| Autor: |
Precht, T.A., Phelps, R.A., Linseman, D.A., Butts, B.D., Le, S.S., Laessig, T.A., Bouchard, R.J., Heidenreich, K.A. |
| Předmět: |
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| Zdroj: |
Cell Death & Differentiation; Mar2005, Vol. 12 Issue 3, p255-265, 11p |
| Abstrakt: |
Cerebellar granule neurons (CGNs) require depolarization for their survival in culture. When deprived of this stimulus, CGNs die via an intrinsic apoptotic cascade involving Bim induction, Bax translocation, cytochrome c release, and caspase-9 and -3 activation. Opening of the mitochondrial permeability transition pore (mPTP) is an early event during intrinsic apoptosis; however, the precise role of mPTP opening in neuronal apoptosis is presently unclear. Here, we show that mPTP opening acts as an initiating event to stimulate Bax translocation to mitochondria. A C-terminal (a9 helix) GFP-Bax point mutant (T182A) that constitutively localizes to mitochondria circumvents the requirement for mPTP opening and is entirely sufficient to induce CGN apoptosis. Collectively, these data indicate that the major role of mPTP opening in CGN apoptosis is to trigger Bax translocation to mitochondria, ultimately leading to cytochrome c release and caspase activation.Cell Death and Differentiation (2005) 12, 255-265. doi:10.1038/sj.cdd.4401552 Published online 7 January 2005 [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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