Role of miR-17 Family in the Negative Feedback Loop of Bone Morphogenetic Protein Signaling in Neuron

被引:21
|
作者
Sun, Qi [1 ]
Mao, Susu [1 ]
Li, Hanqin [1 ]
Zen, Ke [1 ,2 ]
Zhang, Chen-Yu [1 ]
Li, Liang [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Jiangsu Engn Res Ctr MicroRNA Biol & Biotechnol, Nanjing 210008, Jiangsu, Peoples R China
[2] Univ Calif Berkeley, Sch Publ Hlth, Dept Virol, Berkeley, CA 94720 USA
来源
PLOS ONE | 2013年 / 8卷 / 12期
基金
中国国家自然科学基金;
关键词
STEM-CELLS; DIFFERENTIATION; EXPRESSION; CLUSTER; APOPTOSIS; PATHWAY; TRANSDUCTION; RECEPTORS; MICRORNAS; MECHANISM;
D O I
10.1371/journal.pone.0083067
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
Bone morphogenetic protein (BMP) signaling is active in many tissues including the central nervous system, in which it regulates cell proliferation, differentiation and maturation. The modulation of BMP pathway is crucial since abnormality of BMP signaling may cause cellular malfunction such as apoptosis. There are evidences indicating that miR-17 family is involved in the BMP signaling. In the present study, we demonstrated that BMP2 stimulation directly increased the transcription of miR-17-92 and miR-106b-25 cluster via Smad activation, which leads to the up-regulation of mature miR-17/20a/93. In addition, we provided evidence that BMP2 activation repressed BMPRII expression through modulating miR-17 family in primary neurons. Furthermore, we proved that such negative regulation protected neurons from apoptosis induced by abnormal BMP signaling. Taken together, these results suggest a regulatory pathway of BMP-miR-17 family-BMPRII, which consist a negative feedback loop that balances BMP signaling and maintains cell homeostasis in neurons.
引用
收藏
页数:11
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