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首页> 外文期刊>Cell transplantation >Bone Marrow Mesenchymal Stem Cells In a Three-DImensIonal Gelatin Sponge Scaffold Attenuate Inflammation, Promote Angiogenesis, and Reduce Cavity Formation In Experimental Spinal Cord Injury
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Bone Marrow Mesenchymal Stem Cells In a Three-DImensIonal Gelatin Sponge Scaffold Attenuate Inflammation, Promote Angiogenesis, and Reduce Cavity Formation In Experimental Spinal Cord Injury

机译:三维离子明胶海绵支架中的骨髓间充质干细胞减轻炎症,促进血管生成并减少实验性脊髓损伤中的腔形成。

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Three-dimensional (3D) gelatin sponge (GS) scaffolds were constructed by ensheathing GS with a thin film of poly-(lactide-co-glycolide) (PLGA). Rat bone marrow-derived mesenchymal stem cells (MSCs) were isolated, cultured, and then seeded to the scaffolds. Distribution of cells and cell growth, survival, and proliferation within the scaffolds were then determined. Immunofluorescence and Western blot analysis were employed to detect the deposition of fibronectin to the scaffolds on day 3 and day 7 of culture. Scaffolds with or without MSCs were then transplanted into the transected rat spinal cord. One or 8 weeks following transplantation, cavity areas, activated macrophages/microglia, expression of TNF-alpha and IL-1beta, and neovas-cularization within the grafts were examined and quantified. Deposition of fibronectin (FN) and expression of vascular endothelial growth factor (VEGF) and hypoxia-inducible factor-1alpha (HIF-1alpha) as potential inducing factors for angiogenesis were also examined. Results showed that 3D GS scaffolds allowed MSCs to adhere, survive, and proliferate and also FN to deposit. In vivo transplantation experiments demonstrated that these scaffolds were biocompatible, and MSCs seeded to the scaffolds played an important role in attenuating inflammation, promoting angiogenesis, and reducing cavity formation. Therefore, the GS scaffolds with MSCs may serve as promising supporting transplants for repairing spinal cord injury.
机译:三维(3D)明胶海绵(GS)支架是通过在GS上包裹一层聚丙交酯-乙交酯共聚物(PLGA)薄膜而制成的。分离,培养大鼠骨髓来源的间充质干细胞(MSCs),然后接种到支架上。然后确定支架内细胞的分布以及细胞生长,存活和增殖。在培养的第3天和第7天,采用免疫荧光和蛋白质印迹分析来检测纤连蛋白在支架上的沉积。然后将具有或不具有MSC的支架移植到横切的大鼠脊髓中。移植后一或八周,检查并定量移植腔内的面积,活化的巨噬细胞/小胶质细胞,TNF-α和IL-1beta的表达以及新生血管的形成。还检查了纤连蛋白(FN)的沉积以及血管内皮生长因子(VEGF)和缺氧诱导因子-1α(HIF-1alpha)的表达作为血管生成的潜在诱导因子。结果显示3D GS支架可使MSC粘附,存活和增殖,并使FN沉积。体内移植实验表明,这些支架具有生物相容性,接种在支架上的MSC在减轻炎症,促进血管生成和减少腔形成方面起着重要作用。因此,具有MSC的GS支架可以作为修复脊髓损伤的有希望的支持移植物。

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