首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >The effect of SIRT6 on the odontoblastic potential of Human Dental Pulp Cells
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The effect of SIRT6 on the odontoblastic potential of Human Dental Pulp Cells

机译:SIRT6对人牙髓细胞牙釉质形成的影响

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Introduction The aim of this study was to investigate whether SIRT6 is expressed in human dental pulp as well as the effect of SIRT6 on proliferation and odontoblastic differentiation of human dental pulp cells (HDPCs). Methods Immunohistochemical and immunocytochemical assays were used to detect the expression of SIRT6 in human dental pulp tissue and HDPCs. To determine the effect of SIRT6 on odontoblast differentiation, HDPCs with loss (HDPCs SIRT6 knockdown) and gain (HDPCs SIRT6 overexpression) of SIRT6 function were developed, and their proliferation ability was examined. Odontogenic differentiation of HDPCs was determined by alkaline phosphatase (ALP) activity, ALP-positive cell staining, alizarin red staining, and von Kossa staining. Mineralization-related genes, including ALP, dentin sialophosphoprotein (DSPP), and dentin matrix acidic phosphoprotein 1, were determined by real-time quantitative polymerase chain reaction. Western blot analysis was performed to detect the expression of DSPP protein. Results SIRT6 was found in the dental pulp tissue and HDPCs. SIRT6 knockdown decreased ALP activity in HDPCs; calcium nodule formation ability; and the expression of mineralization-related genes such as ALP, DSPP, and DMP1, whereas these were increased with the overexpression of SIRT6. Conclusions SIRT6 is expressed in human dental pulp and participates in the odontoblast differentiation of HDPCs.
机译:引言这项研究的目的是研究SIRT6是否在人牙髓中表达以及SIRT6对人牙髓细胞(HDPC)增殖和成牙本质分化的影响。方法采用免疫组织化学和免疫细胞化学方法检测SIRT6在牙髓组织和HDPCs中的表达。为了确定SIRT6对成牙本质细胞分化的影响,开发了具有SIRT6功能丧失(HDPCs SIRT6敲低)和获得(HDPCs SIRT6过表达)的HDPC,并检查了它们的增殖能力。通过碱性磷酸酶(ALP)活性,ALP阳性细胞染色,茜素红染色和von Kossa染色来确定HDPC的成牙细胞分化。通过实时定量聚合酶链反应确定与矿化有关的基因,包括ALP,牙本质唾液磷蛋白(DSPP)和牙本质基质酸性磷蛋白1。进行蛋白质印迹分析以检测DSPP蛋白的表达。结果在牙髓组织和HDPCs中发现了SIRT6。 SIRT6敲低降低了HDPC中的ALP活性;钙结节形成能力;矿化相关基因(如ALP,DSPP和DMP1)的表达,而这些随SIRT6的过表达而增加。结论SIRT6在人牙髓中表达,并参与HDPC的成牙本质细胞分化。

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