Therapeutic effect and potential mechanisms of intra-articular injections of miR-140-5p on early-stage osteoarthritis in rats

被引:12
作者
Cao, Fei [1 ,2 ,3 ]
Chen, Yang [4 ]
Wang, Xing [1 ,2 ]
Wu, Li-Min [1 ,2 ]
Tian, Mei [5 ]
Li, Han-Yu [6 ]
Si, Hai-Bo [1 ,2 ]
Shen, Bin [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Orthoped Res Inst, 37 Guoxue Rd, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Orthoped, 37 Guoxue Rd, Chengdu 610041, Peoples R China
[3] Chengdu First Peoples Hosp, Dept Orthoped, Chengdu 610041, Peoples R China
[4] Sichuan Univ, West China Hosp, Regenerat Med Res Ctr, Key Lab Transplant Engn & Immunol, Chengdu 610041, Peoples R China
[5] Sichuan Univ, West China Hosp, Dept Ultrasound, Chengdu 610041, Peoples R China
[6] Southwest Med Univ, Clin Med Tradit Chinese & Western Med, Luzhou 646000, Peoples R China
基金
中国国家自然科学基金;
关键词
Osteoarthritis; Cartilage; Chondrocytes; microRNA-140-5p; Intra-articular injections; CHONDROCYTES; CARTILAGE; DELIVERY; NOTCH; PROGRESSION; INHIBITION; ACID;
D O I
10.1016/j.intimp.2021.107786
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MicroRNAs (miRs) receive extensive attention in osteoarthritis (OA) pathogenesis in recent years, and our previous study confirmed that an intra-articular injection (IAJ) of miR-140-5p alleviates early-stage OA (EOA) progression in rats. This study aims to investigate the therapeutic effect and potential mechanisms of single IAJ (SIAJ) of miR-140-5p on different stage OA and multiple IAJs (MIAJ) of miR-140-5p on EOA. Firstly, the OA model was surgically induced in rats, nine were treated with IAJ of Cy5-miR-140-5p at one week after surgery, and fluorescence distribution was analyzed at different times. Then, 72 rats were treated with SIAJ of miR-1405p at different stages or MIAJ of miR-140-5p at one week after surgery, and OA progression was evaluated macroscopically and histologically at different times. Finally, the downstream targets and underlying molecular mechanisms of miR-140-5p were predicted by bioinformatics and partially validated. As a result, the intraarticularly injected miR-140-5p entered cartilage and could be taken up by chondrocytes rapidly. IAJ(s) of miR-140-5p improved the behavioral scores, chondrocyte number, cartilage thickness, and pathological scores to varying degrees. Specifically, the earlier a SIAJ of miR-140-5p was administrated, the better the therapeutic effect; meanwhile, MIAJ of miR-140-5p exhibited a better therapeutic effect than SIAJ on EOA. Eighty-four potential target genes and mechanisms of rno-miR-140-5p were predicted, and the effect of miR-140-5p on the potential target genes VEGFA and JAG1 was experimentally validated. Collectively, IAJs of miR-140-5p effectively alleviate EOA progression by modulating multiple biological processes and pathways in rats, representing a promising therapeutic for EOA.
引用
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页数:11
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