共 84 条
Mitochondrial DNA has a pro-inflammatory role in AMD
被引:51
作者:
Dib, Bernard
[1
]
Lin, Haijiang
[1
]
Maidana, Daniel E.
[1
]
Tian, Bo
[1
]
Miller, John B.
[1
]
Bouzika, Peggy
[1
]
Miller, Joan W.
[1
]
Vavvas, Demetrios G.
[1
]
机构:
[1] Harvard Univ, Sch Med, Massachusetts Eye & Ear Infirm, Dept Ophthalmol,Retina Serv,Angiogenesis Lab, Boston, MA 02114 USA
来源:
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
|
2015年
/
1853卷
/
11期
关键词:
Age-related macular degeneration;
Retinal pigment epithelium;
Mitochondrial DNA;
Inflammation;
NLRP3;
inflammasome;
NF-KAPPA-B;
RETINAL-PIGMENT EPITHELIUM;
ENDOTHELIAL GROWTH-FACTOR;
MACULAR DEGENERATION;
NLRP3;
INFLAMMASOME;
CHOROIDAL NEOVASCULARIZATION;
OXIDATIVE STRESS;
ARPE-19;
CELLS;
MALATTIA LEVENTINESE;
AQUEOUS-HUMOR;
D O I:
10.1016/j.bbamcr.2015.08.012
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in the elderly of industrialized nations, and there is increasing evidence to support a role for chronic inflammation in its pathogenesis. Mitochondrial DNA (mtDNA) has been recently reported to be pro-inflammatory in various diseases such as Alzheimer's and heart failure. Here, we report that intracellular mtDNA induces ARPE-19 cells to secrete inflammatory cytokines IL-6 and IL-8, which have been consistently associated with AMD onset and progression. The induction was dependent on the size of mtDNA, but not on specific sequence. Oxidative stress plays a major role in the development of AMD, and our findings indicate that mtDNA induces IL-6 and IL-8 more potently when oxidized. Cytokine induction was mediated by STING (Stimulator of Interferon Genes) and NF-kappa B as evidenced by abrogation of the cytokine response with the use of specific inhibitors (siRNA and BAY 11-7082, respectively). Finally, mtDNA primed the NLRP3 inflammasome. This study contributes to our understanding of the potential pro-inflammatory role of mtDNA in the pathogenesis of AMD. (C) 2015 Elsevier B.V. All rights reserved.
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页码:2897 / 2906
页数:10
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