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体内视网膜脱离诱导的光感受器细胞凋亡中凋亡诱导因子的重新定位

Relocalization of apoptosis-inducing factor in photoreceptor apoptosis induced by retinal detachment in vivo.

作者信息

Hisatomi T, Sakamoto T, Murata T, Yamanaka I, Oshima Y, Hata Y, Ishibashi T, Inomata H, Susin S A, Kroemer G

机构信息

Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

出版信息

Am J Pathol. 2001 Apr;158(4):1271-8. doi: 10.1016/S0002-9440(10)64078-3.

Abstract

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.

摘要

凋亡诱导因子(AIF)是细胞凋亡中的一种新型介质。AIF是一种黄素蛋白,通常局限于线粒体内膜间隙,但在几种细胞凋亡的体外模型中会转移至细胞核。为了研究AIF在体内凋亡过程中的作用,我们通过在棕色挪威大鼠或C3H小鼠的视网膜下注射透明质酸钠诱导视网膜脱离(RD)。通过末端缺口末端标记法测定,凋亡DNA片段化在RD后3天最为明显。通过免疫组织化学和免疫电子显微镜检查AIF的亚细胞定位。在正常的光感受器细胞中,AIF存在于富含线粒体的内段。然而,RD后在细胞核中发现了AIF。在C3H对照小鼠以及携带gld或lpr突变的小鼠中,光感受器凋亡的发展情况相似,这表明细胞死亡独立于CD95/CD95配体系统发生。视网膜下应用脑源性神经营养因子可抑制AIF定位的线粒体-核转变以及核DNA片段化。据我们所知,这是首次在临床相关的体内细胞凋亡模型中描述AIF重新定位的情况。

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本文引用的文献

1
Mitochondrial control of cell death.细胞死亡的线粒体调控
Nat Med. 2000 May;6(5):513-9. doi: 10.1038/74994.

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