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Polylactic Acid Nanopillar Array-Driven Osteogenic Differentiation of Human Adipose-Derived Stem Cells Determined by Pillar Diameter

机译:通过柱直径测定的人脂肪衍生的干细胞的聚乳酸纳米铝阵列驱动的骨质发生分化

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Numerous studies have determined that physical cues, especially the nanotopography of materials, play key roles in directing stem cell differentiation. However, most research on nanoarrays for stem cell fate regulation is based on nonbiodegradable materials, such as silicon wafers, TiO_(2), and poly(methyl methacrylate), which are rarely used as tissue engineering biomaterials. In this study, we prepared biodegradable polylactic acid (PLA) nanopillar arrays with different diameters but the same center-to-center distance using a series of anodic aluminum oxide nanowell arrays as templates. Human adipose-derived stem cells (hADSCs) were selected to investigate the effect of the diameter of PLA nanopillar arrays on stem cell differentiation. By culturing hADSCs without the assistance of any growth factors or osteogenic-induced media, the differentiation tendencies of hADSCs on the nanopillar arrays were assessed at the gene and protein levels. The assessment results suggested that the osteogenic differentiation of hADSCs can be driven by nanopillar arrays, especially by nanopillar arrays with a diameter of 200 nm. Moreover, an in vivo animal model of the samples demonstrated that PLA film with the 200 nm pillar array exhibits an improved ectopic osteogenic ability compared with the planar PLA film after 4 weeks of ectopic implantation. This study has provided a new variable to investigate in the interaction between stem cells and nanoarray structures, which will guide the bone regeneration clinical research field. This work paves the way for the utility of degradable biopolymer nanoarrays with specific geometrical and mechanical signals in biomedical applications, such as patches and strips for spine fusion, bone crack repair, and restoration of tooth enamel.
机译:许多研究已经确定了物理提示,尤其是材料的纳米复印件,在引导干细胞分化中发挥关键作用。然而,大多数关于干细胞命运调节的纳米阵列的研究基于非增生性材料,例如硅晶片,TiO_(2)和聚(甲基丙烯酸甲酯),其很少用作组织工程生物材料。在该研究中,我们制备了具有不同直径的可生物降解的聚乳酸(PLA)纳米玻璃阵列,但使用一系列阳极氧化铝纳米孔阵列作为模板,具有相同的中心到中心距离。选择人脂肪衍生的干细胞(HADSCs)以研究PLA纳米玻璃阵列直径对干细胞分化的影响。通过在没有任何生长因子或骨质发生培养基的辅助的情况下培养HADSCS,在基因和蛋白质水平评估纳米玻璃阵列上HADSCs的分化趋势。评估结果表明,HADSCs的骨质发生分化可以由纳米玻璃阵列驱动,尤其是直径为200nm的纳米玻璃阵列。此外,样品的体内动物模型证明,与200nm柱阵列的PLA膜与平面植入4周后的平面PLA膜相比具有改善的异位溶血能力。本研究提供了一种新的变量,用于研究干细胞和纳米阵列结构之间的相互作用,这将引导骨再生临床研究领域。这项工作为可降解的生物聚合物纳米阵列具有特定几何和机械信号的实用性铺平了生物医学应用中的特定几何和机械信号的方式,例如用于脊柱融合,骨裂纹修复和牙釉质恢复的斑块和条带。

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