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首页> 外文期刊>Journal of tissue engineering and regenerative medicine >In vitro generation of a multilayered osteochondral construct with an osteochondral interface using rabbit bone marrow stromal cells and a silk peptide-based scaffold
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In vitro generation of a multilayered osteochondral construct with an osteochondral interface using rabbit bone marrow stromal cells and a silk peptide-based scaffold

机译:使用兔骨髓基质细胞和基于丝肽的支架体外产生具有骨软骨界面的多层骨软骨构建体

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摘要

Tissue engineering of a biological osteochondral multilayered construct with a cartilage-interface subchondral bone layer is a key challenge. This study presented a rabbit bone marrow stromal cell (BMSC)/silk fibroin scaffold-based co-culture approach to generate tissue-engineered osteochondral grafts with an interface. BMSC-seeded scaffolds were first cultured separately in osteogenic and chondrogenic stimulation media. The two differentiated pieces were then combined using an RADA self-assembling peptide and subsequently co-cultured. Gene expression, histological and biochemical analyses were used to evaluate the multilayered structure of the osteochondral graft. A complete osteochondral construct with a cartilage-subchondral bone interface was regenerated and BMSCs were used as the only cell source for the osteochondral construct and interface regeneration. Furthermore, in the intermediate region of co-cultured samples, hypertrophic chondrogenic gene markers type X collagen and MMP-13 were found on both chondrogenic and osteogenic section edges after co-culture. However, significant differences gene expression profile were found in distinct zones of the construct during co-culture and the section in the intermediate region had significantly higher hypertrophic chondrocyte gene expression. Biochemical analyses and histology results further supported this observation. This study showed that specific stimulation from osteogenic and chondrogenic BMSCs affected each other in this co-culture system and induced the formation of an osteochondral interface. Moreover, this system provided a possible approach for generating multilayered osteochondral constructs. Copyright (c) 2013 John Wiley & Sons, Ltd.
机译:具有软骨界面软骨下骨层的生物骨软骨多层构建体的组织工程设计是一项关键挑战。这项研究提出了一种基于兔骨髓基质细胞(BMSC)/丝素蛋白支架的共培养方法,以产生具有界面的组织工程骨软骨移植物。首先将BMSC接种的支架分别在成骨和成软骨刺激培养基中培养。然后使用RADA自组装肽将两个分化的片段合并,然后共培养。基因表达,组织学和生化分析用于评估骨软骨移植物的多层结构。具有软骨-软骨下骨界面的完整的骨软骨构建体被再生,并且BMSC被用作骨软骨构建体和界面再生的唯一细胞来源。此外,在共培养样品的中间区域,共培养后在软骨和成骨切片的边缘都发现了肥大的软骨生成基因标记物X型胶原和MMP-13。然而,在共培养期间,在构建体的不同区域中发现了显着差异的基因表达谱,并且中间区域中的部分具有明显更高的肥大软骨细胞基因表达。生化分析和组织学结果进一步支持了这一观察。这项研究表明,在这种共培养系统中,成骨和成软骨BMSC的特异性刺激相互影响,并诱导了骨软骨界面的形成。而且,该系统提供了产生多层骨软骨构造的可能方法。版权所有(c)2013 John Wiley&Sons,Ltd.

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