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环状 RNA-ZNF609 通过作为 miR-615 的海绵来调节视网膜神经退行性变。

Circular RNA-ZNF609 regulates retinal neurodegeneration by acting as miR-615 sponge.

机构信息

Eye Institute, Eye & ENT Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

The Fourth School of Clinical Medicine, Nanjing Medical University, Nanjing, China.

出版信息

Theranostics. 2018 May 24;8(12):3408-3415. doi: 10.7150/thno.25156. eCollection 2018.

DOI:10.7150/thno.25156
PMID:29930739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6010990/
Abstract

Glaucoma is a major cause of visual impairment characterized by progressive retinal neurodegeneration. Circular RNAs are a class of endogenous noncoding RNAs that regulate gene expression in eukaryotes. In this study, we investigated the role of cZNF609 in retinal neurodegeneration induced by glaucoma. qRT-PCR and Sanger sequencing were conducted to detect cZNF609 expression pattern during retinal neurodegeneration. Immunofluorescence staining was conducted to detect the effect of cZNF609 silencing on retinal neurodegeneration in vivo. MTT assay, Ki67 staining, and PI staining were conducted to detect the effect of cZNF609 silencing on retinal glial cells and RGC function in vitro. Bioinformatics analysis, RNA pull-down assays, and in vitro studies were conducted to reveal the mechanism of cZNF609-mediated retinal neurodegeneration. cZNF609 expression was significantly up-regulated during retinal neurodegeneration. cZNF609 silencing reduced retinal reactive gliosis and glial cell activation, and facilitated RGC survival in vivo. cZNF609 silencing directly regulated Müller cell function but indirectly regulated RGC function in vitro. cZNF609 acted as an endogenous miR-615 sponge to sequester and inhibit miR-615 activity, which led to increased METRN. METRN overexpression could partially rescue cZNF609 silencing-mediated inhibitory effects on retinal glial cell proliferation. Intervention of cZNF609 expression is a promising therapeutic strategy for retinal neurodegeneration.

摘要

青光眼是一种主要的视觉障碍疾病,其特征是视网膜神经退行性病变的进行性发展。环状 RNA 是一类内源性非编码 RNA,它们在真核生物中调节基因表达。在本研究中,我们研究了 cZNF609 在青光眼诱导的视网膜神经退行性变中的作用。qRT-PCR 和 Sanger 测序用于检测 cZNF609 在视网膜神经退行性变过程中的表达模式。免疫荧光染色用于检测 cZNF609 沉默对体内视网膜神经退行性变的影响。MTT 测定、Ki67 染色和 PI 染色用于检测 cZNF609 沉默对体外视网膜神经胶质细胞和 RGC 功能的影响。生物信息学分析、RNA 下拉实验和体外研究用于揭示 cZNF609 介导的视网膜神经退行性变的机制。cZNF609 的表达在视网膜神经退行性变过程中显著上调。cZNF609 沉默减少了视网膜反应性胶质增生和胶质细胞激活,并促进了体内 RGC 的存活。cZNF609 沉默在体外直接调节 Muller 细胞功能,但间接调节 RGC 功能。cZNF609 作为内源性 miR-615 海绵,可结合并抑制 miR-615 的活性,从而导致 METRN 的增加。METRN 的过表达可以部分挽救 cZNF609 沉默介导的对视网膜神经胶质细胞增殖的抑制作用。干预 cZNF609 的表达是治疗视网膜神经退行性变的一种有前途的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bd/6010990/d58a8ae3b256/thnov08p3408g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bd/6010990/830837f3e125/thnov08p3408g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bd/6010990/d58a8ae3b256/thnov08p3408g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bd/6010990/b1175ef06bf6/thnov08p3408g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bd/6010990/e7b5e14e8071/thnov08p3408g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bd/6010990/a1962aa0c925/thnov08p3408g003.jpg
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