TY - JOUR
T1 - Relocalization of apoptosis-inducing factor in photoreceptor apoptosis induced by retinal detachment in vivo
AU - Hisatomi, Toshio
AU - Sakamoto, Taiji
AU - Murata, Toshinori
AU - Yamanaka, Ichiro
AU - Oshima, Yuji
AU - Hata, Yasuaki
AU - Ishibashi, Tatsuro
AU - Inomata, Hajime
AU - Susin, Santos A.
AU - Kroemer, Guido
N1 - Funding Information:
We thank Dr. Kenneth W. Parker for editorial assistance, and Drs. Shozo Shimokawa, Masao Uehara, and Hiroki Sanui for financial support.
PY - 2001/1/1
Y1 - 2001/1/1
N2 - Apoptosis-inducing factor (AIF) is a novel mediator in apoptosis. AIF is a flavoprotein that is normally confined to the mitochondrial intermembrane space, yet translocates to the nucleus in several in vitro models of apoptosis. To investigate the role of AIF in the apoptotic process in vivo, we induced retinal detachment (RD) by subretinal injection of sodium hyaluronate, either in Brown Norway rats or in C3H mice. Apoptotic DNA fragmentation, as determined by terminal nick-end labeling, was most prominent 3 days after RD. The subcellular localization of AIF was examined by immunohistochemistry and immunoelectron microscopy. In normal photoreceptor cells, AIF was present in the mitochondrion-rich inner segment. However, AIF was found in the nucleus after RD. Photoreceptor apoptosis developed similarly in C3H control mice, and in mice bearing the gld or lpr mutations, indicating that cell death occurs independently from the CD95/CD95 ligand system. Both the mitochondrio-nuclear transition of AIF localization and the nuclear DNA fragmentation were inhibited by subretinal application of brain-derived neurotrophic factor. To our knowledge, this is the first description of AIF relocalization occurring in a clinically relevant, in vivo model of apoptosis.
AB - Apoptosis-inducing factor (AIF) is a novel mediator in apoptosis. AIF is a flavoprotein that is normally confined to the mitochondrial intermembrane space, yet translocates to the nucleus in several in vitro models of apoptosis. To investigate the role of AIF in the apoptotic process in vivo, we induced retinal detachment (RD) by subretinal injection of sodium hyaluronate, either in Brown Norway rats or in C3H mice. Apoptotic DNA fragmentation, as determined by terminal nick-end labeling, was most prominent 3 days after RD. The subcellular localization of AIF was examined by immunohistochemistry and immunoelectron microscopy. In normal photoreceptor cells, AIF was present in the mitochondrion-rich inner segment. However, AIF was found in the nucleus after RD. Photoreceptor apoptosis developed similarly in C3H control mice, and in mice bearing the gld or lpr mutations, indicating that cell death occurs independently from the CD95/CD95 ligand system. Both the mitochondrio-nuclear transition of AIF localization and the nuclear DNA fragmentation were inhibited by subretinal application of brain-derived neurotrophic factor. To our knowledge, this is the first description of AIF relocalization occurring in a clinically relevant, in vivo model of apoptosis.
UR - http://www.scopus.com/inward/record.url?scp=0035069843&partnerID=8YFLogxK
U2 - 10.1016/S0002-9440(10)64078-3
DO - 10.1016/S0002-9440(10)64078-3
M3 - Article
C2 - 11290545
AN - SCOPUS:0035069843
SN - 0002-9440
VL - 158
SP - 1271
EP - 1278
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 4
M1 - 64078
ER -