TY - JOUR
T1 - Life with or without AIF
AU - Hangen, Emilie
AU - Blomgren, Klas
AU - Bénit, Paule
AU - Kroemer, Guido
AU - Modjtahedi, Nazanine
N1 - Funding Information:
We thank Pierre Rustin for his constructive critique. EH is supported by the Ligue Nationale contre le Cancer. GK is supported by the Ligue Nationale contre le Cancer (Equipes labellisée), Agence Nationale pour la Recherche (ANR), European Commission (Apo-Sys, ChemoRes, ApopTrain, Active p53), Fondation pour la Recherche Médicale (FRM), Institut National du Cancer (INCa) and Cancéropôle Ile-de-France. KB is supported by the Swedish Childhood Cancer Foundation (Barncancerfonden) and the Swedish Research Council. PB is supported by ANR, and the Association Française contre l’Ataxie de Friedreich (AFAF).
PY - 2010/1/1
Y1 - 2010/1/1
N2 - Apoptosis-inducing factor (AIF) was initially discovered as a caspase-independent death effector. AIF fulfills its lethal function after its release from mitochondria and its translocation to the nucleus of the dying cell. The contribution of AIF to programmed cell death is dependent upon the cell type and apoptotic insult. Recent in vivo data indicate that, in addition to its lethal activity, AIF plays a vital mitochondrial role in healthy cells. A segment of AIF which is dispensable for its apoptotic function carries an NADH-oxidase domain that regulates the respiratory chain complex I and is required for cell survival, proliferation and mitochondrial integrity. Mice that express reduced levels of AIF constitute a reliable model of complex I deficiency. Here we discuss recent reports on the survival-related function(s) of AIF.
AB - Apoptosis-inducing factor (AIF) was initially discovered as a caspase-independent death effector. AIF fulfills its lethal function after its release from mitochondria and its translocation to the nucleus of the dying cell. The contribution of AIF to programmed cell death is dependent upon the cell type and apoptotic insult. Recent in vivo data indicate that, in addition to its lethal activity, AIF plays a vital mitochondrial role in healthy cells. A segment of AIF which is dispensable for its apoptotic function carries an NADH-oxidase domain that regulates the respiratory chain complex I and is required for cell survival, proliferation and mitochondrial integrity. Mice that express reduced levels of AIF constitute a reliable model of complex I deficiency. Here we discuss recent reports on the survival-related function(s) of AIF.
UR - http://www.scopus.com/inward/record.url?scp=77952582542&partnerID=8YFLogxK
U2 - 10.1016/j.tibs.2009.12.008
DO - 10.1016/j.tibs.2009.12.008
M3 - Review article
AN - SCOPUS:77952582542
SN - 0968-0004
VL - 35
SP - 278
EP - 287
JO - Trends in Biochemical Sciences
JF - Trends in Biochemical Sciences
IS - 5
ER -