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首页> 外文期刊>Connective tissue research >1,25-Dihydroxyvitamin D-3 stimulates odontoblastic differentiation of human dental pulp-stem cells in vitro
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1,25-Dihydroxyvitamin D-3 stimulates odontoblastic differentiation of human dental pulp-stem cells in vitro

机译:1,25-二羟基维生素D-3在体外刺激人牙牙髓干细胞的Odontobolas弹性分化

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摘要

Background: 1,25-Dihydroxyvitamin D-3 (1,25-OH D-3) plays an important role in mineralized tissue metabolism, including teeth. However, few studies have addressed its role in odontoblastic differentiation of human dental pulp-stem cells (hDPSCs). Aim: This study aimed to understand the influence of various concentrations of 1,25-OH D-3 on the proliferation capacity and early dentinogenesis responses of hDPSCs. Materials and Methods: hDPSCs were obtained from the impacted third molar teeth. Monolayer cultured cells were incubated with a differentiation medium containing different concentrations of 1,25-OH D-3 (0.001, 0.01, and 0.1 mu M). All groups were evaluated by S-phase rate [immunohistochemical (IHC) bromodeoxyuridine (BrdU) staining], STRO-1 and dentin sialoprotein (DSP)+ levels (IHC), and alkaline phosphatase (ALP, enzyme-linked immunosorbent assay (ELISA)) levels. Results: The number of cells that entered the S-phase was determined to be the highest and lowest in the control and 0.001 mu M 1,25-OH D-3 groups, respectively. The 0.1 mu M vitamin D-3 group had the highest increase in DSP+ levels. The highest Stro-1 levels were detected in the control and 0.1 mu M 1,25-OH D-3 groups, respectively. The 0.1 mu M 1,25-OH D-3 induced a mild increase in ALP activity. Conclusions: This study demonstrated that 1,25-OH D-3 stimulated odontoblastic differentiation of hDPSCs in vitro in a dose-dependent manner. The high DSP + cell number and a mild increase in ALP activity suggest that DPSCs treated with 0.1 M 1,25-OH D-3 are in the later stage of odontoblastic differentiation. The results confirm that 1,25-OH D-3-added cocktail medium provides a sufficient microenvironment for the odontoblastic differentiation of hDPSCs in vitro.
机译:背景:1,25-二羟基维胺D-3(1,25-OH D-3)在矿化组织代谢中起重要作用,包括牙齿。然而,很少有研究已经解决了其在人牙牙髓 - 干细胞(HDPSC)的异常分化中的作用。目的:本研究旨在了解各种浓度1,25-OH D-3对HDPSC的增殖能力和早期牙进发生反应的影响。材料和方法:从受冲击的第三磨牙中获得HDPSC。将单层培养的细胞与含有不同浓度为1,25-OH D-3(0.001,0.01和0.1μm)的分化培养基孵育。通过S相速率[免疫组织化学(IHC)溴氧脲素(BrdU)染色],Stro-1和牙本质蛋白(DSP)+水平(IHC)和碱性磷酸酶(ALP,酶联免疫吸附测定(ELISA)进行评估)水平。结果:将进入S相的细胞数决定为对照中最高,最低,最低,分别为0.001μm1,25-OH D-3组。 0.1 mu m的维生素D-3组的DSP +水平的增加最高。在对照和0.1μm1,25-OH D-3组中检测到最高的它们的级别水平。 0.1μm1,25-OH D-3诱导ALP活性的温和增加。结论:该研究表明,1,25-OH D-3以剂量依赖性方式在体外刺激HDPSCs的Odontobolas弹性分化。高DSP +细胞数和ALP活性的轻度增加表明,用0.1M1,25-OH D-3处理的DPSC在OdontoBolas弹性分化的后期。结果证实,1,25-OH D-3添加的鸡尾酒培养基提供了足够的微环境,用于体外HDPSC的Odontobolas弹性分化。

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