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Invest Ophthalmol Vis Sci ; 57(8): 3723-30, 2016 07 01.
Article in English | MEDLINE | ID: mdl-27415790

ABSTRACT

PURPOSE: To identify the differently expressed micro (mi) RNAs in pterygium compared with normal conjunctiva and investigate the potential role of miRNAs in the pathogenesis of pterygium. METHODS: With microRNA microarray and quantitative RT-PCR, we identified that microRNA-122 (miR-122) was significantly decreased in pterygium tissue. We detected the expression of Bcl-w, a predicted target of miR-122, in both pterygium and normal conjunctiva, as well as its correlation with the expression of miR-122. Pterygium epithelial cells were isolated and cultured, and transfected with miR-122 mimic or miR-122 inhibitor to change the miR-122 levels. The regulation of Bcl-w expression by miR-122 was examined with luciferase activity assay, quantitative (q) RT-PCR, and Western blot. The effect of the miR-122 on the apoptosis of cultured pterygium epithelial cells was investigated with TUNEL staining and caspase activity assay. RESULTS: We found the expression of Bcl-w, with an inverse correlation with the expression of miR-122, was significantly increased in pterygium, especially in the superficial layer of epithelium. In cultured pterygium epithelial cells, miR-122 could specifically combine with Bcl-w mRNA, and negatively regulated the expression of Bcl-w. Suppression of miR-122 could reduce apoptosis and caspase activity in pterygium epithelial cell treated with TNFα/cycloheximide (CHX), and this effect was abolished by inhibition of the expression of Bcl-w with specific siRNA. CONCLUSIONS: Decreased expression of miR-122 in pterygium might result in abnormal cell apoptosis via its regulation of the expression of Bcl-w, and subsequently contribute to the development of pterygium.


Subject(s)
Apoptosis/physiology , MicroRNAs/physiology , Pterygium/etiology , Aged , Analysis of Variance , Apoptosis Regulatory Proteins/metabolism , Case-Control Studies , Caspases/metabolism , Cells, Cultured , Conjunctiva/metabolism , Cycloheximide/pharmacology , Down-Regulation/physiology , Epithelial Cells/metabolism , Humans , MicroRNAs/metabolism , Protein Synthesis Inhibitors/pharmacology , Tumor Necrosis Factor-alpha/pharmacology
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