Endoplasmic reticulum stress is activated in light-induced retinal degeneration

被引:45
作者
Yang, Li-ping [1 ]
Wu, Le-meng [1 ]
Guo, Xiu-juan [1 ]
Li, Ying [1 ]
Tso, Mark O. M. [1 ,2 ]
机构
[1] Peking Univ, Peking Univ Hosp 3, Peking Univ Eye Ctr, Beijing 100083, Peoples R China
[2] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA
关键词
apoptosis; unfolded protein response; GRP78/BiP; caspase-12; eIf2; alpha; PERK;
D O I
10.1002/jnr.21535
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Exposure to excessive levels of light induces photoreceptor apoptosis and has previously been used as a model for the study of retinal degeneration. During the light exposure, intracellular calcium levels increase, and reactive oxygen species (ROS) are generated, which have been shown to cause endoplasmic reticulum (ER) stress. In the present study, we investigated the role of ER stress in light-induced photoreceptor apoptosis. Our study demonstrated that, after light exposure, the ER stress sensors including glucose-regulated protein-78 (GRP78/BiP), caspase-12, phospho-eukaryotic initiation factor 2 alpha (eIF2 alpha), and phospho-pancreatic ER kinase (PERK) were significantly up-regulated in a time-dependent manner. The up-regulation of these proteins coincided with or preceded the photoreceptor apoptosis indicated by TUNEL. These data showed that ER stress played an important role in light-induced photoreceptor apoptosis. Therefore, ER stress modulators could be strong candidates as therapeutic agents in the treatment of retinal degenerative diseases. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:910 / 919
页数:10
相关论文
共 37 条
[1]   Endoplasmic reticulum of animal cells and its organization into structural and functional domains [J].
Baumann, O ;
Walz, B .
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 205, 2001, 205 :149-214
[2]   ER stress-regulated translation increases tolerance to extreme hypoxia and promotes tumor growth [J].
Bi, MX ;
Naczki, C ;
Koritzinsky, M ;
Fels, D ;
Blais, J ;
Hu, NP ;
Harding, H ;
Novoa, I ;
Varia, M ;
Raleigh, J ;
Scheuner, D ;
Kaufman, RJ ;
Bell, J ;
Ron, D ;
Wouters, BG ;
Koumenis, C .
EMBO JOURNAL, 2005, 24 (19) :3470-3481
[3]   Cellular response to endoplasmic reticulum stress: a matter of life or death [J].
Boyce, M ;
Yuan, J .
CELL DEATH AND DIFFERENTIATION, 2006, 13 (03) :363-373
[4]   Oxidative stress induces caspase-independent retinal apoptosis in vitro [J].
Carmody, RJ ;
Cotter, TG .
CELL DEATH AND DIFFERENTIATION, 2000, 7 (03) :282-291
[5]   APOPTOSIS - FINAL COMMON PATHWAY OF PHOTORECEPTOR DEATH IN RD, RDS, AND RHODOPSIN MUTANT MICE [J].
CHANG, GQ ;
HAO, Y ;
WONG, F .
NEURON, 1993, 11 (04) :595-605
[6]   DEFECTIVE INTRACELLULAR-TRANSPORT IS THE MOLECULAR-BASIS OF RHODOPSIN-DEPENDENT DOMINANT RETINAL DEGENERATION [J].
COLLEY, NJ ;
CASSILL, JA ;
BAKER, EK ;
ZUKER, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :3070-3074
[7]   Caspase-independent photoreceptor apoptosis in vivo and differential expression of apoptotic protease activating factor-1 and caspase-3 during retinal development [J].
Donovan, M ;
Cotter, TG .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (11) :1220-1231
[8]   Light-induced photoreceptor apoptosis in vivo requires neuronal nitric-oxide synthase and guanylate cyclase activity and is caspase-3 independent [J].
Donovan, M ;
Carmody, RJ ;
Cotter, TG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (25) :23000-23008
[9]   Caspase-12 processing and fragment translocation into nuclei of tunicamycin-treated cells [J].
Fujita, E ;
Kouroku, Y ;
Jimbo, A ;
Isoai, A ;
Maruyama, K ;
Momoi, T .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (10) :1108-1114
[10]   Evidence for two apoptotic pathways in light-induced retinal degeneration [J].
Hao, WS ;
Wenzel, A ;
Obin, MS ;
Chen, CK ;
Brill, E ;
Krasnoperova, NV ;
Eversole-Cire, P ;
Kleyner, Y ;
Taylor, A ;
Simon, MI ;
Grimm, C ;
Remé, C ;
Remé, CE ;
Lem, J .
NATURE GENETICS, 2002, 32 (02) :254-260