Proteomic analysis of rat retina in a steroid-induced ocular hypertension model: Potential vulnerability to oxidative stress

被引:45
作者
Miyara, Nariko [1 ,2 ]
Shinzato, Manabu [1 ,2 ]
Yamashiro, Yoshito [1 ]
Iwamatsu, Akihiro [3 ]
Kariya, Ken-ichi [1 ]
Sawaguchi, Shoichi [2 ]
机构
[1] Univ Ryukyus, Grad Sch Med, Div Cell Biol, Nishihara, Okinawa 9030215, Japan
[2] Univ Ryukyus, Dept Ophthalmol & Visual Sci, Sch Med, Okinawa, Japan
[3] Prot Res Network, Yokohama, Kanagawa, Japan
关键词
glucocorticoid; ocular hypertension; proteomics; retina;
D O I
10.1007/s10384-007-0507-5
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To investigate global protein expression profiles in the retinas of normal and glucocorticoid-induced ocular hypertensive rats by proteomic analysis. Methods: Ocular hypertension was induced by topical application of dexamethasone (DEX) for 4 weeks. Age-matched untreated rats served as controls. Intraocular pressure (IOP) was monitored by an electronic tonometer. Retinal protein expression profiling was carried out by two-dimensional fluorescence difference gel electrophoresis (2-D DIGE). Proteins were identified by matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry. Results: In DEX-treated rats, average IOP was elevated significantly compared with controls. With DEX treatment, levels of four proteins were altered, as revealed by 2-D DIGE and MALDI-TOF mass spectrometry: apolipoprotein A1 (apoA1), a lipid-binding protein, upregulated 1.9-fold, P < 0.05; alpha A crystallin (CRYAA), a molecular chaperone, downregulated 2.7-fold, P < 0.01; superoxide dismutase 1 (SOD1), an antioxidant enzyme, downregulated 2.3-fold, P < 0.05; and triosephosphate isomerase 1 (TPI1), a glycolytic enzyme, downregulated 2.3-fold, P < 0.01. Conclusions: Downregulation of CRYAA, SOD1, and TPI1, observed here after a short period of DEX-induced ocular hypertension, may be involved in the onset of neural damage in steroid-induced glaucoma.
引用
收藏
页码:84 / 90
页数:7
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