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Mitochondria and programmed cell death: back to the future

Abstract : Programmed cell death, or apoptosis, has in the past few years undoubtedly become one of the most intensively investigated biological processes. However, fundamental queslions concerning the molecular and biochemical mechanisms remain to be elucidated. The central question concerns the biochemical steps shared by the numerous death induction pathways elicited by different stimuli. Heterogeneous death signals precede a common effector phase during which cells pass a threshold of'no return' and are engaged in a degradation phase where they acquire the typical onset of late apoptosis. Alterations in mitochondrial permeability transition linked to membrane potential disruption precede nuclear and plasma membrane changes. In vitro induction of permeability transition in isolated mitochondria provokes the release of a protein factor capable of inducing nuclear chromatin condensation and fragmentation. Yhis permeability transition is regulated by multiple endogenous effectors, including members of the bcl-2 gene family. Inhibition of these effects prevents apoptosis.
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Contributor : Bernard Mignotte Connect in order to contact the contributor
Submitted on : Friday, December 18, 2020 - 4:41:11 PM
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  • HAL Id : hal-03038592, version 1



Patrice X Petit, Santos-Antonio Susin, Naoufal Zamzami, Bernard Mignotte, Guido Kroemer. Mitochondria and programmed cell death: back to the future. FEBS Letters, Wiley, 1996, 396, pp.7-13. ⟨hal-03038592⟩



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