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Culturing mouse embryonic stem cells with microcarriers in rotary cell culture system

机译:在旋转细胞培养系统中用微载体培养小鼠胚胎干细胞

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Embryonic stem cells (ESCs) hold promise either as an in vitro model recapitulating early embryonic development or as a renewable source of therapeutically useful cells. However, 2D culture system, which is still generally utilized in ESCs differentiation strategies, has greatly impeded our learning more information about ESCs proliferation/differentiation in situ. Here, a high aspect ratio vessel (HARV) was adopted to support mouse ESC culture due to its promising role in allowing more complex 3D tissue formation in vitro. An increased proliferation of ESCs in HARV was observed, in keeping with their enhanced metabolic activity. Moreover, supplement of the microcarriers significantly promoted ESCs assembling into macroscopic, tissue-like organoids during the culture. The ESCs lost their ¿stemness¿ property gradually as evidenced by their decreased expression level of undifferentiating markers over time. No significant difference of the time course of ESC differentiation was observed between the HARV and the static culture. However, an enhanced capability of their mesoderm and endoderm lineages differentiation was exhibited by the ESCs in HARV, in comparison with the static culture. We conclude that this HARV-ESC culture system might not only provide more information for the developmental biology in situ but also be directly used for tissue engineering research.
机译:胚胎干细胞(ESC)既可以作为概述早期胚胎发育的体外模型,也可以作为治疗有用细胞的可再生来源。但是,仍然在ESC分化策略中广泛使用的2D培养系统极大地阻碍了我们对ESC增殖/分化的更多信息的了解。在这里,由于采用了高纵横比容器(HARV)来支持小鼠ESC培养,这是因为它在体外允许更复杂的3D组织形成方面具有广阔的前景。观察到HARV中ESC的增殖增加,并与其代谢活性增强保持一致。此外,在培养过程中补充微载体可显着促进ESCs组装成宏观的组织样类器官。 ESC逐渐失去了它们的ƒƒâ€œstemnessââ€属性,这是由于随着时间的推移它们未分化标记的表达水平下降所证明的。在HARV和静态培养物之间未观察到ESC分化的时间过程的显着差异。然而,与静态培养相比,HARV中的ESC显示出其中胚层和内胚层谱系分化的能力增强。我们得出的结论是,这种HARV-ESC培养系统不仅可以为原位发育生物学提供更多信息,而且可以直接用于组织工程研究。

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