4.3 Article

MicroRNA-1 26 Reduces Blood-Retina Barrier Breakdown via the Regulation of VCAM-1 and BCL2L11 in Ischemic Retinopathy

期刊

OPHTHALMIC RESEARCH
卷 57, 期 3, 页码 173-185

出版社

KARGER
DOI: 10.1159/000454716

关键词

MicroRNA-126; Vascular cell adhesion molecule 1; BCL2L11; Blood-retina barrier; Tight junction; Ischemic retinopathy

资金

  1. National Natural Science Foundation of China [81200698]
  2. Jiangsu Provincial Natural Science Foundation in China [BK2012626]
  3. Natural Science Foundation of Jiangsu Provincial Department of Education in China [12KJB310014]
  4. iangsu Overseas Research and Training

向作者/读者索取更多资源

To evaluate the role of microRNA-126 (miR-126) in maintaining the integrity of the blood-retina barrier (BRB), we established a mouse model of oxygen-induced retinopathy (OIR) and measured the retinal levels of miR-126 using recombinant plasmid pCMV-MIR or pCMV-MIR-126 intravitreal injections. We also detected VCAM-1 and BCL2L11 levels. Retinal vaso-obliteration,VCAM-1 localization on retinal endothelial cells, the blood-retina vascular permeability or albumin leakage in retinas, TUNEL histology, Evans blue assays, or Western blotting for detecting albumin or tight junction levels in the retina was performed. We also detected the effect of miR-126 on the survival of Muller cells in a mouse model using vimentin fluorescence staining. Our results suggested that miR-126 may not only regulate the overexpression of VCAM-1 or BCL2L11 and lead to the reduction of retinal endothelial cell apoptosis, retinal vascular leakage, or retinalpermeability in the OIR mouse model, but may also protect hypoxic retinal Muller cells via the STAT3 signaling pathway. We believe that miR-126 could also be a potential therapeutic agent to maintain the stability of the BRB in ischemic retinopathy. (C) 2017 S. Ka rger AG, Basel

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