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Transient Growth Factor Stimulation Improves Chondrogenesis in Static Culture and Under Dynamic Conditions in a Novel Shear and Perfusion Bioreactor

机译:瞬时生长因子刺激改善了新型剪切和灌注生物反应器中静态培养和动态条件下的软骨形成。

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摘要

Tissue engineering emerges as a viable method to replace cartilage damaged by osteoarthritis or trauma. A key element for cartilage tissue engineering is to elucidate growth factor exposure regimes that enhance cartilage production from multipotent progenitor cells. To address this, we identify growth factor conditions that promote chondrogenesis of human mesenchymal stem cells cultured under static conditions. We identified transient exposure to bone morphogenic protein-2 in the presence of transforming growth factor beta-1 as a viable condition that promotes expression of chondrogenic phenotype for human mesenchymal stem cells seeded onto polycaprolactone scaffolds. We then use this growth factor regime as a proof of concept to test a new shear and perfusion bioreactor. This novel bioreactor design applies shear stress stimulation on the surface of constructs while allowing tissue perfusion. Constructs harvested from the bioreactor after 8 days showed cartilage development primarily near the construct surface exposed to shear stress. By day 14, cells, collagen deposition and proteoglycan deposition is observed throughout the scaffold, indicative of cartilage development.
机译:组织工程学是替代因骨关节炎或创伤而受损的软骨的可行方法。软骨组织工程的关键要素是阐明可增强多能祖细胞产生软骨的生长因子暴露方案。为了解决这个问题,我们确定了促进在静态条件下培养的人间充质干细胞软骨形成的生长因子条件。我们发现在存在转化生长因子β-1的情况下,短暂暴露于骨形态发生蛋白2是一种可行的条件,该条件可以促进播种到聚己内酯支架上的人间充质干细胞的软骨表型表达。然后,我们使用该生长因子方案作为概念验证,以测试新的剪切和灌注生物反应器。这种新颖的生物反应器设计可在组织表面施加剪切应力刺激,同时允许组织灌注。 8天后从生物反应器收获的构建体显示出软骨发育主要在暴露于剪切应力的构建体表面附近。到第14天,在整个支架上观察到细胞,胶原蛋白沉积和蛋白聚糖沉积,表明软骨发展。

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