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首页> 外文期刊>BMC Oral Health >Different concentrations of C5a affect human dental pulp mesenchymal stem cells differentiation
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Different concentrations of C5a affect human dental pulp mesenchymal stem cells differentiation

机译:不同浓度的C5a影响人牙髓间充质干细胞分化

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During the process of deep decay, when decay approaches the pulp, an immune response is triggered inside the pulp, which activates the complement cascade. The effect of complement component 5a (C5a) on the differentiation of dental pulp mesenchymal stem cells (DPSCs) is related to dentin reparation. The aim of the present study was to stimulate DPSCs with different concentrations of C5a and evaluate the differentiation of odontoblasts using dentin sialoprotein (DSP). DPSCs were divided into the following six groups: (i) Control; (ii) DPSCs treated with 50?ng/ml C5a; (iii) DPSCs treated with 100?ng/ml C5a; (iv) DPSCs treated with 200?ng/ml C5a; (v) DPSCs treated with 300?ng/ml C5a; and (vi) DPSCs treated with 400?ng/ml C5a. Flow cytometry and multilineage differentiation potential were used to identify DPSCs. Mineralization induction, Real-time PCR and Western blot were conducted to evaluate the differentiation of odontoblast in the 6 groups. DPSCs can express mesenchymal stem cell markers, including CD105, CD90, CD73 and, a less common marker, mesenchymal stromal cell antigen-1. In addition, DPSCs can differentiate into adipocytes, neurocytes, chondrocytes and odontoblasts. All six groups formed mineralized nodules after 28?days of culture. Reverse transcription-quantitative PCR and western blotting indicated that the high concentration C5a groups expressed higher DSP levels and promoted DPSC differentiation, whereas the low concentration C5a groups displayed an inhibitory effect. In this study, the increasing concentration of C5a, which accompanies the immune process in the dental pulp, has demonstrated an enhancing effect on odontoblast differentiation at higher C5a concentrations in vitro.
机译:在深衰减过程中,当衰减接近纸浆时,在纸浆内触发免疫应答,该纸浆激活补体级联。补体组分5a(c5a)对牙髓间充质干细胞(DPSCs)分化的影响与牙本质替换有关。本研究的目的是刺激具有不同浓度C5A的DPSC,并评估使用牙本质唾液蛋白(DSP)的牙卵细胞的分化。 DPSCS分为以下六组:(i)控制; (ii)用50μg/ ml C5a处理的DPSC; (iii)用100μg/ ml C5a处理的DPSC; (iv)用200μg/ ml c5a处理的DPSC; (v)用300μg/ ml C5a处理的DPSC; (VI)用400μg/ ml C5a处理的DPSC。流式细胞术和多线粒分化潜力用于鉴定DPSC。进行矿化诱导,进行实时PCR和Western印迹,以评估6组中Odontoblast的分化。 DPSC可以表达间充质干细胞标记物,包括CD105,CD90,CD73和较少的常见标记,间充质基质细胞抗原-1。此外,DPSC可以分化为脂肪细胞,神经细胞,软骨细胞和Odontoblasts。所有六组在28例培养后形成矿化结节。逆转录定量PCR和Western印迹表明,高浓度C5a基团表达较高的DSP水平并促进DPSC分化,而低浓度C5a基团显示出抑制作用。在该研究中,伴随着牙科纸浆中免疫过程的C5a浓度的增加表明,在体外较高C5A浓度下的卵黄细胞分化的增加。

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