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依赖Dicer的途径通过调控Runx2对成骨作用有贡献。

Dicer-dependent pathway contribute to the osteogenesis mediated by regulation of Runx2.

作者信息

Zhou Jie, Hu Yun, Chen Yang, Yang Lan, Song Jinlin, Tang Yuying, Deng Feng, Zheng Leilei

机构信息

College of Stomatology, Chongqing Medical UniversityChongqing 401147, P. R. China; Chongqing Key Laboratory of Oral Diseases and Biomedical SciencesChongqing 401147, P. R. China; Chongqing Municipal Key Laboratory of Oral Biomedical Engineering of Higher EducationChongqing 401147, P. R. China.

College of Stomatology, Chongqing Medical University Chongqing 401147, P. R. China.

出版信息

Am J Transl Res. 2016 Dec 15;8(12):5354-5369. eCollection 2016.

Abstract

Osteogenesis is mediated by sophisticated interactions of various molecular functions and biological processes, including post-transcriptional regulation. A range of miRNAs have been reported to regulate bone homeostasis and osteoblasts differentiation either positively or negatively through multiple signaling pathways. RNase III endonuclease Dicer is the key enzyme required for the biogenesis of miRNAs and small interfering RNAs. To determine the global influence of miRNAs on regulation of osteogenesis of pre-osteoblast cells, the transcriptional regulation of Dicer and the function of Dicer during osteoblast differentiation and mineralization were investigated. Runx2 binding directly to the Dicer promoter region was characterized in MC3T3-E1 cells by chromatin immunoprecipitation (ChIP) and luciferase promoter reporter assays. Overexpression or knockdown of Runx2 resulted in increase or decrease of Dicer expression, respectively. Furthermore, abatement of Dicer in MC3T3-E1 cells down-regulated the expression of osteogenic marker genes and mineralization ability, at least partly involving Dicer-dependent processing of the miR-21a-5p targeting PTEN via pAKT/pGSK3β/β-catenin signaling pathways. Taken together, the study demonstrates the role of Dicer in osteogenesis and suggests that Dicer is required, in part, for Runx2 regulation of osteoblast differentiation.

摘要

骨生成由多种分子功能和生物学过程的复杂相互作用介导,包括转录后调控。据报道,一系列微小RNA(miRNA)通过多种信号通路正向或负向调节骨稳态和成骨细胞分化。核糖核酸酶III内切核酸酶Dicer是miRNA和小干扰RNA生物合成所需的关键酶。为了确定miRNA对前成骨细胞骨生成调节的整体影响,研究了Dicer在成骨细胞分化和矿化过程中的转录调控及功能。通过染色质免疫沉淀(ChIP)和荧光素酶启动子报告基因检测,在MC3T3-E1细胞中鉴定出Runx2直接与Dicer启动子区域结合。Runx2的过表达或敲低分别导致Dicer表达的增加或减少。此外,MC3T3-E1细胞中Dicer的减少下调了成骨标记基因的表达和矿化能力,至少部分涉及Dicer依赖的通过pAKT/pGSK3β/β-连环蛋白信号通路靶向PTEN的miR-21a-5p的加工。综上所述,该研究证明了Dicer在骨生成中的作用,并表明Dicer部分是Runx2调节成骨细胞分化所必需的。

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