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Chondroitin Sulfate Microparticles Modulate Transforming Growth Factor-beta(1)-Induced Chondrogenesis of Human Mesenchymal Stem Cell Spheroids

机译:硫酸软骨素微粒调节人间充质干细胞球体的转化生长因子-β(1)诱导软骨生成。

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Mesenchymal stem cells (MSCs) have been previously explored as a part of cell-based therapies for the repair of damaged cartilage. Current MSC chondrogenic differentiation strategies employ large pellets; however, we have developed a technique to form small MSC aggregates (500-1,000 cells) that can reduce transport barriers while maintaining a multicellular structure analogous to cartilaginous condensations. The objective of this study was to examine the effects of incorporating chondroitin sulfate methacrylate (CSMA) microparticles (MPs) within small MSC spheroids cultured in the presence of transforming growth factor (TGF)-beta(1) on chondrogenesis. Spheroids with MPs induced earlier increases in collagen II and aggrecan gene expression (chondrogenic markers) than spheroids without MPs, although no large differences in immunostaining for these matrix molecules were observed by day 21 between these groups. Collagen I and X were also detected in the extracellular matrix (ECM) of all spheroids by immunostaining. Interestingly, histology revealed that CSMA MPs clustered together near the center of the MSC spheroids and induced circumferential alignment of cells and ECM around the material core. This study demonstrates the use of CSMA materials to further examine the effects of matrix molecules on MSC phenotype as well as potentially direct differentiation in a more spatially controlled manner that better mimics the architecture of specific musculoskeletal tissues. (C) 2014 S. Karger AG, Basel
机译:间充质干细胞(MSCs)以前已经作为细胞修复受损软骨的细胞疗法的一部分进行了研究。当前的MSC软骨分化策略采用大颗粒。然而,我们已经开发出一种形成小的MSC聚集体(500-1,000个细胞)的技术,它可以减少运输障碍,同时保持类似于软骨凝缩的多细胞结构。这项研究的目的是研究在转化生长因子(TGF)-beta(1)存在的情况下培养的小MSC球体中掺入硫酸软骨素甲基丙烯酸甲酯(CSMA)微粒(MPs)对软骨形成的影响。具有MP的球体诱导的胶原蛋白II和聚集蛋白聚糖基因表达(软骨生成标记)比无MP的球体更早地增加,尽管在第21天之前未观察到这些基质分子在免疫染色方面的大差异。还通过免疫染色在所有球体的细胞外基质(ECM)中检测到了胶原蛋白I和X。有趣的是,组织学发现CSMA MPs在MSC球体的中心附近聚集在一起,并引起细胞和ECM在材料核心周围的周向对齐。这项研究证明了使用CSMA材料进一步检查基质分子对MSC表型的影响以及以更受空间控制的方式更好地模仿特定肌肉骨骼组织结构的潜在直接分化。 (C)2014 S.Karger AG,巴塞尔

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