Suppr超能文献

一个骨细胞分化的 microRNA 调控机制。

A microRNA regulatory mechanism of osteoblast differentiation.

机构信息

Department of Orthopedics, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan.

出版信息

Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20794-9. doi: 10.1073/pnas.0909311106. Epub 2009 Nov 20.

Abstract

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 muscle-specific 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.

摘要

越来越多的证据表明,微小 RNA(miRNAs)在脊椎动物和无脊椎动物中调节各种发育和内稳态事件。成骨细胞分化是骨骼正常发育和获得骨量的关键步骤;然而,非编码小 RNA(尤其是 miRNAs)在成骨细胞分化中的生理作用仍不清楚。在这里,我们通过对成骨细胞分化过程中 miRNAs 表达的综合分析,表明先前被视为肌肉特异性 miRNA 的 miR-206 是该过程的关键调节因子。miR-206 在成骨细胞中表达,并在成骨细胞分化过程中表达降低。在成骨细胞中过表达 miR-206 抑制其分化,反之,下调 miR-206 的表达则促进成骨细胞分化。计算机分析和分子实验表明,间隙连接蛋白 43(Cx43),成骨细胞中的主要间隙连接蛋白,是 miR-206 的靶标,在表达 miR-206 的成骨细胞中恢复 Cx43 的表达,可挽救 miR-206 对成骨细胞分化的抑制作用。最后,在成骨细胞中表达 miR-206 的转基因小鼠由于成骨细胞分化受损而表现出低骨量表型。我们的数据表明,miRNA 是成骨细胞分化的调节因子。

相似文献

1
A microRNA regulatory mechanism of osteoblast differentiation.一个骨细胞分化的 microRNA 调控机制。
Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20794-9. doi: 10.1073/pnas.0909311106. Epub 2009 Nov 20.
4
MiR-5100 promotes osteogenic differentiation by targeting Tob2.微小RNA-5100通过靶向Tob2促进成骨分化。
J Bone Miner Metab. 2017 Nov;35(6):608-615. doi: 10.1007/s00774-016-0799-y. Epub 2016 Nov 21.

引用本文的文献

4
Novel Biomarkers of Bone Metabolism.新型骨代谢生物标志物。
Nutrients. 2024 Feb 22;16(5):605. doi: 10.3390/nu16050605.

本文引用的文献

1
Genetic control of bone formation.基因控制骨形成。
Annu Rev Cell Dev Biol. 2009;25:629-48. doi: 10.1146/annurev.cellbio.042308.113308.
6
SMAD proteins control DROSHA-mediated microRNA maturation.SMAD蛋白控制DROSHA介导的微小RNA成熟。
Nature. 2008 Jul 3;454(7200):56-61. doi: 10.1038/nature07086. Epub 2008 Jun 11.
7
Gene regulation by transcription factors and microRNAs.转录因子和微小RNA对基因的调控。
Science. 2008 Mar 28;319(5871):1785-6. doi: 10.1126/science.1151651.
8
Small non-coding RNAs in animal development.动物发育中的小非编码RNA
Nat Rev Mol Cell Biol. 2008 Mar;9(3):219-30. doi: 10.1038/nrm2347.
10
Dicer-dependent pathways regulate chondrocyte proliferation and differentiation.依赖Dicer的信号通路调控软骨细胞的增殖与分化。
Proc Natl Acad Sci U S A. 2008 Feb 12;105(6):1949-54. doi: 10.1073/pnas.0707900105. Epub 2008 Jan 31.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验