Ellerby H M, Martin S J, Ellerby L M, Naiem S S, Rabizadeh S, Salvesen G S, Casiano C A, Cashman N R, Green D R, Bredesen D E
The Burnham Institute, La Jolla Cancer Research Center, La Jolla, California 92037, USA.
J Neurosci. 1997 Aug 15;17(16):6165-78.
Apoptosis is a fundamental process required for normal development of the nervous system and is triggered during neurodegenerative disease. To dissect the molecular events leading to neuronal cell death, we have developed a cell-free model of neuronal apoptosis. The model faithfully reproduces key elements of apoptosis, including chromatin condensation, DNA fragmentation, caspase activation/processing, and selective substrate cleavage. We report that cell-free apoptosis is activated in premitochondrial, mitochondrial, and postmitochondrial phases by tamoxifen, mastoparan, and cytochrome c, respectively, allowing a functional ordering of these proapoptotic modulators. Furthermore, this is the first report of mitochondrial-mediated activation of cell-free apoptosis in a cell extract. Although Bcl-2 blocks activation at the premitochondrial and mitochondrial levels, it does not affect the postmitochondrial level. The cell-free system described here provides a valuable tool to elucidate the molecular events leading to neuronal cell death.
细胞凋亡是神经系统正常发育所必需的基本过程,并且在神经退行性疾病期间被触发。为了剖析导致神经元细胞死亡的分子事件,我们开发了一种神经元细胞凋亡的无细胞模型。该模型忠实地再现了细胞凋亡的关键要素,包括染色质浓缩、DNA片段化、半胱天冬酶激活/加工以及选择性底物切割。我们报告,无细胞凋亡分别在前期线粒体、线粒体和后期线粒体阶段被他莫昔芬、马斯托帕兰和细胞色素c激活,从而对这些促凋亡调节剂进行功能排序。此外,这是关于细胞提取物中线粒体介导的无细胞凋亡激活的首次报道。虽然Bcl-2在前期线粒体和线粒体水平阻断激活,但它不影响后期线粒体水平。这里描述的无细胞系统为阐明导致神经元细胞死亡的分子事件提供了一个有价值的工具。