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Effects of the enamel matrix derivative on the proliferation and odontogenic differentiation of human dental pulp cells

机译:釉质基质衍生物对人牙髓细胞增殖和牙源性分化的影响

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Objective The enamel matrix derivative (EMD) has a positive effect on the proliferation of human periodontal ligament cells and the healing of periodontal tissues. The aim of this study was to evaluate the effects of EMD on the proliferation and differentiation of human dental pulp cells (hDPCs) in vitro. Methods hDPCs were isolated from human impacted third molars and cultured in vitro. After treatment with100 μg/mL EMD, the proliferation of hDPCs was determined by a cell counting kit 8 (CCK8) assay. After incubation in EMD osteogenic induction medium for 14 days, the osteogenic differentiation of hDPCs was evaluated by alkaline phosphatase (ALP) activity, alizarin staining and the expression of osteogenesis-related genes. Results The EMD osteogenic induction medium enhanced the proliferation of hDPCs. After osteogenic induction, EMD increased the osteogenic potential of hDPCs, as measured by alkaline phosphatase activity and calcium accumulation; the expression levels of osteogenesis-related genes, such as ALP, DSPP, BMP, and OPN were also upregulated. In addition, the expression levels of odontogenesis-related transcription factors Osterix and Runx2 were upregulated. Conclusions EMD could enhance the mineralization of hDPSCs upregulated the expression of markers for odontoblast/osteoblast-like cells. Further studies are required to determine if EMD can improve pulp tissue repair and regeneration.
机译:目的釉质基质衍生物(EMD)对人牙周膜细胞的增殖和牙周组织的修复具有积极作用。这项研究的目的是评估EMD在体外对人牙髓细胞(hDPC)增殖和分化的影响。方法从人感染的第三磨牙中分离出hDPC并进行体外培养。用100μg/ mL EMD处理后,通过细胞计数试剂盒8(CCK8)测定来确定hDPC的增殖。在EMD成骨诱导培养基中孵育14天后,通过碱性磷酸酶(ALP)活性,茜素染色和成骨相关基因的表达来评估hDPC的成骨分化。结果EMD成骨诱导培养基能促进hDPCs的增殖。成骨诱导后,EMD通过碱性磷酸酶活性和钙积累来测量增加了hDPC的成骨潜能。骨形成相关基因如ALP,DSPP,BMP和OPN的表达水平也被上调。此外,与成牙相关的转录因子Osterix和Runx2的表达水平也被上调。结论EMD可增强hDPSCs的矿化作用,上调成牙本质细胞/成骨细胞样细胞标志物的表达。需要进一步研究以确定EMD是否可以改善牙髓组织的修复和再生。

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