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Modeling early stage bone regeneration with biomimetic electrospun fibrinogen nanofibers and adipose-derived mesenchymal stem cells

机译:用仿生电纺纤维蛋白原纳米纤维和脂肪间充质干细胞模拟早期骨再生

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Abstract > The key events of the earliest stages of bone regeneration have been described in vivo although not yet modeled in an in vitro environment, where mechanistic cell-matrix-growth factor interactions can be more effectively studied. Here, we explore an early-stage bone regeneration model where the ability of electrospun fibrinogen (Fg) nanofibers to regulate osteoblastogenesis between distinct mesenchymal stem cells populations is assessed. Electrospun scaffolds of Fg, polydioxanone (PDO), and a Fg:PDO blend were seeded with adipose-derived mesenchymal stem cells (ASCs) and grown for 7-21 days in osteogenic differentiation media or control growth media. Scaffolds were analyzed weekly for histologic and molecular evidence of osteoblastogenesis. In response to osteogenic differentiation media, ASCs seeded on the Fg scaffolds exhibit elevated expression of multiple genes associated with osteoblastogenesis. Histologic stains and scanning electron microscopy demonstrate widespread mineralization within the scaffolds, as well as de novo type I collagen synthesis. Our data demonstrates that electrospun Fg nanofibers support ASC osteogenic differentiation, yet the scaffold itself does not appear to be osteoinductive. Together, ASCs and Fg recapitulate early stages of bone regeneration ex vivo and presents a prospective autologous therapeutic approach for bone repair.
机译:摘要 >尽管尚未在体外环境中进行建模,但已在体内对骨再生最早阶段的关键事件进行了描述,在该环境中可以更有效地研究机械性的细胞-基质-生长因子相互作用。在这里,我们探索早期的骨再生模型,其中评估了电纺纤维蛋白原(Fg)纳米纤维调节不同间充质干细胞群体之间成骨细胞生成的能力。将Fg,聚二恶烷酮(PDO)和Fg:PDO共混物的电纺支架接种到脂肪来源的间充质干细胞(ASC)中,并在成骨分化培养基或对照生长培养基中生长7-21天。每周分析支架的成骨细胞学的组织学和分子学证据。响应成骨分化培养基,接种在Fg支架上的ASC显示出与成骨细胞相关的多个基因的表达升高。组织学染色和扫描电子显微镜显示支架内广泛的矿化以及从头开始的I型胶原合成。我们的数据表明,电纺Fg纳米纤维支持ASC成骨分化,但支架本身似乎没有骨诱导性。 ASC和Fg共同概述了离体骨再生的早期阶段,并提出了一种前瞻性自体骨修复治疗方法。

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