Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release

Poly(ADP-ribose) polymerase-1-dependent cell death (known as parthanatos) plays a pivotal role in many clinically important events including ischaemia/reperfusion injury and glutamate excitotoxicity. A recent study by us has shown that uncleaved AIF (apoptosis-inducing factor), but not calpain-hydro...

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Main Authors: Seong-Woon Yu, Yingfei Wang, Didrik S Frydenlund, Ole Petter Ottersen, Valina L Dawson, Ted M Dawson
Format: Article
Language:English
Published: SAGE Publishing 2009-10-01
Series:ASN Neuro
Online Access:https://doi.org/10.1042/AN20090046
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spelling doaj-0412ba98a25a4c9fa458939be561e6622020-11-25T03:15:47ZengSAGE PublishingASN Neuro1759-09141759-90912009-10-01110.1042/AN2009004610.1042_AN20090046Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for ReleaseSeong-Woon Yu0Yingfei Wang1Didrik S Frydenlund2Ole Petter Ottersen3Valina L Dawson4Ted M Dawson5 Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, U.S.A. Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, U.S.A. Centre for Molecular Biology and Neuroscience, Institute of Basic Medical Sciences, University of Oslo, POB 1105, Blindern, N-0317, Oslo, Norway Centre for Molecular Biology and Neuroscience, Institute of Basic Medical Sciences, University of Oslo, POB 1105, Blindern, N-0317, Oslo, Norway Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, U.S.A. Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, U.S.A.Poly(ADP-ribose) polymerase-1-dependent cell death (known as parthanatos) plays a pivotal role in many clinically important events including ischaemia/reperfusion injury and glutamate excitotoxicity. A recent study by us has shown that uncleaved AIF (apoptosis-inducing factor), but not calpain-hydrolysed truncated-AIF, was rapidly released from the mitochondria during parthanatos, implicating a second pool of AIF that might be present in brain mitochondria contributing to the rapid release. In the present study, a novel AIF pool is revealed in brain mitochondria by multiple biochemical analyses. Approx. 30% of AIF loosely associates with the outer mitochondrial membrane on the cytosolic side, in addition to its main localization in the mitochondrial intermembrane space attached to the inner membrane. Immunogold electron microscopic analysis of mouse brain further supports AIF association with the outer, as well as the inner, mitochondrial membrane in vivo . In line with these observations, approx. 20% of uncleaved AIF rapidly translocates to the nucleus and functionally causes neuronal death upon NMDA ( N -methyl- d -aspartate) treatment. In the present study we show for the first time a second pool of AIF in brain mitochondria and demonstrate that this pool does not require cleavage and that it contributes to the rapid release of AIF. Moreover, these results suggest that this outer mitochondrial pool of AIF is sufficient to cause cell death during parthanatos. Interfering with the release of this outer mitochondrial pool of AIF during cell injury paradigms that use parthanatos hold particular promise for novel therapies to treat neurological disorders.https://doi.org/10.1042/AN20090046
collection DOAJ
language English
format Article
sources DOAJ
author Seong-Woon Yu
Yingfei Wang
Didrik S Frydenlund
Ole Petter Ottersen
Valina L Dawson
Ted M Dawson
spellingShingle Seong-Woon Yu
Yingfei Wang
Didrik S Frydenlund
Ole Petter Ottersen
Valina L Dawson
Ted M Dawson
Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release
ASN Neuro
author_facet Seong-Woon Yu
Yingfei Wang
Didrik S Frydenlund
Ole Petter Ottersen
Valina L Dawson
Ted M Dawson
author_sort Seong-Woon Yu
title Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release
title_short Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release
title_full Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release
title_fullStr Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release
title_full_unstemmed Outer Mitochondrial Membrane Localization of Apoptosis-Inducing Factor: Mechanistic Implications for Release
title_sort outer mitochondrial membrane localization of apoptosis-inducing factor: mechanistic implications for release
publisher SAGE Publishing
series ASN Neuro
issn 1759-0914
1759-9091
publishDate 2009-10-01
description Poly(ADP-ribose) polymerase-1-dependent cell death (known as parthanatos) plays a pivotal role in many clinically important events including ischaemia/reperfusion injury and glutamate excitotoxicity. A recent study by us has shown that uncleaved AIF (apoptosis-inducing factor), but not calpain-hydrolysed truncated-AIF, was rapidly released from the mitochondria during parthanatos, implicating a second pool of AIF that might be present in brain mitochondria contributing to the rapid release. In the present study, a novel AIF pool is revealed in brain mitochondria by multiple biochemical analyses. Approx. 30% of AIF loosely associates with the outer mitochondrial membrane on the cytosolic side, in addition to its main localization in the mitochondrial intermembrane space attached to the inner membrane. Immunogold electron microscopic analysis of mouse brain further supports AIF association with the outer, as well as the inner, mitochondrial membrane in vivo . In line with these observations, approx. 20% of uncleaved AIF rapidly translocates to the nucleus and functionally causes neuronal death upon NMDA ( N -methyl- d -aspartate) treatment. In the present study we show for the first time a second pool of AIF in brain mitochondria and demonstrate that this pool does not require cleavage and that it contributes to the rapid release of AIF. Moreover, these results suggest that this outer mitochondrial pool of AIF is sufficient to cause cell death during parthanatos. Interfering with the release of this outer mitochondrial pool of AIF during cell injury paradigms that use parthanatos hold particular promise for novel therapies to treat neurological disorders.
url https://doi.org/10.1042/AN20090046
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