MiR-193b regulates early chondrogenesis by inhibiting the TGF-beta2 signaling pathway

被引:61
作者
Hou, Changhe [1 ]
Yang, Zibo [1 ]
Kang, Yan [1 ]
Zhang, Ziji [1 ]
Fu, Ming [1 ]
He, Aishan [1 ]
Zhang, Zhiqi [1 ]
Liao, Weiming [1 ]
机构
[1] Sun Yat Sen Univ, Joint Dept, Affiliated Hosp 1, Guangzhou 510080, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Chondrogenesis; Osteoarthritis; MiR-193b; TGF-beta; TNF-alpha; REPRESSES CELL-PROLIFERATION; GROWTH-FACTOR-BETA; CHONDROCYTE PROLIFERATION; STEM-CELLS; OSTEOGENIC DIFFERENTIATION; ARTICULAR-CARTILAGE; EXPRESSION; MICRORNAS; RUNX2; SOX9;
D O I
10.1016/j.febslet.2015.02.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cartilage generation and degradation are regulated by miRNAs. Our previous study has shown altered expression of miR-193b in chondrogenic human adipose-derived mesenchymal stem cells (hADSCs). In the current study, we investigated the role of miR-193b in chondrogenesis and cartilage degradation. Luciferase reporter assays showed that miR-193b targeted seed sequences of the TGFB2 and TGFBR3 3'-UTRs. MiR-193b suppressed the expression of early chondrogenic markers in chondrogenic ATDC5 cells, and TNF-alpha expression in IL-1b-induced PMCs. In conclusion, MiR-193b may inhibit early chondrogenesis by targeting TGFB2 and TGFBR3, and may regulate inflammation by repressing TNF-alpha expression in inflamed chondrocytes. (C) 2015 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:1040 / 1047
页数:8
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