Wang Liang, Wang Yipeng, Li Zhengyao, Li Ziquan, Yu Bin
Department of Orthopaedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 1 Shuaifuyuan Hutong, Beijing, 100730, China.
Int Orthop. 2015 May;39(5):1013-9. doi: 10.1007/s00264-015-2683-0. Epub 2015 Jan 30.
The purpose of this study was to investigate the differential expression and putative function of long noncoding RNAs (lncRNAs) during the osteogenic differentiation of human bone marrow mesenchymal stem cells (MSCs).
The differential lncRNAs expression profiles of undifferentiated and differentiated cells during osteogenic differentiation were established by lncRNA microarray. Microarray data were validated using quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Bioinformatic analyses (gene ontology, pathway and co-expression network analysis) were applied for further study of these differentially expressed lncRNAs.
A total of 1,206 differentially expressed lncRNAs were identified during the process of osteogenic differentiation. Among these lncRNAs, 687 were up-regulated and 519 were down-regulated more than two-fold. Bioinformatic analyses were applied for further study of these differentially expressed lncRNAs. Further analysis found 48 regulated enhancer-like lncRNA and 14 lincRNA. The dynamic expression trends H19 and uc022axw.1 were then observed using qRT-PCR. The results showed that the two up-regulated lncRNAs are likely to play important roles in osteogenic differentiation process.
Taken together, our study first revealed the expression profiles of lncRNAs in osteogenic differentiation of human bone marrow MSCs. It provides an experimental basis for further research on lncRNAs functions during osteogenic differentiation of human bone marrow MSCs.
本研究旨在调查长链非编码RNA(lncRNA)在人骨髓间充质干细胞(MSC)成骨分化过程中的差异表达及潜在功能。
通过lncRNA微阵列建立成骨分化过程中未分化及分化细胞的lncRNA差异表达谱。使用定量逆转录-聚合酶链反应(qRT-PCR)验证微阵列数据。应用生物信息学分析(基因本体论、通路及共表达网络分析)进一步研究这些差异表达的lncRNA。
在成骨分化过程中共鉴定出1206个差异表达的lncRNA。在这些lncRNA中,687个上调,519个下调超过两倍。应用生物信息学分析进一步研究这些差异表达的lncRNA。进一步分析发现48个调控的增强子样lncRNA和14个长链基因间非编码RNA。随后使用qRT-PCR观察H19和uc022axw.1的动态表达趋势。结果表明,这两个上调的lncRNA可能在成骨分化过程中发挥重要作用。
综上所述,我们的研究首次揭示了lncRNA在人骨髓间充质干细胞成骨分化中的表达谱。它为进一步研究lncRNA在人骨髓间充质干细胞成骨分化过程中的功能提供了实验依据。