Overexpression of microRNA-634 suppresses survival and matrix synthesis of human osteoarthritis chondrocytes by targeting PIK3R1

被引:56
作者
Cui, Xu [1 ]
Wang, Shaojie [1 ]
Cai, Heguo [1 ]
Lin, Yuan [1 ]
Zheng, Xinpeng [1 ]
Zhang, Bing [2 ]
Xia, Chun [1 ]
机构
[1] Xiamen Univ, Zhongshan Hosp, Xiamen 361000, Fujian, Peoples R China
[2] Xiamen Univ, Sch Med, Xiamen 361102, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
PROTEIN-KINASE B; GROWTH-FACTOR; CARTILAGE DEGENERATION; RAT MODEL; APOPTOSIS; EXPRESSION; IDENTIFICATION; PATHWAYS; PHOSPHORYLATION; PROLIFERATION;
D O I
10.1038/srep23117
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Osteoarthritis (OA) is a degenerative disease characterized by deterioration of articular cartilage. Recent studies have demonstrated the importance of some microRNAs in cartilage damage. The aim of this study was to identify and characterize the expression of microRNA-634 (miR-634) in normal and OA chondrocytes, and to determine its role in OA pathogenesis. Human normal and OA chondrocytes obtained from patients were cultured in vitro. Transfection with miR-634 mimic or inhibitor was employed to investigate the effect of miR-634 on chondrocyte survival and matrix synthesis, and to identify miR-634 target. The results indicated that miR-634 was expressed at lower level in high grade OA chondrocyte compared with normal chondrocytes. Overexpression of miR-634 could inhibit cell survival and matrix synthesis in high grade OA chondrocytes. Furthermore, miR-634 targeted PIK3R1 gene that encodes the regulatory subunit 1 of class I PI3K (p85 alpha) and exerted its inhibitory effect on the phosphorylation of Akt, mTOR, and S6 signal molecules in high grade OA chondrocytes. Therefore, the data suggested that miR-634 could suppress survival and matrix synthesis of high grade OA chondrocytes through targeting PIK3R1 gene to modulate the PI3K/Akt/S6 and PI3K/Akt/mTOR/S6 axes, with important implication for validating miR-634 as a potential target for OA therapy.
引用
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页数:11
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