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Effects of simulated microgravity on the expression profiles of RNA during osteogenic differentiation of human bone marrow mesenchymal stem cells

机译:模拟微匍匐在人骨髓间充质干细胞骨质骨髓间质分化期间RNA表达谱的影响

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摘要

Objectives Exposure to microgravity induces many adaptive and pathological changes in human bone marrow mesenchymal stem cells (hBMSCs). However, the underlying mechanisms of these changes are poorly understood. We revealed the gene expression patterns of hBMSCs under normal ground (NG) and simulated microgravity (SMG), which showed an interpretation for these changes by gene regulation and signal pathways analysis. Materials and methods In this study, hBMSCs were osteogenically induced for 0, 2, 7 and 14 days under normal ground gravity and simulated microgravity, followed by analysis of the differences in transcriptome expression during osteogenic differentiation by RNA sequencing and some experimental verification for these results. Results The results indicated that 837, 399 and 894 differentially expressed genes (DEGs) were identified in 2, 7 and 14 days samples, respectively, out of which 13 genes were selected for qRT-PCR analysis to confirm the RNA-sequencing results. After analysis, we found that proliferation was inhibited in the early stage of induction. In the middle stage, osteogenic differentiation was inhibited, whereas adipogenic differentiation benefited from SMG. Moreover, SMG resulted in the up-regulation of genes specific for tumorigenesis in the later stage. Conclusion Our data revealed that SMG inhibits the proliferation and inhibits the differentiation towards osteoblasts but promotes adipogenesis. SMG also selects highly tumorigenic cells for survival under prolonged SMG.
机译:目的暴露于微再生诱导人骨髓间充质干细胞(HBMSCs)中的许多适应性和病理变化。然而,这些变化的潜在机制被理解得很差。我们揭示了正常研磨(Ng)和模拟微匍匐(SMG)下HBMSCs的基因表达模式,其显示了通过基因调控和信号途径分析对这些变化的解释。本研究中的材料和方法,HBMSCs在正常地重力和模拟微匍匐的情况下致致溶解0,2,7和14天,然后分析通过RNA测序的成骨分化期间转录组表达的差异以及这些结果的一些实验验证。结果结果表明,在2,7和14天的样品中鉴定出837,399和894个差异表达基因(DEGS),其中选择了13个基因用于QRT-PCR分析以确认RNA测序结果。经过分析后,我们发现在诱导的早期阶段抑制了增殖。在中间阶段,抑制了成骨分化,而脂肪生成分化受益于SMG。此外,SMG导致在后期肿瘤发生的基因的上调。结论我们的数据显示,SMG抑制增殖并抑制对成骨细胞的分化,但促进脂肪发生。 SMG还在延长SMG下选择高度致瘤细胞的存活。

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