Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis

被引:21
作者
Ye, Liang [1 ]
Yu, Ting [1 ]
Li, Yanqun [1 ]
Chen, Bingni [1 ]
Zhang, Jinshun [1 ]
Wen, Zhongyang [1 ]
Zhang, Bo [1 ]
Zhou, Xiaohong [2 ]
Li, Xiaoqing [1 ]
Li, Feng [2 ]
Cao, Wei [2 ]
Huang, Zhong [1 ]
机构
[1] Shenzhen Univ, Sch Med, Inst Biotherapy, Shenzhen 518060, Guangdong, Peoples R China
[2] Univ Oklahoma, Hlth Sci Ctr, Dean A McGee Eye Inst, Dept Ophthalmol, Oklahoma City, OK 73104 USA
关键词
THIOREDOXIN-INTERACTING PROTEIN; ANTIOXIDANT-RESPONSIVE ELEMENT; PATHOGENESIS; DAMAGE; MOUSE; MODEL; NRF2; DEGENERATION; SULFIREDOXIN; INFLAMMATION;
D O I
10.1155/2013/413024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To gain further insights into the molecular basis of Sulforaphane (SF) mediated retinal pigment epithelial (RPE) 19 cell against oxidative stress, we investigated the effects of SF on the regulation of gene expression on a global scale and tested whether SF can endow RPE cells with the ability to resist apoptosis. The data revealed that after exposure to H2O2, RPE 19 cell viability was increased in the cells pretreated with SF compared to the cell not treated with SF. Microarray analysis revealed significant changes in the expression of 69 genes in RPE 19 cells after 6 hours of SF treatment. Based on the functional relevance, eight of the SF-responsive genes, that belong to antioxidant redox system, and inflammatory responsive factors were validated. The up-regulating translation of thioredoxin-1 (Trx1) and the nuclear translocation of Nuclear factor-like2 (Nrf2) were demonstrated by immunoblot analysis in SF treated RPE cells. Our data indicate that SF increases the ability of RPE 19 cell against oxidative stress through up-regulating antioxidative enzymes and down-regulating inflammatory mediators and chemokines. The results suggest that the antioxidant, SF, may be a valuable supplement for preventing and retarding the development of Age Related Macular Degeneration.
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页数:13
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