| Literature DB >> 25349431 |
Younghee Kim1, Valeria Tarallo2, Nagaraj Kerur1, Tetsuhiro Yasuma1, Bradley D Gelfand3, Ana Bastos-Carvalho1, Yoshio Hirano1, Reo Yasuma1, Takeshi Mizutani1, Benjamin J Fowler4, Shengjian Li1, Hiroki Kaneko1, Sasha Bogdanovich1, Balamurali K Ambati5, David R Hinton6, William W Hauswirth7, Razqallah Hakem8, Charles Wright1, Jayakrishna Ambati9.
Abstract
Geographic atrophy, an advanced form of age-related macular degeneration (AMD) characterized by death of the retinal pigmented epithelium (RPE), causes untreatable blindness in millions worldwide. The RPE of human eyes with geographic atrophy accumulates toxic Alu RNA in response to a deficit in the enzyme DICER1, which in turn leads to activation of the NLRP3 inflammasome and elaboration of IL-18. Despite these recent insights, it is still unclear how RPE cells die during the course of the disease. In this study, we implicate the involvement of Caspase-8 as a critical mediator of RPE degeneration. Here we show that DICER1 deficiency, Alu RNA accumulation, and IL-18 up-regulation lead to RPE cell death via activation of Caspase-8 through a Fas ligand-dependent mechanism. Coupled with our observation of increased Caspase-8 expression in the RPE of human eyes with geographic atrophy, our findings provide a rationale for targeting this apoptotic pathway in this disease.Entities:
Keywords: caspase; inflammasome; macular degeneration
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Year: 2014 PMID: 25349431 PMCID: PMC4234570 DOI: 10.1073/pnas.1403814111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205