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TiO_2 nano-dimensioned surfaces modulate host inflammation via mediating macrophage M1/M2 polarization

机译:TiO_2纳米表面通过介导巨噬细胞M1 / M2极化来调节宿主炎症

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Small scale of nano-dimensioned TiO2 surface(NT5,30nm in diameter) help to maintain the static status of macrophage and to induce macrophage polarizing to anti-inflammatory M2 phenotype, which is benefit to inflammation resolution and bone regeneration. Manipulating nano-scales of surface topography can effectively regulate host innate inflammation and probably be a new strategy to improve performance of implanted biomaterials. However, additional research is still need to clarify the mechanism of surface-induced intracellular signal pathway.
机译:纳米尺寸的TiO2小表面(直径为NT5,30nm)有助于维持巨噬细胞的静态状态,并诱导巨噬细胞极化成抗炎M2表型,有利于炎症消退和骨骼再生。操纵纳米尺度的表面形貌可以有效调节宿主的先天性炎症,并且可能是提高植入生物材料性能的新策略。但是,仍然需要进一步的研究来阐明表面诱导的细胞内信号通路的机制。

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