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The Role of Tantalum Nanoparticles in Bone Regeneration Involves the BMP2/Smad4/Runx2 Signaling Pathway

机译:钽纳米粒子在骨再生中的作用涉及BMP2 / SMAD4 / RUNX2信号通路

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Background: In recent years, nanomaterials have been increasingly developed and applied in the field of bone tissue engineering. However, there are few studies on the induction of bone regeneration by tantalum nanoparticles (Ta NPs) and no reports on the effects of Ta NPs on the osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and the underlying mechanisms. The main purpose of this study was to investigate the effects of Ta NPs on bone regeneration and BMSC osteogenic differentiation and the underlying mechanisms. Materials and Methods: The effects of Ta NPs on bone regeneration were evaluated in an animal experiment, and the effects of Ta NPs on osteogenic differentiation of BMSCs and the underlying mechanisms were evaluated in cell experiments. In the animal experiment, hematoxylin-eosin (HE) staining and hard-tissue section analysis showed that Ta NPs promoted bone regeneration, and immunohistochemistry revealed elevated expression of BMP2 and Smad4 in cells cultured with Ta NPs. Results: The results of the cell experiments showed that Ta NPs promoted BMSC proliferation, alkaline phosphatase (ALP) activity, BMP2 secretion and extracellular matrix (ECM) mineralization, and the expression of related osteogenic genes and proteins (especially BMP2, Smad4 and Runx2) was upregulated under culture with Ta NPs. Smad4 expression, ALP activity, ECM mineralization, and osteogenesis-related gene and protein expression decreased after inhibiting Smad4. Conclusion: These data suggest that Ta NPs have an osteogenic effect and induce bone regeneration by activating the BMP2/Smad4/Runx2 signaling pathway, which in turn causes BMSCs to undergo osteogenic differentiation. This study provides insight into the molecular mechanisms underlying the effects of Ta NPs in bone regeneration.
机译:背景:近年来,纳米材料越来越开发并应用于骨组织工程领域。然而,关于钽纳米颗粒(TA NPS)诱导骨再生的研究甚至没有关于Ta NP对骨髓间充质干细胞(BMSC)的骨质发生分化的影响的报道。本研究的主要目的是探讨TA NP对骨再生和BMSC成骨分化和潜在机制的影响。材料和方法:在动物实验中评估了Ta NP对骨再生的影响,并在细胞实验中评估了Ta NP对BMSCs和潜在机制的骨质发生分化的影响。在动物实验中,苏木精 - 曙红(HE)染色和硬组织截面分析表明,TA NPS促进了骨再生,免疫组织化学显示了与TA NP培养的细胞中BMP2和Smad4的升高。结果:细胞实验结果表明,TA NPS促进了BMSC增殖,碱性磷酸酶(ALP)活性,BMP2分泌和细胞外基质(ECM)矿化,以及相关骨质发生基因和蛋白质的表达(特别是BMP2,SMAD4和RUNX2)在用ta nps的培养下上调。 Smad4表达,ALP活性,ECM矿化和骨质发生相关基因和蛋白质表达在抑制Smad4后降低。结论:这些数据表明,TA NPS通过激活BMP2 / SMAD4 / RUNX2信号传导途径具有成骨效果并诱导骨再生,这反过来导致BMSC进行骨质发生分化。本研究介绍了对TA NPS在骨再生中的影响的分子机制的洞察力。

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