首页> 美国卫生研究院文献>Mediators of Inflammation >ET-1 Promotes Differentiation of Periodontal Ligament Stem Cells into Osteoblasts through ETR MAPK and Wnt/β-Catenin Signaling Pathways under Inflammatory Microenvironment
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ET-1 Promotes Differentiation of Periodontal Ligament Stem Cells into Osteoblasts through ETR MAPK and Wnt/β-Catenin Signaling Pathways under Inflammatory Microenvironment

机译:ET-1在炎性微环境下通过ETRMAPK和Wnt /β-Catenin信号通路促进牙周膜干细胞向成骨细胞的分化

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摘要

Periodontitis is a kind of chronic inflammatory disease that affects the tooth-supporting tissues. ET-1 is related to periodontitis and involved in the regulation of cytokines, but the mechanisms remain unclear. The aim of this study is to investigate how ET-1 affects proinflammatory cytokine expression and differentiation in human periodontal ligament stem cells (PDLSCs). PDLSCs were isolated from the periodontal ligament tissues of periodontitis patients and then treated with ET-1 (1, 10, or 100 nM) for 12 h, 24 h, or 72 h. The osteogenic potential of PDLSCs was tested using ALP staining. TNF-α, IL-1β, and IL-6 levels were evaluated by ELISA and western blot. Runx2, OCN, and COL1 mRNA and western levels were detected by RT-PCR and western blot, respectively. To examine the signaling pathways and molecular mechanisms involved in ET-1-mediated cytokine expression and osteogenic differentiation, ETR pathway, MAPKs pathway, Wnt/β-catenin pathway, and Wnt/Ca2+ pathway were detected by RT-PCR and western blot, respectively. ET-1 promoted differentiation of PDLSCs into osteoblasts by increasing secretion of TNF-α, IL-1β, and IL-6 in a dose- and time-dependent manner. ET-1 also increased expression of Runx2, OCN, and COL1. ET-1 promotes differentiation of PDLSCs into osteoblasts through ETR, MAPK, and Wnt/β-catenin signaling pathways under inflammatory microenvironment.
机译:牙周炎是一种影响牙齿支撑组织的慢性炎性疾病。 ET-1与牙周炎有关,并参与细胞因子的调节,但机制尚不清楚。这项研究的目的是研究ET-1如何影响人牙周膜干细胞(PDLSC)中的促炎细胞因子表达和分化。从牙周炎患者的牙周膜组织中分离出PDLSC,然后用ET-1(1、10或100 nM)处理12 forh,24 h或72 h。使用ALP染色测试了PDLSC的成骨潜力。通过ELISA和蛋白质印迹评估TNF-α,IL-1β和IL-6水平。分别通过RT-PCR和Western blot检测Runx2,OCN和COL1 mRNA和Western水平。为了检测ET-1介导的细胞因子表达和成骨分化的信号传导途径和分子机制,检测了ETR途径,MAPKs途径,Wnt /β-catenin途径和Wnt / Ca 2 + 途径分别通过RT-PCR和western blot。 ET-1通过以剂量和时间依赖性方式增加TNF-α,IL-1β和IL-6的分泌来促进PDLSCs向成骨细胞的分化。 ET-1还增加了Runx2,OCN和COL1的表达。在炎症微环境下,ET-1通过ETR,MAPK和Wnt /β-catenin信号通路促进PDLSCs向成骨细胞的分化。

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