miR-210 promotes osteoblastic differentiation through inhibition of AcvR1b

被引:244
作者
Mizuno, Yosuke [2 ]
Tokuzawa, Yoshimi [2 ]
Ninomiya, Yuichi [2 ]
Yagi, Ken [2 ]
Yatsuka-Kanesaki, Yukiko [2 ]
Suda, Tatsuo [2 ]
Fukuda, Toru [3 ]
Katagiri, Takenobu [3 ]
Kondoh, Yasumitsu [4 ]
Amemiya, Tomoyuki [4 ]
Tashiro, Hideo [4 ]
Okazaki, Yasushi [1 ,2 ]
机构
[1] Saitama Med Univ, Res Ctr Genom Med, Div Translat Res, Hidaka 3501241, Japan
[2] Saitama Med Univ, Res Ctr Genom Med, Div Funct Genom & Syst Med, Hidaka 3501241, Japan
[3] Saitama Med Univ, Res Ctr Genom Med, Div Pathophysiol, Hidaka 3501241, Japan
[4] RIKEN, Probing Technol Lab, Wako, Saitama 3510198, Japan
关键词
miR-210; Differentiation; Osteoblast; Activin A receptor type 1B; MICRORNAS; SUPPRESSOR; PROLIFERATION; ONCOGENES; REPRESSES; TARGETS; HYPOXIA;
D O I
10.1016/j.febslet.2009.06.006
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
Although microRNAs (miRNAs) are involved in many biological processes, the mechanisms whereby miRNAs regulate osteoblastic differentiation are poorly understood. Here, we found that BMP-4-induced osteoblastic differentiation of bone marrow-derived ST2 stromal cells was promoted and repressed after transfection of sense and antisense miR-210, respectively. A reporter assay demonstrated that the activin A receptor type 1B (AcvR1b) gene was a target for miR-210. Furthermore, inhibition of transforming growth factor-beta (TGF-beta)/activin signaling in ST2 cells with SB431542 promoted osteoblastic differentiation. We conclude that miR-210 acts as a positive regulator of osteoblastic differentiation by inhibiting the TGF-beta/activin signaling pathway through inhibition of AcvR1b. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:2263 / 2268
页数:6
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