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Interleukin 27 Induces the Expression of Complement Factor H (CFH) in the Retina
被引:25
|作者:
Amadi-Obi, Ahjoku
[1
]
Yu, Cheng-Rong
[1
]
Dambuza, Ivy
[1
]
Kim, Sung-Hye
[1
]
Marrero, Bernadette
[1
]
Egwuagu, Charles E.
[1
]
机构:
[1] NEI, Mol Immunol Sect, NIH, Bethesda, MD 20892 USA
来源:
基金:
美国国家卫生研究院;
关键词:
TRANSCRIPTION FACTORS;
MACULAR DEGENERATION;
EPITHELIAL-CELLS;
B-CELL;
INFLAMMATION;
UVEITIS;
CYTOKINE;
REGION;
IRF8;
PATHOGENESIS;
D O I:
10.1371/journal.pone.0045801
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Complement factor H (CFH) is a central regulator of the complement system and has been implicated in the etiology of age-related macular degeneration (AMD), a leading cause of blindness in the elderly. In view of previous studies showing that reduced expression of CFH in the retina is a risk factor for developing AMD, there is significant interest in understanding how CFH expression is regulated in the retina. In this study, we have shown that the anti-inflammatory cytokine, IL-27, induced CFH expression in mouse retinal cells and human retinal pigmented epithelial cells (RPE) through STAT1-mediated up-regulation of Interferon Regulatory Factor-1 (IRF-1) and IRF-8. We further show that cells in the ganglion and inner-nuclear layers of the retina constitutively express IRF-1 and IRF-8 and enhanced CFH expression in the retina during ocular inflammation correlated with significant increase in the expression of IRF-1, IRF-8 and IL-27 (IL-27p28 and Ebi3). Our data thus reveal a novel role of IL-27 in regulating complement activation through up-regulation of CFH and suggest that defects in IL-27 signaling or expression may contribute to the reduction of CFH expression in the retina of patients with AMD.
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页数:9
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