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首页> 外文期刊>BioMed research international >Effects of Canonical NF-κB Signaling Pathway on the Proliferation and Odonto/Osteogenic Differentiation of Human Stem Cells from Apical Papilla
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Effects of Canonical NF-κB Signaling Pathway on the Proliferation and Odonto/Osteogenic Differentiation of Human Stem Cells from Apical Papilla

机译:规范性NF-κB信号通路对人根尖顶乳头干细胞增殖及牙本质/成骨分化的影响

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Background Information. NF-κB signaling pathway plays a complicated role in the biological functions of mesenchymal stem cells. However, the effects of NF-κB pathway on the odonto/osteogenic differentiation of stem cells from apical papilla (SCAPs) remain unclear. The present study was designed to evaluate the effects of canonical NF-κB pathway on the osteo/odontogenic capacity of SCAPsin vitro.Results. Western blot results demonstrated that NF-κB pathway in SCAPs was successfully activated by TNF-αor blocked by BMS-345541. NF-κB pathway-activated SCAPs presented a higher proliferation activity compared with control groups, as indicated by dimethyl-thiazol-diphenyl tetrazolium bromide assay (MTT) and flow cytometry assay (FCM). Wound scratch assay revealed that NF-κB pathway-activated SCAPs presented an improved migration capacity, enhanced alkaline phosphatase (ALP) activity, and upregulated mineralization capacity of SCAPs, as compared with control groups. Meanwhile, the odonto/osteogenic markers (ALP/ALP,RUNX2/RUNX2,OSX/OSX,OCN/OCN,OPN/OPN,BSP/BSP,DSPP/DSP, andDMP-1/DMP-1) in NF-κB pathway-activated SCAPs were also significantly upregulated as compared with control groups at both protein and mRNA levels. However, NF-κB pathway-inhibited SCAPs exhibited a lower proliferation/migration capacity, and decreased odonto/osteogenic ability in comparison with control groups.Conclusion. Our findings suggest that classical NF-κB pathway plays a paramount role in the proliferation and committed differentiation of SCAPs.
机译:背景信息。 NF-κB信号通路在间充质干细胞的生物学功能中起着复杂的作用。但是,尚不清楚NF-κB通路对顶突乳头(SCAPs)干细胞的牙本质/成骨分化的影响。本研究旨在评估经典NF-κB途径对SCAPs体外成骨/成牙能力的影响。 Western印迹结果表明,SCAPs中的NF-κB通路被TNF-α成功激活或被BMS-345541阻断。 NF-κB途径激活的SCAPs与对照组相比具有更高的增殖活性,如二甲基噻唑-二苯基溴化四氮唑测定法(MTT)和流式细胞术测定(FCM)所表明的。伤口刮伤试验显示,与对照组相比,NF-κB途径激活的SCAPs表现出更高的迁移能力,增强的碱性磷酸酶(ALP)活性以及上调的SCAPs矿化能力。同时,NF-κB途径中的牙本质/成骨标志物(ALP / ALP,RUNX2 / RUNX2,OSX / OSX,OCN / OCN,OPN / OPN,BSP / BSP,DSPP / DSP和DMP-1 / DMP-1)与对照组相比,活化的SCAPs在蛋白质和mRNA水平上也显着上调。然而,与对照组相比,NF-κB途径抑制的SCAPs具有较低的增殖/迁移能力,并降低了牙本质/成骨能力。我们的发现表明,经典的NF-κB途径在SCAP的增殖和定向分化中起着至关重要的作用。

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