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Chondrogenic Differentiation of Human Mesenchymal Stem Cells During Multiple Subcultivation

机译:多重枢化期间人间充质干细胞的软糖分化

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The potential of human mesenchymal stem cells (hMSC) to differentiate into various types of mesenchymal tissue such as chondrocytes makes them a potential cell source in cartilage tissue engineering. Because of the requirement of high cell amounts for the generation of cartilage implants or for the extensive experimental studies to investigate the culture parameters the initial cells have to be expanded which leads to high population doubling numbers. It is known that hMSC can differentiate into chondrocytes at least up to the 15th population doubling. To monitor the differentiation status the protein MIA (melanoma inhibitory activity) which is only synthesized by malignant melanomas and chondrocytes can be used. In this study the chondrogenic differentiation potential of hMSC beyond the 15th population doubling was investigated using MIA as chondrocyte marker. A chondrogenic potential of hMSC at higher population doubling numbers may be of interest due to the requirement of less frequently isolations of cells. Therefore hMSC were cultured in monolayer until the 37th population doubling. Cells of different passages were cultured as pellets for two weeks in transforming growth factor (TGF)-B3 containing differentiation medium. The MIA contents in medium of the last three cultivation days in each case were measured using a MIA-ELISA-kit. A significant difference between MIA content in medium of pellet and non stimulated monolayer reference cultures could be detected until the 32nd population doubling. In addition the hMSC were seeded at lower densities to investigate whether the cells may be expanded faster and with less amount of work due to higher population doubling numbers per passage. The reduced inoculation density led to an increased growth rate.
机译:人间充质干细胞(HMSC)分化成各种类型的间充质组织如软骨细胞,使其成为软骨组织工程中的潜在细胞来源。由于对软骨植入物产生的高细胞量或进行了广泛的实验研究,以研究培养参数必须扩展初始细胞,这导致高人群倍增数。众所周知,HMSC可以至少分化为软骨细胞,至少达到第15次群体倍增。为了监测分化状态,可以使用仅通过恶性黑色素和软骨细胞合成的蛋白质MIA(黑色素瘤抑制活性)。在这项研究中,使用MIA作为软骨细胞标记,研究了超出第15次群体的HMSC的软骨性分化潜力。由于细胞不太隔离的要求,较高人群倍增数字在较高人口倍增数字下的HMSC的软骨潜力可能是有意义的。因此,HMSC在单层培养,直至第37次群体加倍。将不同通道的细胞培养为颗粒,在转化含生长因子(TGF)-B3的分化培养基中培养为颗粒2周。使用MIA-ELISA-套件测量每种情况下的最后三天培养日的培养基中的MIA含量。可以检测颗粒培养基中的MIA含量与非刺激的单层参考培养物之间的显着差异,直到32nd群体加倍。此外,在较低密度下接种HMSC以研究细胞是否可以更快地扩展,并且由于每篇文章的群体倍增数量较高,因此工作量较少。减少的接种密度导致增长率增加。

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