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Analyses of key mRNAs and lncRNAs for different osteo‐differentiation potentials of periodontal ligament stem cell and gingival mesenchymal stem cell

机译:牙周韧带干细胞不同骨质分化电位和牙龈间充质干细胞的键MRNA和LNCRNA分析

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摘要

Both human periodontal ligament stem cells (hPDLSCs) and human gingival mesenchymal stem cells (hGMSCs) are candidate seed cells for bone tissue engineering, but the osteo‐differentiation ability of the latter is weaker than the former, and the mechanisms are unknown. To explore the potential regulation of mRNAs and long non‐coding RNAs (lncRNAs), this study obtained the gene expression profiles of hPDLSCs and hGMSCs in both undifferentiated and osteo‐differentiated conditions by microarray assay and then analysed the common and specific differentially expressed mRNAs and lncRNAs in hPDLSCs and hGMSCs through bioinformatics method. The results showed that 275 mRNAs and 126 lncRNAs displayed similar changing patterns in hPDLSCs and hGMSCs after osteogenic induction, which may regulate the osteo‐differentiation in both types of cells. In addition, the expression of 223 mRNAs and 238 lncRNAs altered only in hPDLSCs after osteogenic induction, and 177 mRNAs and 170 lncRNAs changed only in hGMSCs. These cell‐specific differentially expressed mRNAs and lncRNAs could underlie the different osteo‐differentiation potentials of hPDLSCs and hGMSCs. Finally, dickkopf Wnt signalling pathway inhibitor 1 (DKK1) was proved to be one regulator for the weaker osteo‐differentiation ability of hGMSCs through validation experiments. We hope these results help to reveal new mRNAs‐lncRNAs‐based molecular mechanism for osteo‐differentiation of hPDLSCs and hGMSCs and provide clues on strategies for improving stem cell–mediated bone regeneration.
机译:人牙周韧带干细胞(HPDLSC)和人牙龈间充质干细胞(HGMSCs)是骨组织工程的候选种子细胞,但后者的骨差异化能力比前者较弱,并且机制未知。为了探讨MRNA和长期非编码RNA(LNCRNA)的潜在调节,该研究通过微阵列测定获得了在未分化的和骨质分化的条件下HPDLSC和HGMSC的基因表达谱,然后分析了常见和特异的差异表达的MRNA和通过生物信息学方法在HPDLSCS和HGMSC中的LNCRNA。结果表明,在骨质发生诱导后,275mRNA和126 LNCRNA在HPDLSCs和HGMSC中显示出类似的变化模式,其可以调节两种类型的细胞中的骨分化。此外,在骨质发生诱导后仅在HPDLSC中的223 mRNA和238克朗的表达,而177mRNA和170LNCRNA仅在HGMSC中变化。这些细胞特异性差异表达的MRNA和LNCRNA可以利于HPDLSCs和HGMSCs的不同骨型分化电位。最后,证明DickKopf Wnt信号传导途径抑制剂1(DKK1)是HGMSCs通过验证实验的较弱骨分化能力的调节剂。我们希望这些结果有助于揭示基于MRNA-LNCRNA的基于MRNA-LNCRNA的分子机制,用于HPDLSCS和HGMSC的骨质分化,并提供关于改善干细胞介导的骨再生的策略的线索。

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