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miRNA-29a 调控 FOXO3A 对间充质干细胞软骨向分化及软骨形成的作用。

FOXO3A regulation by miRNA-29a Controls chondrogenic differentiation of mesenchymal stem cells and cartilage formation.

机构信息

1 Inserm, U 844, Hôpital Saint-Eloi , Montpellier, France .

出版信息

Stem Cells Dev. 2014 Jun 1;23(11):1195-205. doi: 10.1089/scd.2013.0463. Epub 2014 Mar 21.

DOI:10.1089/scd.2013.0463
PMID:24467486
Abstract

Skeletal development and cartilage formation require stringent regulation of gene expression for mesenchymal stem cells (MSCs) to progress through stages of differentiation. Since microRNAs (miRNAs) regulate biological processes, the objective of the present study was to identify novel miRNAs involved in the modulation of chondrogenesis. We performed miRNA profiling and identify miR-29a as being one of the most down-regulated miRNAs during the chondrogenesis. Using chromatin immunoprecipitation, we showed that SOX9 down-regulates its transcription. Moreover, the over-expression of miR-29a strongly inhibited the expression of chondrocyte-specific markers during in vitro chondrogenic differentiation of MSCs. We identified FOXO3A as a direct target of miR-29a and showed a down- and up-regulation of FOXO3a protein levels after transfection of, respectively, premiR- and antagomiR-29a oligonucleotides. Finally, we showed that using the siRNA or premiR approach, chondrogenic differentiation was inhibited to a similar extent. Together, we demonstrate that the down-regulation of miR-29a, concomitantly with FOXO3A up-regulation, is essential for the differentiation of MSCs into chondrocytes and in vivo cartilage/bone formation. The delivery of miRNAs that modulate MSC chondrogenesis may be applicable for cartilage regeneration and deserves further investigation.

摘要

骨骼发育和软骨形成需要严格调控间充质干细胞(MSCs)中的基因表达,以使它们能够经历分化阶段。由于 microRNAs(miRNAs)调控着生物过程,因此本研究的目的是鉴定参与软骨形成调控的新 miRNAs。我们进行了 miRNA 谱分析,发现 miR-29a 是软骨形成过程中下调最明显的 miRNAs 之一。通过染色质免疫沉淀实验,我们发现 SOX9 下调其转录。此外,在 MSC 的体外软骨分化过程中过表达 miR-29a 会强烈抑制软骨细胞特异性标志物的表达。我们鉴定出 FOXO3A 是 miR-29a 的直接靶标,并显示转染 premiR-和 antagomiR-29a 寡核苷酸后 FOXO3A 蛋白水平的下调和上调。最后,我们表明使用 siRNA 或 premiR 方法,软骨分化被抑制到相似的程度。综上所述,我们证明 miR-29a 的下调,伴随着 FOXO3A 的上调,对于 MSCs 向软骨细胞的分化以及体内软骨/骨形成是必不可少的。调节 MSC 软骨形成的 miRNAs 的递送可能适用于软骨再生,值得进一步研究。

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