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首页> 外文期刊>Journal of biomedical materials research, Part A >Chondrogenic differentiation of human mesenchymal stem cell aggregates via controlled release of TGF-β1 from incorporated polymer microspheres
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Chondrogenic differentiation of human mesenchymal stem cell aggregates via controlled release of TGF-β1 from incorporated polymer microspheres

机译:TGF-β1从掺入的聚合物微球中的受控释放,使人间充质干细胞聚集体的软骨分化

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Aggregate culture is a useful method for inducing chondrogenic differentiation of human mesenchymal stem cells (hMSC) in a three-dimensional in vitro culture environment. Conventional aggregate culture, however, typically requires repeated growth factor supplementation during media changes, which is both expensive and time-intensive. In addition, homogenous cell differentiation is limited by the diffusion of chondrogenic growth factor from the culture medium into the aggregate and peripheral cell consumption of the growth factor. We have engineered a technology to incorporate growth factor-loaded polymer microspheres within hMSC aggregates themselves. Here, we report on the system's capacity to induce chondrogenesis via sustained delivery of transforming growth factor-b1 (TGF-β1). Cartilage formation after 3 weeks in the absence of externally supplied growth factor approached that of aggregates cultured by conventional methods. Chondrogenesis in the central region of the aggregates is enabled at TGF-β1 levels much lower than those required by conventional culture using exogenously supplied TGF-β1, which is likely a result of the system's ability to overcome limitations of growth factor diffusion from cell culture media surrounding the exterior of the aggregates. Importantly, the inclusion of growth factor-releasing polymer microspheres in hMSC aggregates could enable in vivo chondrogenesis for cartilage tissue engineering applications without extensive in vitro culture.
机译:聚集培养是在三维体外培养环境中诱导人间充质干细胞(hMSC)软骨分化的有用方法。然而,常规的聚集培养通常需要在培养基更换期间重复补充生长因子,这既昂贵又费时。另外,均质细胞分化受到软骨生长因子从培养基扩散到生长因子的聚集体和外周细胞消耗中的限制。我们设计了一种技术,可以将负载生长因子的聚合物微球整合到hMSC聚集体自身中。在这里,我们报告了该系统通过持续传递转化生长因子-b1(TGF-β1)诱导软骨形成的能力。在没有外部供应的生长因子的情况下3周后的软骨形成接近通过常规方法培养的聚集体的软骨形成。聚集体中心区域的软骨形成能够在TGF-β1水平下大大低于使用外源供应的TGF-β1进行常规培养所需要的水平,这很可能是系统克服了生长因子从细胞培养基中扩散的能力所致围绕骨料的外部。重要的是,在hMSC聚集体中包含释放生长因子的聚合物微球可以实现软骨组织工程应用中的体内软骨形成,而无需大量的体外培养。

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