed that close to 25% and 90% of the cells were dead when incubated in pH 6.4 and pH 5.0 media, respectively. The agarose gel electrophoresis of DNA demonstrated that significant DNA fragmentation occurred in the HL-60 cells incubated in the pH 6.2-6.4 media for 4 hr indicating cell death by apoptosis. The electron microscopy study also demonstrated that many of the cells incubated in the pH 6.4 medium were in the process of apoptosis while the cells maintained in the pH 5.0 medium were dying by necrosis. The intracellular pH (pHi) of HL-60 cells was 6.6-6.9 when the extracellular pH (pHe) was 6.2-6.4. These results demonstrated that DNase I which has a maximal endonuclease activity near pH 7.0 may be responsible for the apoptosis accompanied by DNA fragmentation in HL-60 cells in the pH 6.4 medium. This observation is at variance with the previous reports that DNase II mediate the DNA fragmentation in apoptosis. The cell death at extremely low pH (pH 5.0) appeared to be due mainly to necrosis.
负责细胞凋亡中DNA片段化的核酸内切酶的性质尚未明确界定。已知细胞内酸度可能通过影响核酸内切酶的活性而极大地影响细胞凋亡。在本研究中,通过使用人HL-60白血病细胞研究了pH在细胞凋亡中的作用。将细胞在pH范围为3.5至7.5的不同培养基中孵育4小时,并研究细胞死亡方式。台盼蓝排斥试验表明,当分别在pH 6.4和pH 5.0的培养基中孵育时,分别有近25%和90%的细胞死亡。DNA的琼脂糖凝胶电泳表明,在pH 6.2 - 6.4的培养基中孵育4小时的HL-60细胞中发生了显著的DNA片段化,表明细胞通过凋亡死亡。电子显微镜研究还表明,在pH 6.4培养基中孵育的许多细胞处于凋亡过程中,而维持在pH 5.0培养基中的细胞则因坏死而死亡。当细胞外pH(pHe)为6.2 - 6.4时,HL-60细胞的细胞内pH(pHi)为6.6 - 6.9。这些结果表明,在pH 7.0附近具有最大内切酶活性的DNase I可能是pH 6.4培养基中HL-60细胞伴随DNA片段化的凋亡的原因。这一观察结果与之前关于DNase II介导细胞凋亡中DNA片段化的报道不一致。在极低pH(pH 5.0)下的细胞死亡似乎主要是由于坏死。