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A simple method for deriving functional MSCs and applied for osteogenesis in 3D scaffolds

机译:一种简单的获得功能性MSC的方法并应用于3D支架的成骨

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We describe a simple method for bone engineering using biodegradable scaffolds with mesenchymal stem cells derived from human induced-pluripotent stem cells (hiPS-MSCs). The hiPS-MSCs expressed mesenchymal markers (CD90, CD73, and CD105), possessed multipotency characterized by tri-lineages differentiation: osteogenic, adipogenic, and chondrogenic, and lost pluripotency – as seen with the loss of markers OCT3/4 and TRA-1-81 – and tumorigenicity. However, these iPS-MSCs are still positive for marker NANOG. We further explored the osteogenic potential of the hiPS-MSCs in synthetic polymer polycaprolactone (PCL) scaffolds or PCL scaffolds functionalized with natural polymer hyaluronan and ceramic TCP (PHT) both in vitro and in vivo . Our results showed that these iPS-MSCs are functionally compatible with the two 3D scaffolds tested and formed typically calcified structure in the scaffolds. Overall, our results suggest the iPS-MSCs derived by this simple method retain fully osteogenic function and provide a new solution towards personalized orthopedic therapy in the future.
机译:我们描述了一种可生物降解的支架与人类诱导多能干细胞(hiPS-MSCs)衍生的间充质干细胞的骨工程简单方法。 hiPS-MSC表达间充质标记(CD90,CD73和CD105),具有以三谱系分化为特征的多能性:成骨性,成脂性和成软骨性,以及丧失多能性-如丧失OCT3 / 4和TRA-1标记所见-81 –和致瘤性。但是,这些iPS-MSC仍对标记NANOG呈阳性。我们进一步探索了hiPS-MSC在合成聚合物聚己内酯(PCL)支架或天然聚合物透明质酸和陶瓷TCP(PHT)功能化的PCL支架中的成骨潜力。我们的结果表明,这些iPS-MSC与两个3D支架在功能上兼容,并且在支架中形成了典型的钙化结构。总体而言,我们的结果表明,通过这种简单方法衍生的iPS-MSC保留了完全的成骨功能,并为将来的个性化骨科治疗提供了新的解决方案。

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