Abstract
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 me 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.
| Original language | English |
|---|---|
| Pages (from-to) | 6165-6178 |
| Number of pages | 14 |
| Journal | Journal of Neuroscience |
| Volume | 17 |
| Issue number | 16 |
| DOIs | |
| State | Published - Aug 15 1997 |
ASJC Scopus Subject Areas
- General Neuroscience
Keywords
- Apoptosis
- Caspase
- Cell-free
- Mastoparan
- Mitochondria
- Neuronal
- Protease
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