Mechanism of piR-1245/PIWI-like protein-2 regulating Janus kinase-2/signal transducer and activator of transcription-3/vascular endothelial growth factor signaling pathway in retinal neovascularization

被引:5
作者
Yu, Yong [1 ]
Xia, Li-Kun [1 ]
Di, Yu [1 ]
Nie, Qing-Zhu [1 ]
Chen, Xiao-Long [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Ophthalmol, Shenyang, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
angiogenesis; human retinal endothelial cells; hypoxia inducible factor-1 alpha; hypoxia; interleukin-1; beta; migration; non-coding RNA; oxygen-induced injury; PIWI-interacting RNA; retinopathy; PIWI-INTERACTING RNAS; EXPRESSION; NANOPARTICLES; JAK2/STAT3; CANCER; IMAGE;
D O I
10.4103/1673-5374.355819
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inhibiting retinal neovascularization is the optimal strategy for the treatment of retina-related diseases, but there is currently no effective treatment for retinal neovascularization. P-element-induced wimpy testis (PIWI)-interacting RNA (piRNA) is a type of small non-coding RNA implicated in a variety of diseases. In this study, we found that the expression of piR-1245 and the interacting protein PIWIL2 were remarkably increased in human retinal endothelial cells cultured in a hypoxic environment, and cell apoptosis, migration, tube formation and proliferation were remarkably enhanced in these cells. Knocking down piR-1245 inhibited the above phenomena. After intervention by a p-JAK2 activator, piR-1245 decreased the expression of hypoxia inducible factor-1 alpha and vascular endothelial growth factor through the JAK2/STAT3 pathway. For in vivo analysis, 7-day-old newborn mice were raised in 75 +/- 2% hyperoxia for 5 days and then piR-1245 in the retina was knocked down. In these mice, the number of newly formed vessels in the retina was decreased, the expressions of inflammation-related proteins were reduced, the number of apoptotic cells in the retina was decreased, the JAK2/STAT3 pathway was inhibited, and the expressions of hypoxia inducible factor-1 alpha and vascular endothelial growth factor were decreased. Injection of the JAK2 inhibitor JAK2/TYK2-IN-1 into the vitreous cavity inhibited retinal neovascularization in mice and reduced expression of hypoxia inducible factor-1 alpha and vascular endothelial growth factor. These findings suggest that piR-1245 activates the JAK2/STAT3 pathway, regulates the expression of hypoxia inducible factor-1 alpha and vascular endothelial growth factor, and promotes retinal neovascularization. Therefore, piR-1245 may be a new therapeutic target for retinal neovascularization.
引用
收藏
页码:1132 / 1138
页数:7
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