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Apoptosis Induction by Menadione in Human Promyelocytic Leukemia HL-60 Cells

机译:甲萘醌对人早幼粒细胞白血病HL-60细胞的凋亡诱导作用

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摘要

Cell death induced by menadione (vitamin K-3,2-methyl-1,4-naphthoquinone) has been investigated in human promyelocytic leukemia HL-60 cells. Menadione was found to induce both apoptosis and necrosis in HL-60 cells. Low concentration (1~50 µM) of menadione induced apoptotic cell death, which was demonstrated by typical DNA ladder patterns on agarose gel electrophoresis and flow cytometry analysis. In contrast, a high concentration of menadione (100 µM) induced necrotic cell death, which was demonstrated by DNA smear pattern in agarose gel electrophoresis. Necrotic cell death was accompanied with a great reduction of cell viability. Menadione activated caspase-3, as evidenced by both increased protease activity and proteolytic cleavage of 116 kDa poly(ADP-ribose) polymerase (PARP) into 85 kDa cleavage product. Caspase-3 activity was maximum at 50 µM of menadione, and very low at 100 µM of menadione. Taken together, our results showed that menadi-one induced mixed types of cell death, apoptosis at low concentrations and necrosis at high concentrations in HL-60 cells.
机译:在人类早幼粒细胞白血病HL-60细胞中研究了甲萘醌(维生素K-3,2-甲基-1,4-萘醌)诱导的细胞死亡。发现甲萘醌可诱导HL-60细胞凋亡和坏死。低浓度(1〜50 µM)甲萘醌可诱导凋亡的细胞死亡,这在琼脂糖凝胶电泳和流式细胞仪分析中表现为典型的DNA梯形图。相反,高浓度的甲萘醌(100 µM)诱导坏死性细胞死亡,这在琼脂糖凝胶电泳中通过DNA涂片模式得以证实。坏死性细胞死亡伴随着细胞活力的极大降低。 Menadione激活了caspase-3,这可以通过增加蛋白酶活性和将116 kDa聚(ADP-核糖)聚合酶(PARP)的蛋白水解裂解为85 kDa裂解产物来证明。 Caspase-3活性在甲萘醌50 µM时最大,而在100μMMenadione时非常低。综上所述,我们的结果表明,甲萘醌可在HL-60细胞中诱导多种类型的细胞死亡,低浓度凋亡和高浓度坏死。

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