凋亡体
细胞凋亡
细胞色素c
内源性凋亡
半胱氨酸蛋白酶
程序性细胞死亡
坏死
细胞内
细胞生物学
Jurkat细胞
线粒体
化学
生物
分子生物学
生物化学
免疫学
T细胞
遗传学
免疫系统
作者
Yoshiro Saito,Keiko Nishio,Yoko Ogawa,Junko Kimata,Tomoya Kinumi,Yasukazu Yoshida,Noriko Noguchi,Etsuo Niki
标识
DOI:10.1080/10715760600632552
摘要
The turning point between apoptosis and necrosis induced by hydrogen peroxide (H2O2) have been investigated using human T-lymphoma Jurkat cells. Cells treated with 50 microM H2O2 exhibited caspase-9 and caspase-3 activation, finally leading to apoptotic cell death. Treatment with 500 microM H2O2 did not exhibit caspase activation and changed the mode of death to necrosis. On the other hand, the release of cytochrome c from the mitochondria was observed under both conditions. Treatment with 500 microM H2O2, but not with 50 microM H2O2, caused a marked decrease in the intracellular ATP level; this is essential for apoptosome formation. H2O2-reducing enzymes such as cellular glutathione peroxidase (cGPx) and catalase, which are important for the activation of caspases, were active under the 500 microM H2O2 condition. Prevention of intracellular ATP loss, which did not influence cytochrome c release, significantly activated caspases, changing the mode of cell death from necrosis to apoptosis. These results suggest that ATP-dependent apoptosome formation determines whether H2O2-induced cell death is due to apoptosis or necrosis.
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