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Demineralized Dentin Matrix Induces Odontoblastic Differentiation of Dental Pulp Stem Cells

机译:脱矿的牙本质基质诱导牙髓干细胞的成牙本质细胞分化。

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The aim of this study was to investigate the effect of demineralized dentin matrix (DDM) on dental pulp stem cells (DPSCs) and the potential of complexes with DPSCs and DDM for mineralized tissue formation. Stem cells derived from the dental pulp of healthy pigs aged 18 months were isolated and cultured. DPSCs were incubated with alpha minimum essential medium treated with DDM extract at 1 mg/ml (DDM1) or 10 mg/ml (DDM10). The concentrations of 3 growth factors in DDM extract was measured by enzyme-linked immunosorbent assay. Adhesion of DPSCs on DDM and hydroxyapatite-tricalcium phosphate (HA-TCP) surfaces was observed using scanning electron microscopy. Cell proliferation was evaluated with cell counting kit-8 and migration by Transwell migration assays. Odontoblastic differentiation was assessed by alkaline phosphatase (ALP) and alizarin red staining, ALP activity and real-time polymerase chain reaction analysis of markers of ALP, runt-related transcription factor 2, type I collagen, dentin matrix acidic phosphoprotein-1, osteonectin and dentin sialophosphoprotein (DSPP). Finally, DPSCs were combined with DDM and placed subcutaneously in nude mice for 12 weeks; DPSCs combined with HA-TCP and DDM alone served as controls. DDM could promote DPSC adhesion, migration and odontoblastic differentiation. Mineralized tissue formation was observed with the DPSC and DDM combination and the DPSC and HATCP combination. The mineralized tissue of the DPSC + DDM combination stained positive for DSPP, similar to the dentin tissue. These results indicate that DDM induces DPSC odontoblastic differentiation, suggesting applications for dentin regeneration. (C) 2015 S. Karger AG, Basel
机译:这项研究的目的是研究脱矿的牙本质基质(DDM)对牙髓干细胞(DPSC)的影响以及与DPSC和DDM形成复合物形成矿化组织的潜力。分离并培养源自18个月大健康猪的牙髓的干细胞。将DPSC与以1 mg / ml(DDM1)或10 mg / ml(DDM10)的DDM提取物处理过的α最低限度必需培养基孵育。通过酶联免疫吸附法测定DDM提取物中3种生长因子的浓度。使用扫描电子显微镜观察到DPSC在DDM和羟基磷灰石-磷酸三钙(HA-TCP)表面上的粘附。用细胞计数试剂盒8评估细胞增殖,并通过Transwell迁移测定法评估迁移。通过碱性磷酸酶(ALP)和茜素红染色,ALP活性和ALP标记,矮子相关转录因子2,I型胶原,牙本质基质酸性磷酸蛋白1,骨粘连蛋白和牙本质唾液磷蛋白(DSPP)。最后,将DPSC与DDM组合并在裸鼠中皮下放置12周。结合HA-TCP和DDM的DPSC单独用作对照。 DDM可以促进DPSC粘附,迁移和成牙本质分化。用DPSC和DDM组合以及DPSC和HATCP组合观察到矿化的组织形成。与牙本质组织相似,DPSC + DDM组合的矿化组织对DSPP染色呈阳性。这些结果表明,DDM诱导DPSC牙本质细胞分化,表明其在牙本质再生中的应用。 (C)2015 S.Karger AG,巴塞尔

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