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Expansion of Human Articular Chondrocytes on Microcarriers Enhances the Production of Cartilage Specific Matrix Components

机译:对微括号的人关节软骨细胞的扩张增强了软骨特异性基质组分的生产

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Cell based technologies for the repair of cartilage defects usually rely on the expansion of low numbers of chondrocytes isolated from biopsies of healthy cartilage. Proliferating chondrocytes are known to undergo dedifferentiation which is characterised by down-regulation of collagen type II and proteoglycan production, and by up-regulation of collagen type I synthesis. Re-expression of cartilage specific matrix components by expanded chondrocytes is therefore critical for successful cartilage repair. In this study, it is shown that the quality of matrix synthesis by expanded chondrocytes is highly dependent on the method of expansion. Expanding human articular chondrocytes (HAC) on microcarriers without subcultivation steps leads to higher matrix synthesis rates and to superior ratios of collagen type II to type I forming cells than the expansion in conventional monolayer culture.
机译:基于细胞的软骨缺陷修复的技术通常依赖于从健康软骨的活组织检查中分离的低数量的软骨细胞。已知增殖软骨细胞经历过二草化,其特征在于胶原II型和蛋白多糖生产的下调,并通过胶原I型合成的上调。因此,通过扩张的软骨细胞再表达软骨特异性基质组分对成功的软骨修复至关重要。在本研究中,表明扩张的软骨细胞的基质合成的质量高度依赖于膨胀方法。在没有亚文化步骤的微载体上扩增人关节软骨细胞(HAC)导致较高的基质合成速率和胶原II型的优异比例,以型I型形成细胞比常规单层培养物中的膨胀。

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