首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Effect of F68, F127, and P85 pluronic block copolymers on odontogenic differentiation of human tooth germ stem cells
【24h】

Effect of F68, F127, and P85 pluronic block copolymers on odontogenic differentiation of human tooth germ stem cells

机译:F68,F127和P85普朗尼克嵌段共聚物对人牙胚干细胞牙源性分化的影响

获取原文
获取原文并翻译 | 示例
       

摘要

Introduction The major challenge in dental pulp engineering is to make a successful combination of stem cells and biomaterials with the aim of providing the differentiation of stem cells into odontogenic cell types. Among biomaterials, some types of pluronics have been reported to increase bone formation of stem cells. The effect of these pluronics on odontogenic differentiation has not been addressed yet. This study aimed to examine the effect of pluronics F68, F127, and P85 on odontogenic differentiation of stem cells derived from third molar tooth germs of young adults. Methods Human tooth germ stem cells (hTGSCs) were induced to differentiate into odontogenic cells in the presence of different concentrations of pluronics. Differentiation efficiency was assessed by quantitative real-time polymerase chain reaction for determining expression messenger RNA levels and by immunocytostaining for determining the protein expression of odontogenic markers (ie, dentin sialoprotein, dentin matrix protein 1, bone morphogenic protein 2, bone morphogenic protein 7) by measuring alkaline phosphatase enzyme activity and lastly by von Kossa staining for determining mineralization. Results The results revealed for the first time that F68 has a great potential to boost odontogenic differentiation of hTGSCs. P85 was found to reduce cell viability during differentiation. F127 was nontoxic to hTGSCs but did not have any effect on differentiation. Conclusions The positive effect of F68 on odontogenic differentiation might enable more efficient pulp regeneration. Yet, the exact mechanism of how F68 alters the differentiation pattern of hTGSCs remains to be investigated in the future studies.
机译:引言牙髓工程学的主要挑战是成功地将干细胞与生物材料结合起来,以期将干细胞分化为成牙细胞类型。在生物材料中,据报道某些类型的普朗尼克可增加干细胞的骨形成。这些pluronics对牙源性分化的影响尚未解决。这项研究旨在检查普朗尼克斯F68,F127和P85对源自年轻人第三磨牙牙胚的干细胞的牙源性分化的影响。方法在不同浓度的普卢尼克酮存在下,诱导人牙胚干细胞(hTGSCs)分化为成牙细胞。通过定量实时聚合酶链反应确定表达信使RNA水平并通过免疫细胞染色确定牙源性标记物(即牙本质唾液蛋白,牙本质基质蛋白1,骨形态发生蛋白2,骨形态发生蛋白7)的蛋白质表达来评估分化效率。通过测量碱性磷酸酶的活性,最后通过冯·科萨(von Kossa)染色确定矿化度。结果结果首次揭示F68具有促进hTGSCs牙源性分化的巨大潜力。发现P85在分化过程中降低了细胞活力。 F127对hTGSCs无毒,但对分化没有任何影响。结论F68对牙源性分化的积极作用可能使牙髓再生更有效。然而,F68如何改变hTGSCs分化模式的确切机制仍有待进一步研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号