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2015 Fiscal Year Final Research Report

Involvement of programmed necrosis in age-related macular degeneration

Research Project

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Project/Area Number 25861637
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Ophthalmology
Research InstitutionKyushu University

Principal Investigator

Murakami Yusuke  九州大学, 大学病院, 助教 (50634995)

Research Collaborator VAVVAS Demetrios  
Project Period (FY) 2013-04-01 – 2016-03-31
Keywords加齢黄斑変性 / 能動的ネクローシス / RIPキナーゼ
Outline of Final Research Achievements

Double strand RNA (dsRNA) accumulates in the drusen of AMD patient eyes, and has been shown to be implicated in the development of the disease. Here we investigated the mechanisms by which dsRNA causes retinal degeneration in mice. Subretinal injection of dsRNA caused both apoptotic and necrotic photoreceptor cell death, while it mediated necrosis of the retinal pigment epithelium (RPE). These necrotic changes were substantially suppressed by RIP kinase inhibition. Thus, RIP kinase-mediated necrosis is crucial in dsRNA-induced retinal degeneration, and RIP kinase may be a novel therapeutic target for retinal degenerative diseases such as AMD.

Free Research Field

眼科学

URL: 

Published: 2017-05-10  

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