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A thermoresponsive polydiolcitrate-gelatin scaffold and delivery system mediates effective bone formation from BMP9-transduced mesenchymal stem cells

机译:热响应性聚柠檬酸-明胶支架和递送系统介导BMP9转导的间充质干细胞有效形成骨

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Successful bone tissue engineering requires at the minimum sufficient osteoblast progenitors, efficient osteoinductive factors, and biocompatible scaffolding materials. We previously demonstrated that bone morphogenetic protein 9 (BMP9) is one of the most potent factors in inducing osteogenic differentiation of mesenchymal stem cells (MSCs). Here, we investigated the potential use of a biodegradable citrate-based thermosensitive macromolecule, poly(polyethyleneglycol citrateco-N-isopropylacrylamide) (PPCN) mixed with gelatin (PPCNG) as a scaffold for the delivery of BMP9-stimulated MSCs to promote localized bone formation. The addition of gelatin to PPCN effectively enhanced the cell adhesion and survival properties of MSCs entrapped within the gel in 3D culture. Using the BMP9-transduced MSC line immortalized mouse embryonic fibroblasts (iMEFs), we found that PPCNG facilitated BMP9-induced osteogenic differentiation of iMEFs in vivo and promoted the formation of well-ossified and vascularized trabecular bone-like structures in a mouse model of ectopic bone formation. Histologic evaluation revealed that vascularization of the bony masses retrieved from the ilVIEFs + PPCNG group was significantly more pronounced than that of the direct cell injection group. Accordingly, vascular endothelial growth factor (VEGF) expression was shown to be significantly higher in the bony masses recovered from the iMEFs + PPCNG group. Taken together, our results suggest that PPCNG may serve as a novel biodegradable and injectable scaffold and carrier for gene and cell-based bone tissue engineering.
机译:成功的骨组织工程至少需要足够的成骨细胞祖细胞,有效的骨诱导因子和生物相容性支架材料。我们以前证明骨形态发生蛋白9(BMP9)是诱导间充质干细胞(MSCs)成骨分化的最有效因素之一。在这里,我们调查了可生物降解的基于柠檬酸盐的热敏大分子,聚(聚乙二醇柠檬酸酯-N-异丙基丙烯酰胺)(PPCN)与明胶(PPCNG)混合作为支架的潜在用途,该支架可用于递送BMP9刺激的MSC,以促进局部骨形成。向PPCN中添加明胶可有效增强3D培养中凝胶中截留的MSC的细胞粘附性和存活特性。使用BMP9转导的MSC系永生小鼠胚胎成纤维细胞(iMEFs),我们发现PPCNG促进BMP9诱导的iMEFs体内成骨分化,并促进异位小鼠模型中骨化和血管化的小梁骨样结构的形成骨形成。组织学评估显示,从ilVIEFs + PPCNG组取回的骨块的血管形成明显比直接细胞注射组更明显。因此,在从iMEFs + PPCNG组中恢复的骨质中,血管内皮生长因子(VEGF)的表达被证明明显更高。两者合计,我们的结果表明,PPCNG可以作为一种新型的可生物降解和可注射的支架和载体,用于基因和基于细胞的骨组织工程。

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