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Mesenchymal stromal/stem cell-or chondrocyte-seeded microcarriers as building blocks for cartilage tissue engineering

机译:间充质基质/干细胞或软骨细胞接种的微载体作为软骨组织工程的基础

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In this study we have tested the use of mesenchymal stromal/stem cell (MSC)- or chondrocyte (hch)-laden microcarriers as building blocks for engineered cartilage tissue. MSCs and hchs expanded on microcarriers were used in chondrogenic coculture and compared with monoculture of MSCs or hchs. The use of cell-laden microcarriers as building blocks for cartilage tissue engineering led to a compact tissue formation with significant volume increase compared to the biomaterial-free approach. After 28 days of differentiation culture, formation of cartilaginous matrix in cocultures and chondrocyte monoculture approaches was observed. Coculture resulted in beneficial glycosaminoglycan deposition compared with monoculture of MSCs or chondrocytes attached to microcarriers. Further, the microcarrier-adhered coculture displayed increased levels of the differentiation marker ACAN and reduced levels of the dedifferentiation marker COL1A1. To our knowledge, this is the first article that successfully combines an innovative combination of cell expansion on microcarriers and the direct use of MSC- or hch-cell-laden microcarriers as building blocks in cartilage tissue engineering.
机译:在这项研究中,我们测试了间充质基质/干细胞(MSC)或软骨细胞(hch)载有微载体作为工程软骨组织的基础。将在微载体上扩增的MSC和hchs用于软骨形成共培养,并与MSC或hchs的单培养进行比较。与不含生物材料的方法相比,使用载有细胞的微载体作为软骨组织工程的构建基块可以形成致密的组织,体积显着增加。分化培养28天后,在共培养和软骨细胞单培养方法中观察到了软骨基质的形成。与单细胞培养的MSC或附着在微载体上的软骨细胞相比,共培养可产生有益的糖胺聚糖沉积。此外,粘附有微载体的共培养物显示出分化标记物ACAN水平升高,而去分化标记物COL1A1水平降低。据我们所知,这是第一篇成功地将细胞在微载体上扩展的创新组合与直接使用载有MSC或hch细胞的微载体作为软骨组织工程的基础模块的成功结合。

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