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.
引用
收藏
页码:2897 / 2906
页数:10
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