University of Liverpool, Clinical Engineering, School of Clinical Sciences, Liverpool, UK.
Biomaterials. 2010 May;31(15):4330-40. doi: 10.1016/j.biomaterials.2010.02.010.
Highly cellularised 3D-tissue constructs designed to repair large, complex abdominal wall defects were prepared using poly (lactic acid) (PLLA)-collagen scaffolds in vitro using a flow perfusion bioreactor. The PLLA-collagen scaffolds had a unique structure consisting of a collagen sponge formed within the pores of a mechanically stable knitted mesh of PLLA. The effect of the flow perfusion bioreactor culturing conditions was investigated in vitro for 0, 7, 14 and 28 days on scaffolds seeded with dermal fibroblasts. The cultured constructs were subsequently studied subcutaneously (SC) in an in vivo animal model. The results of in vitro studies demonstrated that the perfusion system facilitated increased cell proliferation and homogenous distribution in the PLLA-collagen scaffolds compared to static conditions. A highly cellularised 3D-tissue construct was formed by 7 days incubation under perfusion conditions, with increased cellularity by the 28 day time point. The in vivo model demonstrated that implanting constructs with high cellularity resulted in exceptional cell stabilisation, with the survival of implanted cells and expression of the phenotypically-relevant extracellular matrix proteins collagen types I and III, studied by fluorescence in situ hybridisation (FISH) and immunohistochemistry. The implantation of this porous PPLA-collagen scaffold seeded with dermal fibroblasts following in vitro maturation using a flow perfusion bioreactor system suggests a significant advance over current state-of-the-art procedures for the reconstruction of large, complex abdominal wall tissue defects.
采用聚乳酸(PLLA)-胶原支架,通过流灌培养生物反应器,在体外设计并制备了用于修复大型复杂腹壁缺损的高度细胞化 3D 组织构建体。PLLA-胶原支架具有独特的结构,由形成于机械稳定的 PLLA 编织网孔内的胶原海绵组成。体外研究了 0、7、14 和 28 天的流灌培养条件对成纤维细胞接种的支架的影响。随后将培养的构建体在体内动物模型中进行皮下(SC)研究。体外研究结果表明,与静态条件相比,灌注系统促进了细胞增殖和 PLLA-胶原支架中的均匀分布。在灌注条件下孵育 7 天即可形成高度细胞化的 3D 组织构建体,28 天时细胞数量增加。体内模型表明,植入高细胞密度的构建体可实现卓越的细胞稳定,植入细胞的存活以及细胞表型相关细胞外基质蛋白 I 型和 III 型胶原的表达,通过荧光原位杂交(FISH)和免疫组织化学进行研究。通过流灌培养生物反应器系统在体外成熟后,将这种多孔 PLLA-胶原支架与真皮成纤维细胞共培养,这对大型复杂腹壁组织缺损的重建提出了重大的技术进步。
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