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Amniotic fluid-derived mesenchymal stem cells lead to bone differentiation when cocultured with dental pulp stem cells

机译:与牙髓干细胞共培养时,羊水来源的间充质干细胞导致骨分化

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摘要

Mesenchymal stem cells are present in many tissues of the human body, including amniotic fluid (AF) and dental pulp (DP). Stem cells of both AF and DP give rise to a variety of differentiated cells. In our experience, DP stem cells (DPSCs) display a high capacity to produce bone. Therefore, our aim was to investigate if AF-derived stem cells (AFSCs) were able to undergo bone differentiation in the presence of DPSCs. AFSCs were seeded under three different conditions: (i) cocultured with DPSCs previously differentiated into osteoblasts; (ii) cultured in the conditioned medium of osteoblast-differentiated DPSCs; (iii) cultured in the osteogenic medium supplemented with vascular endothelial growth factor and bone morphogenetic protein-2 (BMP-2). Results showed that AFSCs were positive for mesenchymal markers, and expressed high levels of Tra1-60, Tra1-80, BMPR1, BMPR2, and BMP-2. In contrast, AFSCs were negative for epithelial and hematopoietic/endothelial markers. When AFSCs were cocultured with DPSCs-derived osteoblasts, they differentiated into osteoblasts. A similar effect was observed when AFSCs were cultured in the presence of a conditioned medium originated from DPSCs. We found that osteoblasts derived from DPSCs released large amounts of BMP-2 and vascular endothelial growth factor into the culture medium and that those morphogens significantly upregulate RUNX-2 gene, stimulating osteogenesis. This study highlights the mechanisms of osteogenesis and strongly suggests that the combination of AFSCs with DPSCs may provide a rich source of soluble proteins useful for bone engineering purposes.
机译:间充质干细胞存在于人体的许多组织中,包括羊水(AF)和牙髓(DP)。 AF和DP的干细胞均可产生多种分化细胞。根据我们的经验,DP干细胞(DPSC)显示出高能力生产骨骼。因此,我们的目的是研究在DPSC存在下,AF衍生干细胞(AFSC)是否能够经历骨分化。 AFSCs在三种不同条件下接种:(i)与先前分化为成骨细胞的DPSCs共培养; (ii)在成骨细胞分化的DPSC的条件培养基中培养; (iii)在补充有血管内皮生长因子和骨形态发生蛋白2(BMP-2)的成骨培养基中培养。结果表明,AFSCs为间充质标记阳性,并表达高水平的Tra1-60,Tra1-80,BMPR1,BMPR2和BMP-2。相反,AFSCs的上皮和造血/内皮标志物阴性。当AFSC与DPSC衍生的成骨细胞共培养时,它们分化为成骨细胞。当在源自DPSC的条件培养基的存在下培养AFSC时,观察到类似的效果。我们发现衍生自DPSC的成骨细胞向培养基中释放了大量BMP-2和血管内皮生长因子,而这些形态原显着上调RUNX-2基因,从而刺激成骨作用。这项研究突出了成骨的机制,并强烈建议将AFSC与DPSC结合使用可提供丰富的可溶性蛋白质来源,可用于骨骼工程。

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