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Characterization of mouse clonal mesenchymal stem cell lines established by subfractionation culturing method

机译:通过分级分离培养方法建立的小鼠克隆间充质干细胞系的表征

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摘要

AIM: To characterize single-cell-derived mouse clonal mesenchymal stem cells (mcMSCs) established with bone marrow samples from three different mouse strains.METHODS: We established mcMSC lines using subfractionation culturing method from bone marrow samples obtained from long bones. These lines were characterized by measuring cell growth, cell surface epitopes, differentiation potential, lineage-specific gene expression and T-cell suppression capability. Nonclonal MSCs isolated by the conventional gradient centrifugation method were used as controls.RESULTS: All mcMSC lines showed typical nonclonal MSC-like spindle shape morphology. Lines differed in optimal growth density requirement. Cell surface epitope profiles of these mcMSC lines were similar to those of nonclonal MSCs. However, some lines exhibited different expression levels in a few epitopes, such as CD44 and CD105. Differentiation assays showed that 90% of the mcMSC lines were capable of differentiating into adipogenic and/or chondrogenic lineages, but only 20% showed osteogenic lineage differentiation. T-cell suppression analysis showed that 75% of the lines exhibited T-cell suppression capability.CONCLUSION: mcMSC lines have similar cell morphology and cell growth rate but exhibit variations in their cell surface epitopes, differentiation potential, lineage-specific gene expression and T-cell suppression capability.
机译:目的:表征用来自三种不同小鼠品系的骨髓样品建立的单细胞源性小鼠骨髓间充质干细胞(方法)。方法:我们采用亚分级培养方法,从长骨骨髓样品中建立了mcMSC系。通过测量细胞生长,细胞表面表位,分化潜能,谱系特异性基因表达和T细胞抑制能力来表征这些细胞系。结果:所有mcMSC细胞系均表现出典型的非MSC样纺锤状形态。线在最佳生长密度要求上有所不同。这些mcMSC系的细胞表面抗原决定簇谱与非克隆MSC相似。但是,某些品系在一些表位上表现出不同的表达水平,例如CD44和CD105。分化测定表明,有90%的mcMSC系能够分化为成脂和/或成软骨谱系,但只有20%的细胞具有成骨谱系分化能力。 T细胞抑制分析表明,其中75%的品系具有T细胞抑制能力。结论:mcMSC品系具有相似的细胞形态和细胞生长速率,但其细胞表面表位,分化潜能,谱系特异性基因表达和T均存在差异-细胞抑制能力。

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