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人脂肪来源干细胞成软骨分化过程中 microRNAs 的表达。

Expression of microRNAs during chondrogenesis of human adipose-derived stem cells.

机构信息

Department of Joint Surgery, First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

Osteoarthritis Cartilage. 2012 Dec;20(12):1638-46. doi: 10.1016/j.joca.2012.08.024. Epub 2012 Sep 1.

Abstract

OBJECTIVES

MicroRNAs (miRNAs) play an important role in the regulation of chondrogenesis of mesenchymal stem cells, but their expression still remains unknown in human adipose-derived stem cells (hADSCs). In this study the miRNA expression profile during chondrogenic differentiation of hADSC and the potential mechanism whereby miRNAs may affect the process of chondrogenesis are considered.

METHODS

hADSCs were isolated and cultured. The expression of chondrogenic proteins was detected using enzyme-linked immunosorbent assay (ELISA). miRNA expression profiles before and after chondrogenic induction were obtained using miRNA microarray essay and differently expressed miRNAs were primarily verified using quantitative real-time polymerase chain reaction (qRT-PCR). Putative targets of the miRNAs were predicted using online software programs MiRanda, TargetScan and miRBase.

RESULTS

Twelve miRNAs were found to be differentially expressed pre- and post-chondrogenic induction by over a two-fold change, including eight up-regulated miRNAs (miR-193b, miR-199a-3p/hsa-miR-199b-3p, miR-455-3p, miR-210, miR-381, miR-92a, miR-320c, and miR-136), and four down-regulated miRNAs (miR-490-5p, miR-4287, miR-BART8*, and miR-US25-1*). qRT-PCR analysis further confirmed these results. Predicted target genes of the differentially expressed miRNAs were based on the overlap of at least two online prediction algorithms, with the known functions of regulating chondrogenic differentiation, self-renewal, signal transduction and cell cycle control.

CONCLUSIONS

In this study we have identified a group of miRNAs and their target genes, which may play important roles in regulating chondrogenic differentiation of hADSCs. Our results provide the basis for further investigation into the molecular mechanism of chondrogenesis in hADSCs and their differentiation for cartilage engineering.

摘要

目的

微小 RNA(miRNAs)在间充质干细胞的软骨生成中发挥重要作用,但它们在人脂肪来源干细胞(hADSCs)中的表达仍不清楚。本研究探讨了 hADSC 软骨生成分化过程中的 miRNA 表达谱,以及 miRNAs 影响软骨生成过程的潜在机制。

方法

分离和培养 hADSCs。采用酶联免疫吸附试验(ELISA)检测软骨生成蛋白的表达。使用 miRNA 微阵列检测 hADSC 软骨诱导前后的 miRNA 表达谱,并用定量实时聚合酶链反应(qRT-PCR)初步验证差异表达的 miRNA。使用在线软件程序 MiRanda、TargetScan 和 miRBase 预测 miRNA 的假定靶标。

结果

通过 miRNA 微阵列检测到软骨诱导前后有 12 个 miRNA 的表达发生了两倍以上的差异变化,其中 8 个上调 miRNA(miR-193b、miR-199a-3p/hsa-miR-199b-3p、miR-455-3p、miR-210、miR-381、miR-92a、miR-320c 和 miR-136)和 4 个下调 miRNA(miR-490-5p、miR-4287、miR-BART8和 miR-US25-1)。qRT-PCR 分析进一步证实了这些结果。差异表达 miRNA 的预测靶基因基于至少两种在线预测算法的重叠,这些靶基因具有调节软骨生成分化、自我更新、信号转导和细胞周期控制的已知功能。

结论

本研究鉴定了一组 miRNA 及其靶基因,它们可能在调节 hADSC 的软骨生成分化中发挥重要作用。我们的研究结果为进一步研究 hADSC 软骨生成的分子机制及其在软骨工程中的分化提供了基础。

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