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Erythropoietin enhances osteogenic differentiation of human periodontal ligament stem cells via Wnt/β-catenin signaling pathway

机译:促红细胞生成素通过Wnt /β-catenin信号通路增强人牙周膜干细胞的成骨分化

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Objectives: The aim of this study is to examine the roles of erythropoietin (EPO) in regulating proliferation and osteogenic differentiation of periodontal ligament stem cells (PDLSCs) and analyze the underlying signaling of these processes. Materials and methods: PDLSCs were isolated and characterized. The PDLSCs were transfected with β-catenin shRNA. qRT-PCR and Western blot analysis were used to examine the osteogenic effects of EPO on the expression of osteogenic-related genes and protein (Runx2, OCN and Osterix) in PDLSCs. Alizarin Red-S staining was used to detect mineralized nodule formation. In addition, the relationship between the Wnt/β-catenin pathway and the effect of EPO on the osteogenesis of PDLSCs was investigated. Results: The results suggested that EPO exerts positive osteogenic effects on PDLSCs. The results showed that EPO decreased the growth of PDLSCs slightly and increased alkaline phosphatase activity and calcium deposition in a dose-dependent manner. The expression of Runx2, Osterix and OCN was increased after EPO administration. EPO increases β-catenin and Cyclin D1 in PDLSCs. After transfected with β-catenin shRNA, the osteogenic effect of EPO on PDLSCs was attenuated. Conclusion: EPO promotes osteogenic differentiation of PDLSCs. The underlying mechanism may be activating Wnt/β-catenin signaling pathway.
机译:目的:本研究的目的是检查促红细胞生成素(EPO)在调节牙周膜干细胞(PDLSC)的增殖和成骨分化中的作用,并分析这些过程的潜在信号传导。材料和方法:分离并鉴定了PDLSC。用β-连环蛋白shRNA转染PDLSC。使用qRT-PCR和Western blot分析来检查EPO对PDLSCs中成骨相关基因和蛋白质(Runx2,OCN和Osterix)表达的成骨作用。茜素红-S染色用于检测矿化的结节形成。此外,研究了Wnt /β-catenin途径与EPO对PDLSCs成骨作用的关系。结果:结果表明,EPO对PDLSCs具有积极的成骨作用。结果表明,EPO以剂量依赖的方式稍微降低了PDLSCs的生长,并增加了碱性磷酸酶的活性和钙的沉积。 EPO给药后,Runx2,Osterix和OCN的表达增加。 EPO增加PDLSCs中的β-catenin和Cyclin D1。用β-cateninshRNA转染后,EPO对PDLSC的成骨作用减弱。结论:EPO促进PDLSCs的成骨分化。潜在的机制可能是激活Wnt /β-catenin信号通路。

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