期刊:Journal of Biomaterials and Tissue Engineering [American Scientific Publishers] 日期:2020-03-01卷期号:10 (3): 408-412
标识
DOI:10.1166/jbt.2020.2272
摘要
Inflammatory stress and angiogenesis participate in diabetic retinopathy. miR-199 α could inhibit the elevation of wound angiogenesis by suppressing TNF- α and NF-κB pathway. The mechanism of miR-199a in streptozotocin (STZ)-induced cell damage was assessed by ELLISA kit, western blotting, real-time RT-PCR. Reactive oxygen Species (ROS) was measured by flow cytometry. The over expression of miR-199a decreased the STZ-stimulated oxidative stress, inflammatory response, as well as VEGF expression. In conclusion, our results validated that overexpression of miR-199a protects RMECs from STZ-induced inflammation, oxidative stress and angiogenesis by targeting, at least partly, the VEGF signaling.