用仿生电纺丝纤维蛋白原纳米纤维和脂肪来源的间充质干细胞模拟早期骨再生

Michael P. Francis, Yas M. Moghaddam-White, Patrick C. Sachs, M. Beckman, Stephen M. Chen, G. Bowlin, L. Elmore, S. Holt
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引用次数: 5

摘要

骨再生早期阶段的关键事件已经在体内描述,尽管尚未在体外环境中建模,在体外环境中可以更有效地研究细胞基质-生长因子相互作用的机制。在这里,我们探索了早期骨再生模型,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发生的能力。将Fg、聚二氧环酮(PDO)和Fg:PDO混合物的电纺丝支架与脂肪来源的间充质干细胞(ASCs)相结合,在成骨分化培养基或对照生长培养基中培养7-21天。每周对支架进行成骨细胞发生的组织学和分子证据分析。在成骨分化培养基的作用下,植于Fg支架上的ASCs表现出与成骨细胞发生相关的多种基因的表达升高。组织学染色和扫描电镜显示支架内广泛的矿化,以及从头合成I型胶原蛋白。我们的数据表明,静电纺Fg纳米纤维支持ASC成骨分化,但支架本身似乎不具有成骨诱导作用。ASCs和Fg共同概括了体外骨再生的早期阶段,并为骨修复提供了一种前瞻性的自体治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modeling early stage bone regeneration with biomimetic electrospun fibrinogen nanofibers and adipose-derived mesenchymal stem cells
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.
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