首页> 外文期刊>Tissue engineering, Part A >Chondrogenic differentiation of human mesenchymal stem cells on oriented nanofibrous scaffolds: engineering the superficial zone of articular cartilage.
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Chondrogenic differentiation of human mesenchymal stem cells on oriented nanofibrous scaffolds: engineering the superficial zone of articular cartilage.

机译:定向纳米纤维支架上人间充质干细胞的软骨分化:工程化关节软骨的表层区域。

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摘要

Cell differentiation, adhesion, and orientation are known to influence the functionality of both natural and engineered tissues, such as articular cartilage. Several attempts have been devised to regulate these important cellular behaviors, including application of inexpensive but efficient electrospinning that can produce patterned extracellular matrix (ECM) features. Electrospun and oriented polycaprolactone (PCL) scaffolds (500 or 3000 nm fiber diameter) were created, and human mesenchymal stem cells (hMSCs) were cultured on these scaffolds. Cell viability, morphology, and orientation on the fibrous scaffolds were quantitatively determined as a function of time. While the fiber-guided initial cell orientation was maintained even after 5 weeks, cells cultured in the chondrogenic media proliferated and differentiated into the chondrogenic lineage, suggesting that cell orientation is controlled by the physical cues and minimally influenced by the soluble factors. Based on assessment by the chondrogenic markers, use of the nanofibrous scaffold (500 nm) appears to enhance the chondrogenic differentiation. These findings indicate that hMSCs seeded on a controllable PCL scaffold may lead to an alternate methodology to mimic the cell and ECM organization that is found, for example, in the superficial zone of articular cartilage.
机译:已知细胞分化,粘附和取向会影响天然和工程组织(例如关节软骨)的功能。已经设计出几种尝试来调节这些重要的细胞行为,包括应用廉价但有效的静电纺丝,该静电纺丝可以产生图案化的细胞外基质(ECM)特征。创建了电纺和定向的聚己内酯(PCL)支架(纤维直径为500或3000 nm),并在这些支架上培养了人间充质干细胞(hMSCs)。纤维支架上的细胞活力,形态和方向被定量确定为时间的函数。尽管在5周后仍保持了纤维引导的初始细胞方向,但在软骨形成培养基中培养的细胞增殖并分化为软骨形成谱系,这表明细胞方向受物理提示控制,而受可溶性因子的影响最小。根据软骨形成标记的评估,使用纳米纤维支架(500 nm)似乎可以增强软骨形成的分化。这些发现表明,在可控制的PCL支架上接种的hMSC可能导致模仿在关节软骨浅层发现的细胞和ECM组织的替代方法。

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