细胞凋亡
流式细胞术
类风湿性关节炎
细胞周期
免疫印迹
小RNA
癌症研究
细胞生长
成纤维细胞
关节炎
免疫学
化学
医学
生物
细胞培养
基因
生物化学
遗传学
作者
Aixian Zhang,Rong Lü,Huifang Lang,Min Wu
出处
期刊:Autoimmunity
[Informa]
日期:2022-05-24
卷期号:55 (5): 310-317
被引量:6
标识
DOI:10.1080/08916934.2022.2073588
摘要
This study is aimed to explore the key role of miR-361-5p in fibroblast-like synovial (FLS) cells of rheumatoid arthritis (RA) and explore the underlying mechanism.First, we performed RT-qPCR to evaluate the expression of miR-361-5p in both synovial tissues of RA patients and cultured RA-FLS cells. Then CCK-8 assay, EdU staining, Western blot, flow cytometry, and ELISA were conducted to estimate the influence of inhibiting miR-361-5p on RA-FLS cells. Moreover, we used bioinformatics analysis to predict the potential targets of miR-361-5p and perform a dual luciferase report assay for verification. Finally, rescue experiments were performed to prove the role of miR-361-5p/Zinc Finger And BTB Domain Containing 10 (ZBTB10) in the proliferation, cell cycle, and apoptosis of RA-FLS.We find that the expression of miR-361-5p is increased in both RA tissues and cultured RA-FLS cells. The inhibition of miR-361-5p can not only inhibit proliferation, arrest the cell cycle in G1/G0 phase, and increase apoptosis, but also reduce the inflammatory factors secreted by RA-FLS cells. In addition, ZBTB10 is a direct target for miR-361-5p, over-expression of ZBTB10 reverses the effect of miR-361-5p in RA-FLS.MiR-361-5p promotes the progression of rheumatoid arthritis by targeting ZBTB10.Key pointsThe influences of miR-361-5p on RA-FLS cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI