A microRNA regulatory mechanism of osteoblast differentiation

被引:251
作者
Inose, Hiroyuki [1 ]
Ochi, Hiroki [4 ]
Kimura, Ayako [1 ,2 ]
Fujita, Koji [1 ,2 ]
Xu, Ren [1 ]
Sato, Shingo [1 ]
Iwasaki, Makiko [1 ]
Sunamura, Satoko [7 ]
Takeuchi, Yasuhiro [5 ]
Fukumoto, Seiji [6 ]
Saito, Kuniaki [8 ]
Nakamura, Takashi [3 ]
Siomi, Haruhiko [8 ]
Ito, Hiroshi [7 ]
Arai, Yoshiyasu [1 ]
Shinomiya, Ken-ichi [1 ,2 ]
Takeda, Shu [1 ,7 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Dept Orthoped, Bunkyo Ku, Tokyo 1138519, Japan
[2] Tokyo Med & Dent Univ, Global Ctr Excellence Program, Bunkyo Ku, Tokyo 1138519, Japan
[3] Tokyo Med & Dent Univ, Dept Dev & Regenerat Biol, Bunkyo Ku, Tokyo 1138519, Japan
[4] Nippon Vet & Life Sci Univ, Fac Vet Med, Dept Vet Sci, Musashino, Tokyo 1808602, Japan
[5] Toranomon Gen Hosp, Endocrine Ctr, Minato Ku, Tokyo 1058470, Japan
[6] Tokyo Univ Hosp, Dept Internal Med, Div Nephrol & Endocrinol, Bunkyo Ku, Tokyo 1138655, Japan
[7] Keio Univ, Sch Med, Dept Internal Med, Sect Nephrol Endocrinol & Metab,Shinjuku Ku, Tokyo 1608582, Japan
[8] Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan
基金
日本学术振兴会;
关键词
Connexin43; miR-206; MUSCLE-SPECIFIC MICRORNAS; PARATHYROID-HORMONE; NONCODING RNAS; MESSENGER-RNA; EXPRESSION; TRANSCRIPTION; BONE; PROMOTER; MIR-206; REGIONS;
D O I
10.1073/pnas.0909311106
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
07 ; 0710 ; 09 ;
摘要
Growing evidence shows that microRNAs (miRNAs) regulate various developmental and homeostatic events in vertebrates and invertebrates. Osteoblast differentiation is a key step in proper skeletal development and acquisition of bone mass; however, the physiological role of non-coding small RNAs, especially miRNAs, in osteoblast differentiation remains elusive. Here, through comprehensive analysis of miRNAs expression during osteoblast differentiation, we show that miR-206, previously viewed as a musclespecific miRNA, is a key regulator of this process. miR-206 was expressed in osteoblasts, and its expression decreased over the course of osteoblast differentiation. Overexpression of miR-206 in osteoblasts inhibited their differentiation, and conversely, knockdown of miR-206 expression promoted osteoblast differentiation. In silico analysis and molecular experiments revealed connexin 43 (Cx43), a major gap junction protein in osteoblasts, as a target of miR-206, and restoration of Cx43 expression in miR-206-expressing osteoblasts rescued them from the inhibitory effect of miR-206 on osteoblast differentiation. Finally, transgenic mice expressing miR-206 in osteoblasts developed a low bone mass phenotype due to impaired osteoblast differentiation. Our data show that miRNA is a regulator of osteoblast differentiation.
引用
收藏
页码:20794 / 20799
页数:6
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