Liu X, Kim C N, Yang J, Jemmerson R, Wang X
Department of Biochemistry, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Cell. 1996 Jul 12;86(1):147-57. doi: 10.1016/s0092-8674(00)80085-9.
A cell-free system based on cytosols of normally growing cells is established that reproduces aspects of the apoptotic program in vitro. The apoptotic program is initiated by addition of dATP. Fractionation of cytosol yielded a 15 kDa protein that is required for in vitro apoptosis. The absorption spectrum and protein sequence revealed that this protein is cytochrome c. Elimination of cytochrome c from cytosol by immunodepletion, or inclusion of sucrose to stabilize mitochondria during cytosol preparation, diminished the apoptotic activity. Adding back cytochrome c to the cytochrome c-depleted extracts restored their apoptotic activity. Cells undergoing apoptosis in vivo showed increased release of cytochrome c to their cytosol, suggesting that mitochondria may function in apoptosis by releasing cytochrome c.
建立了一种基于正常生长细胞胞质溶胶的无细胞系统,该系统可在体外重现凋亡程序的某些方面。凋亡程序通过添加dATP启动。对胞质溶胶进行分级分离得到一种15 kDa的蛋白质,它是体外凋亡所必需的。吸收光谱和蛋白质序列表明该蛋白质是细胞色素c。通过免疫去除从胞质溶胶中消除细胞色素c,或在制备胞质溶胶期间加入蔗糖以稳定线粒体,均可降低凋亡活性。将细胞色素c添加回细胞色素c缺失的提取物中可恢复其凋亡活性。体内发生凋亡的细胞显示细胞色素c向其胞质溶胶中的释放增加,这表明线粒体可能通过释放细胞色素c在凋亡中发挥作用。