Inhibition of miR-449a Promotes Cartilage Regeneration and Prevents Progression of Osteoarthritis in In Vivo Rat Models

被引:37
作者
Baek, Dawoon [1 ,2 ]
Lee, Kyoung-Mi [1 ,3 ]
Park, Ki Won [1 ,2 ]
Suh, Jae Wan [5 ]
Choi, Seong Mi [1 ,2 ]
Park, Kwang Hwan [1 ]
Lee, Jin Woo [1 ,2 ,3 ]
Kim, Sung-Hwan [4 ]
机构
[1] Yonsei Univ, Coll Med, Dept Orthopaed Surg, 50-1 Yonsei Ro, Seoul 03722, South Korea
[2] Yonsei Univ, Coll Med, Brain Korea PLUS Project Med Sci 21, 50-1 Yonsei Ro, Seoul 03722, South Korea
[3] Yonsei Univ, Coll Med, Severance Biomed Sci Inst, 50-1 Yonsei Ro, Seoul 03722, South Korea
[4] Yonsei Univ, Coll Med, Gangnam Severance Hosp, Dept Orthopaed Surg, 211 Eonju Ro, Seoul 06273, South Korea
[5] Dankook Univ, Coll Med, Dankook Univ Hosp, Dept Orthopaed Surg, 201 Manghyang Ro, Cheonan 31116, South Korea
关键词
MESENCHYMAL STEM-CELLS; CHONDROGENIC DIFFERENTIATION; MICRORNA THERAPEUTICS; THERAPY; CANCER; CHONDROCYTES; REPAIR; TECHNOLOGY; EXPRESSION; DELIVERY;
D O I
10.1016/j.omtn.2018.09.015
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Traumatic and degenerative lesions of articular cartilage usually progress to osteoarthritis (OA), a leading cause of disability in humans. MicroRNAs (miRNAs) can regulate the differentiation of human bone marrow-derived mesenchymal stem cells (hBMSCs) and play important roles in the expression of genes related to OA. However, their functional roles in OA remain poorly understood. Here, we have examined miR-449a, which targets sirtuin 1 (SIRT1) and lymphoid enhancer-binding factor-1 (LEF-1), and observed its effects on damaged cartilage. The levels of chondrogenic markers and miR-449a target genes increased during chondrogenesis in anti-miR-449a-transfected hBMSCs. A locked nucleic acid (LNA)-anti-miR-449a increased cartilage regeneration and expression of type II collagen and aggrecan on the regenerated cartilage surface in acute defect and OA models. Furthermore, intra-articular injection of LNA-anti-miR-449a prevented disease progression in the OA model. Our study indicates that miR-449a may be a novel potential therapeutic target for age-related joint diseases like OA.
引用
收藏
页码:322 / 333
页数:12
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