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The Crosstalk between HDPSCs and HUCMSCs on Proliferation and Osteogenic Genes Expression in Coculture System

机译:HDPSC与HUCMSC在共培养系统中增殖和成骨基因表达的串扰

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摘要

>Objectives: The present study established a non-contact coculture system in vitro, aiming to investigate the crosstalk between human dental pulp stem cells (hDPSCs) and human umbilical cord mesenchymal stem cells (hUCMSCs) on proliferation activity and osteogenic genes expression through paracrine.>Materials and methods: The stemness of hDPSCs and hUCMSCs were identified by flow cytometric analysis and multipotential differentiation assays. With the help of transwell inserts, the non-contact coculture system in vitro was established between hDPSCs and hUCMSCs. EdU labeling analysis and Western Blot were used to detect the proliferation activity. The mRNA and protein levels of osteogenic genes were evaluated by RT-PCR and Western Blot. The expression of elements in Akt/mTOR signaling pathway were detected by Western Blot.>Results: Both hDPSCs and hUCMSCs were positive to MSCs specific surface markers and had multi-differentiation potential. The proportion of EdU-positive cells increased and the expression of CDK6 and CYCLIN A were up-regulated in cocultured hDPSCs. Both prior coculture and persistent coculture improved mRNA and protein levels of osteogenic genes in hDPSCs. While in cocultured hUCMSCs, no statistical differences were observed on proliferation and osteogenesis. The phosphorylation of Akt and mTOR was up-regulated in cocultured hDPSCs.>Conclusions: The crosstalk between hDPSCs and hUCMSCs in coculture system increased the proliferation activity and enhanced osteogenic genes expression in hDPSCs. Akt/mTOR signaling pathway might take part in the enhancing effects in both cell proliferation and gene expression.
机译:>目的:本研究建立了体外非接触式共培养系统,旨在研究人牙髓干细胞(hDPSCs)与人脐带间充质干细胞(hUCMSCs)之间的串扰以及增殖活性。 >材料和方法:通过流式细胞术和多能分化分析法鉴定了hDPSCs和hUCMSCs的干性。借助transwell插入片段,在hDPSC和hUCMSC之间建立了体外非接触式共培养系统。 EdU标记分析和Western Blot用于检测增殖活性。通过RT-PCR和Western Blot评估成骨基因的mRNA和蛋白质水平。 Western Blot检测Akt / mTOR信号通路中各元素的表达。>结果:hDPSCs和hUCMSCs均对MSCs的特异性表面标志物呈阳性,并具有多分化潜能。共培养的hDPSCs中EdU阳性细胞比例增加,CDK6和CYCLIN A的表达上调。既往共培养和持续共培养均改善了hDPSCs中成骨基因的mRNA和蛋白质水平。在共培养的hUCMSCs中,在增殖和成骨方面未观察到统计学差异。共培养hDPSCs中Akt和mTOR的磷酸化上调。>结论:共培养系统中hDPSCs与hUCMSCs之间的串扰增加了hDPSCs的增殖活性并增强了成骨基因的表达。 Akt / mTOR信号通路可能参与细胞增殖和基因表达的增强作用。

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