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首页> 外文期刊>Experimental Biology and Medicine: Journal of the Society for Experimental Biology and Medicine >Repair of bone defects using a new biomimetic construction fabricated by adipose-derived stem cells, collagen I, and porous beta-tricalcium phosphate scaffolds
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Repair of bone defects using a new biomimetic construction fabricated by adipose-derived stem cells, collagen I, and porous beta-tricalcium phosphate scaffolds

机译:使用由脂肪干细胞,胶原蛋白I和多孔β-磷酸三钙支架制成的新型仿生结构修复骨缺损

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Adipose derived stem cells (ASCs) with multilineage differentiation capacities have been demonstrated as an alternative cell candidate for in vitro and in vivo bone regeneration. This suggests that they may be a potential candidate to repair the bone defects. We attempted to demonstrate the use of new biomimetic constructions of undifferentiated rabbit adipose-derived stem cells (rASCs) with fully interconnected porous beta-tricalcium phosphate (β-TCP) scaffolds encapsulated by collagen I hydrogel in the regeneration of a critical-sized defect of rabbit radii. Critical-sized defects in the left radii of rabbits were prepared and inserted with rASCs/collagen I/β-TCP scaffold composites or collagen I/β-TCP scaffold composites. The results were evaluated by histology, radiographs, micro-CT, Emission Computed Tomography (ECT), fluorochrome labeling, western blot, and mechanical testing at 4, 8, and 12 weeks postsurgery. Twelve weeks after implantation, the defects were almost completely repaired as confirmed by the presence of the cortical bone and medullary cavity, which was evaluated through radiologic, histologic, and biomechanical examination. Biodegradation of the biomaterials may be attributed to extracellular liquid dissolution together with cell-mediated phagocytosis. Our study shows that a greater number of rASCs in the porous β-TCP scaffold encapsulated by collagen I gel enhanced osteogenesis in critical-sized defects. We hope to garner new insight into the engineering of rASCs-based bone tissue for clinical application.
机译:具有多谱系分化能力的脂肪衍生干细胞(ASC)已被证明是体外和体内骨骼再生的备选细胞候选物。这表明它们可能是修复骨缺损的潜在候选者。我们试图证明未分化的兔脂肪干细胞(rASCs)与胶原蛋白I水凝胶封装的完全互连的多孔β-磷酸三钙(β-TCP)支架的新型仿生构造在再生关键尺寸缺陷中的用途。兔子半径。制备兔左半径的临界大小的缺损,并插入rASCs /胶原蛋白I /β-TCP支架复合材料或胶原蛋白I /β-TCP支架复合材料。在术后4、8和12周通过组织学,放射线照相,显微CT,放射计算机断层扫描(ECT),荧光标记,蛋白质印迹和机械测试对结果进行评估。植入后十二周,通过影像学,组织学和生物力学检查评估了皮质骨和髓腔的存在,证实了缺损几乎已完全修复。生物材料的生物降解可归因于细胞外液体溶解以及细胞介导的吞噬作用。我们的研究表明,胶原蛋白I凝胶包裹的多孔β-TCP支架中的大量rASC增强了关键尺寸缺损的成骨作用。我们希望对基于rASCs的骨组织工程化应用获得新的见识,以用于临床应用。

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