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Chondrogenic differentiation of human mesenchymal stem cells: a comparison between micromass and pellet culture systems

机译:人间充质干细胞的软骨分化:微质量和颗粒培养系统之间的比较

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High-density cell culture is pivotal for the chondrogenic differentiation of human mesenchymal stem cells (hMSCs). Two high-density cell culture systems, micromass and pellet culture, have been used to induce chondrogenic differentiation of hMSCs. In micromass culture, the induced-cartilage tissues were larger, more homogenous and enriched in cartilage-specific collagen II but the fibrocartilage-like feature, collagen I, and hypertrophic chondrocyte feature, collagen X, were markedly decreased compared to those in pellet culture. Furthermore, real time RT-PCR analysis demonstrated that collagen II and aggrecan mRNA were up-regulated while collagen X and collagen I mRNA were down-regulated in micromass culture. Thus, the micromass culture system is a promising tool for in vitro chondrogenic studies.
机译:高密度细胞培养对于人间充质干细胞(hMSCs)的软骨形成分化至关重要。两种高密度细胞培养系统,即微质量培养和沉淀培养已被用于诱导hMSC的软骨分化。在微团培养中,诱导的软骨组织更大,更均一且富含软骨特异性胶原II,但与粒团培养相比,纤维软骨样特征胶原I和肥大软骨细胞特征胶原X明显减少。此外,实时RT-PCR分析表明,在微团培养中,II型胶原和聚集蛋白聚糖的mRNA被上调,而X型胶原和I型胶原的mRNA被下调。因此,微质量培养系统是用于体外软骨形成研究的有前途的工具。

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