Induction of mitochondrial dysfunction by poly(ADP-ribose) polymer: Implication for neuronal cell death

Poly(ADP-ribose) polymerase-1 (PARP-1) mediates neuronal cell death in a variety of pathological conditions involving severe DNA damage. Poly(ADP-ribose) (PAR) polymer is a product synthesized by PARP-1. Previous studies suggest that PAR polymer heralds mitochondrial apoptosis-inducing factor (AIF)...

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Veröffentlicht in:Molecules and cells 2013, 36(3), , pp.258-266
Hauptverfasser: Baek, S.H., Ajou University, Suwon, Republic of Korea, Bae, O.N., Hanyang University, Ansan, Republic of Korea, Kim, E.K., Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, Republic of Korea, Yu, S.W., Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, Republic of Korea
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Sprache:eng
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Zusammenfassung:Poly(ADP-ribose) polymerase-1 (PARP-1) mediates neuronal cell death in a variety of pathological conditions involving severe DNA damage. Poly(ADP-ribose) (PAR) polymer is a product synthesized by PARP-1. Previous studies suggest that PAR polymer heralds mitochondrial apoptosis-inducing factor (AIF) release and thereby, signals neuronal cell death. However, the details of the effects of PAR polymer on mitochondria remain to be elucidated. Here we report the effects of PAR polymer on mitochondria in cells in situ and isolated brain mitochondria in vitro. We found that PAR polymer causes depolarization of mitochondrial membrane potential and opening of the mitochondrial permeability transition pore early after injury. Furthermore, PAR polymer specifically induces AIF release, but not cytochrome c from isolated brain mitochondria. These data suggest PAR polymer as an endogenous mitochondrial toxin and will further our understanding of the PARP-1-dependent neuronal cell death paradigm.
ISSN:1016-8478
0219-1032
DOI:10.1007/s10059-013-0172-0