葡萄孢霉素
细胞色素c
细胞凋亡
线粒体凋亡诱导通道
线粒体
细胞生物学
生物
膜电位
细胞色素
细胞色素b
线粒体内膜
凋亡体
程序性细胞死亡
线粒体DNA
分子生物学
半胱氨酸蛋白酶
生物化学
信号转导
蛋白激酶C
基因
酶
作者
Pablo M. Peixoto,Shin-Young Ryu,Agnès Bombrun,Bruno Antonsson,Kathleen W. Kinnally
摘要
MAC (mitochondrial apoptosis-induced channel) forms in the mitochondrial outer membrane and unleashes cytochrome c to orchestrate the execution of the cell. MAC opening is the commitment step of intrinsic apoptosis. Hence closure of MAC may prevent apoptosis. Compounds that blocked the release of fluorescein from liposomes by recombinant Bax were tested for their ability to directly close MAC and suppress apoptosis in FL5.12 cells. Low doses of these compounds (IC50 values ranged from 19 to 966 nM) irreversibly closed MAC. These compounds also blocked cytochrome c release and halted the onset of apoptotic markers normally induced by IL-3 (interleukin-3) deprivation or staurosporine. Our results reveal the tight link among MAC activity, cytochrome c release and apoptotic death, and indicate this mitochondrial channel is a promising therapeutic target.
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