首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Effects of Platelet-rich Plasma and Cell Coculture on Angiogenesis in Human Dental Pulp Stem Cells and Endothelial Progenitor Cells
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Effects of Platelet-rich Plasma and Cell Coculture on Angiogenesis in Human Dental Pulp Stem Cells and Endothelial Progenitor Cells

机译:富血小板血浆和细胞共培养对人牙髓干细胞和内皮祖细胞血管生成的影响

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Introduction: Platelet-rich plasma (PRP) has been described as platelet concentrate. Growth factors released by activated platelets can improve wound vasculogenesis and enhance wound healing. In this study, we used PRP instead of serum to culture human dental pulp stem cells (hDPSCs) and endothelial progenitor cells (EPCs) and investigated revascularization ability. The effect of hDPSC and EPC coculture on vasculogenesis was also studied. Methods: PRP was prepared by secondary centrifugation. Real-time polymerase chain reaction and Western blotting were used to determine the expression of vasculogenesis-related factors vascular growth factor, fetal liver kinase 1 (Flk-1), and stromal cell-derived factor 1 (SDF-1) in cultured hDPSCs and EPCs. The cells were divided into 4 groups: EPCs + 10% fetal bovine serum (FBS), EPCs + 10% PRP, EPCs + hDPSCs + 10% FBS, and EPCs + hDPSCs + 10% PRP. Then, the formation of vessel-like structures was tested by the tube formation assay. Results: On day 3, the expression levels of all the markers in the coculture groups were much higher than in the single-culture groups and were also higher in the PRP groups compared with the FBS groups (P < .05), except for SDF-1. Expression levels were significantly higher in the experimental groups (EPCs + 10% PRP, EPCs + hDPSCs + 10% FBS, and EPCs + hDPSCs + 10% PRP) than in the control group (EPCs + 10% FBS) and in the PRP groups/coculture groups compared with the FBS groups/single-culture groups (P < .01). The tube formation assay showed the area of vessel-like structures formed by the PRP group to be larger than in the FBS group (P < .05). Conclusions: PRP and coculture can both promote vasculogenesis, and PRP can promote EPCs to form vessel-like structures.
机译:简介:富血小板血浆(PRP)被描述为浓缩血小板。活化的血小板释放的生长因子可以改善伤口的血管生成并增强伤口的愈合。在这项研究中,我们使用PRP代替血清来培养人牙髓干细胞(hDPSCs)和内皮祖细胞(EPC),并研究了血管重建的能力。还研究了hDPSC和EPC共培养对血管生成的影响。方法:通过二次离心制备PRP。实时聚合酶链反应和Western印迹法用于确定血管生成相关因子血管生长因子,胎肝激酶1(Flk-1)和基质细胞衍生因子1(SDF-1)在培养的hDPSCs中的表达。 EPC。将细胞分为4组:EPCs + 10%胎牛血清(FBS),EPCs + 10%PRP,EPCs + hDPSCs + 10%FBS和EPCs + hDPSCs + 10%PRP。然后,通过管形成试验来测试血管状结构的形成。结果:在第3天,与FBS组相比,共培养组中所有标志物的表达水平均远高于单培养组,并且PRP组中所有标志物的表达水平也较高(P <.05)。 -1。实验组(EPCs + 10%PRP,EPCs + hDPSCs + 10%FBS和EPCs + hDPSCs + 10%PRP)的表达水平明显高于对照组(EPCs + 10%FBS)和PRP组/共培养组与FBS组/单一培养组相比(P <.01)。管形成试验显示,由PRP组形成的血管样结构的面积要大于FBS组(P <0.05)。结论:PRP和共培养均可促进血管生成,PRP可促进EPC形成血管样结构。

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