| Literature DB >> 29409883 |
Yun-Xi Zhu1, Jin Yao1, Chang Liu2, Hai-Tao Hu1, Xiu-Miao Li3, Hui-Min Ge4, Yun-Fan Zhou4, Kun Shan5, Qin Jiang6, Biao Yan7.
Abstract
Excessive light exposure leads to retinal degeneration and accelerates the progression and severity of several ocular diseases, such as age-related macular degeneration (AMD) and retinitis pigmentosa. Long non-coding RNAs (LncRNAs) have emerged as important regulators of photoreceptor development and ocular diseases. In this study, we investigated the role of lncRNA-MEG3 in light-induced retinal degeneration. MEG3 expression was significantly up-regulated after light insult in vivo and in vitro. MEG3 silencing protected against light-induced retinal degeneration in vivo and light-induced photoreceptor cell apoptosis in vitro. Mechanistically, MEG3 regulated retinal photoreceptor cell function by acting as p53 decoy. MEG3 silencing decreased caspase 3/7 activity, up-regulated anti-apoptotic protein (Bcl-2) expression, and down-regulated pro-apoptotic protein (Bax) expression. Taken together, this study provides a promising method of MEG3 silencing for treating light-induced retinal degeneration.Entities:
Keywords: Light insult; Long non-coding RNA; Protein decoy; Retinal degeneration
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Year: 2018 PMID: 29409883 DOI: 10.1016/j.bbrc.2018.01.177
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575