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Sox9 调控的 miRNA-574-3p 抑制间充质干细胞的软骨分化。

Sox9-regulated miRNA-574-3p inhibits chondrogenic differentiation of mesenchymal stem cells.

机构信息

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

出版信息

PLoS One. 2013 Apr 23;8(4):e62582. doi: 10.1371/journal.pone.0062582. Print 2013.

Abstract

The aim of this study was to identify new microRNAs (miRNAs) that are modulated during the differentiation of mesenchymal stem cells (MSCs) toward chondrocytes. Using large scale miRNA arrays, we compared the expression of miRNAs in MSCs (day 0) and at early time points (day 0.5 and 3) after chondrogenesis induction. Transfection of premiRNA or antagomiRNA was performed on MSCs before chondrogenesis induction and expression of miRNAs and chondrocyte markers was evaluated at different time points during differentiation by RT-qPCR. Among miRNAs that were modulated during chondrogenesis, we identified miR-574-3p as an early up-regulated miRNA. We found that miR-574-3p up-regulation is mediated via direct binding of Sox9 to its promoter region and demonstrated by reporter assay that retinoid X receptor (RXR)α is one gene specifically targeted by the miRNA. In vitro transfection of MSCs with premiR-574-3p resulted in the inhibition of chondrogenesis demonstrating its role during the commitment of MSCs towards chondrocytes. In vivo, however, both up- and down-regulation of miR-574-3p expression inhibited differentiation toward cartilage and bone in a model of heterotopic ossification. In conclusion, we demonstrated that Sox9-dependent up-regulation of miR-574-3p results in RXRα down-regulation. Manipulating miR-574-3p levels both in vitro and in vivo inhibited chondrogenesis suggesting that miR-574-3p might be required for chondrocyte lineage maintenance but also that of MSC multipotency.

摘要

本研究旨在鉴定在间充质干细胞(MSCs)向软骨细胞分化过程中被调控的新 microRNA(miRNA)。我们使用大规模 miRNA 芯片,比较了 MSC(第 0 天)和软骨生成诱导后早期(第 0.5 天和第 3 天)miRNA 的表达。在软骨生成诱导前对 MSC 进行 premiRNA 或 antagomiRNA 转染,并通过 RT-qPCR 在分化过程中的不同时间点评估 miRNA 和软骨细胞标志物的表达。在软骨生成过程中被调控的 miRNA 中,我们鉴定出 miR-574-3p 是一种早期上调的 miRNA。我们发现 miR-574-3p 的上调是通过 Sox9 与其启动子区域的直接结合介导的,并通过报告基因实验证明视黄酸受体(RXR)α是 miRNA 特异靶向的一个基因。MSCs 中 premiR-574-3p 的体外转染导致软骨生成抑制,证明其在 MSC 向软骨细胞分化过程中的作用。然而,在异位骨化模型中,miR-574-3p 的表达上调和下调都抑制了向软骨和骨的分化。总之,我们证明 Sox9 依赖性 miR-574-3p 的上调导致 RXRα 的下调。miR-574-3p 水平的体外和体内操纵均抑制软骨生成,表明 miR-574-3p 可能是软骨细胞谱系维持所必需的,但也是 MSC 多能性所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3018/3633883/5d7b421fa599/pone.0062582.g001.jpg

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