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Isolation and phenotypical characterization of mesenchymal stem cells from human fetal thymus.

机译:人胎胸腺间充质干细胞的分离和表型表征。

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摘要

Stem cells from human fetal thymus ectomesenchyma capable of forming colonies during in vitro culturing were isolated and characterized. Selection of culturing conditions showed that the growth and phenotypical characteristics of these cultures depended on seeding density and presence of basic fibroblast growth factor in the medium. After nonspecific inhibition of proliferation clonogenic cultures of thymic mesenchymal stem cells differentiated into myoblasts, formed characteristic myotubes, and expressed specific myogenesis markers. Colonies of thymic mesenchymal stem cells differentiated into chondrogenic, osteogenic, and adipogenic lines under conditions described for bone marrow mesenchymal stem cells. Cytofluorometric analysis of surface epitopes of thymic mesenchymal stem cells showed that the majority of cells expressed mesenchymal markers Thy-1, CD44, and CD105. Testing for CD34, CD38, CD45, and HLA-DR were negative in all cases. The main cell population (70-95%) did not express MHCl antigens during long-term culturing.
机译:分离并鉴定了在体外培养过程中能够形成菌落的人胎儿胸腺外间充质干细胞。选择培养条件表明,这些培养物的生长和表型特征取决于培养基中的接种密度和碱性成纤维细胞生长因子的存在。在非特异性抑制增殖后,胸腺间充质干细胞的克隆形成培养物分化为成肌细胞,形成特征性肌管,并表达特定的成肌标记。在针对骨髓间充质干细胞描述的条件下,胸腺间充质干细胞集落分化为软骨形成,成骨和成脂细胞系。胸腺间充质干细胞表面表位的细胞荧光分析表明,大多数细胞表达间充质标记物Thy-1,CD44和CD105。在所有情况下,CD34,CD38,CD45和HLA-DR的检测均为阴性。在长期培养过程中,主要细胞群(70-95%)不表达MHCl抗原。

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