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Nanotopographical induction of osteogenesis through adhesion, bone morphogenic protein co-signaling and regulation of microRNAs

机译:通过粘附,骨形态发生蛋白共信号传导和微小RNa的调节纳米形成诱导骨生成

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摘要

It is emerging that nanotopographical information can be used to induce osteogenesis from mesenchymal stromal cells from the bone marrow and it is hoped that this nanoscale bioactivity can be utilized to engineer next generation implants. However, the osteogenic mechanism of surfaces is currently poorly understood. In this report, we investigate mechanism and implicate bone morphogenic protein (BMP) in up-regulation of RUNX2 and show that RUNX2 and its regulatory miRNAs are BMP sensitive. Our data demonstrates that osteogenic nanotopography promotes co-localization of intergrins and BMP2 receptors in order to enhance osteogenic activity and that vitronectin is important in this interface. This provides insight that topographical regulation of adhesion can have effects on signaling cascades outside of cytoskeletal signaling and that adhesions can have roles in augmenting BMP signaling.
机译:新兴的纳米形貌信息可用于诱导骨髓间充质基质细胞的成骨作用,并希望这种纳米级的生物活性可用于工程化下一代植入物。但是,目前对表面的成骨机制了解甚少。在本报告中,我们研究了机制和暗示骨形态发生蛋白(BMP)上调RUNX2,并表明RUNX2及其调节性miRNA对BMP敏感。我们的数据表明,成骨纳米形貌可促进整合素和BMP2受体的共定位,以增强成骨活性,而玻连蛋白在该界面中很重要。这提供了洞察力,即粘附的形貌调节可以影响细胞骨架信号传导以外的信号传导级联,并且粘附可以在增强BMP信号传导中发挥作用。

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