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Novel chitosan/collagen scaffold containing transforming growth factor-beta 1 DNA for periodontal tissue engineering

机译:新型壳聚糖/胶原蛋白支架,包含用于牙周组织工程的转化生长因子-β1DNA

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The current rapid progression in tissue engineering and local gene delivery system has enhanced our applications to periodontal tissue engineering. In this study, porous chitosan/collagen scaffolds were prepared through a freeze-drying process, and loaded with plasmid and adenoviral vector encoding human transforming growth factor-beta 1 (TGF-beta 1). These scaffolds were evaluated in vitro by analysis of microscopic structure, porosity, and cytocompatibility. Human periodontal ligament cells (HPLCs) were seeded in this scaffold, and gene transfection could be traced by green fluorescent protein (GFP). The expression of type I and type III collagen was detected with RTPCR, and then these scaffolds were implanted subcutaneously into athymic mice. Results indicated that the pore diameter of the genecombined scaffolds was lower than that of pure chitosan/collagen scaffold. The scaffold containing Ad-TGF-beta 1 exhibited the highest proliferation rate, and the expression of type I and type III collagen up-regulated in Ad-TGF-beta 1 scaffold. After implanted in vivo, EGFP-transfected HPLCs not only proliferated but also recruited surrounding tissue to grow in the scaffold. This study demonstrated the potential of chitosan/collagen scaffold combined Ad-TGF-beta 1 as a good substrate candidate in periodontal tissue engineering. (c) 2006 Elsevier Inc. All rights reserved.
机译:当前组织工程和局部基因递送系统的快速发展增强了我们在牙周组织工程中的应用。在这项研究中,多孔壳聚糖/胶原蛋白支架是通过冷冻干燥过程制备的,并装有质粒和编码人转化生长因子-β1(TGF-β1)的腺病毒载体。通过分析微观结构,孔隙率和细胞相容性,体外评估了这些支架。将人牙周膜细胞(HPLC)接种在该支架中,并通过绿色荧光蛋白(GFP)追踪基因转染。用RTPCR检测I型和III型胶原的表达,然后将这些支架皮下植入无胸腺小鼠中。结果表明,基因组合支架的孔径小于纯壳聚糖/胶原支架的孔径。含有Ad-TGF-beta 1的支架表现出最高的增殖率,并且Ad-TGF-beta 1支架中I型和III型胶原的表达上调。体内植入后,转染EGFP的HPLC不仅增殖,而且募集周围组织以在支架中生长。这项研究表明壳聚糖/胶原蛋白支架结合Ad-TGF-beta 1作为牙周组织工程中良好的底物候选物的潜力。 (c)2006 Elsevier Inc.保留所有权利。

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