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Distinct molecular basis for endothelial differentiation: Gene expression profiles of human mesenchymal stem cells versus umbilical vein endothelial cells

机译:内皮细胞分化的独特分子基础:人间充质干细胞与脐静脉内皮细胞的基因表达谱

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The capacity for endothelial differentiation has been described in mesenchymal stem cells (MSC) from human bone marrow. To identify genes associated with the endothelial differentiation potential of this cell-type, and search for the optimal regulatory factors, the expression profile of MSC was compared with cDNA from primary human umbilical vein endothelial cells as controls, using cDNA chips with 4096 genes. The data were corroborated by quantitative PCR, Western blotting, and immunocytochemistry. Among the 3948 effective genes, ~84% (3321) were co-expressed in both cell-types, and 627 were differentially expressed more than twofold in MSC versus EC. MSC highly expressed numerous stem-cell-like genes. Early development genes of endothelial cells, though not up-regulated, had a high expression in MSC, such as EDF1, MDG1, and EDG2. In contrast, mature endothelial growth and signal pathway genes, like VEGF, CXCR4, and CTNNB1, were down-regulated in MSC. In conclusion, human MSC have a distinct molecular basis for endothelial differentiation.
机译:在人骨髓的间充质干细胞(MSC)中已经描述了内皮分化的能力。为了鉴定与该细胞类型的内皮分化潜能相关的基因,并寻找最佳调节因子,使用具有4096个基因的cDNA芯片,将MSC的表达谱与人脐静脉内皮细胞的cDNA作对照。数据通过定量PCR,蛋白质印迹和免疫细胞化学得到证实。在3948个有效基因中,〜84%(3321)在两种细胞类型中共表达,并且627与MSC相比,EC差异表达两倍以上。 MSC高度表达了许多干细胞样基因。内皮细胞的早期发育基因尽管没有上调,但在MSC中具有高表达,例如EDF1,MDG1和EDG2。相反,成熟的内皮细胞生长和信号通路基因,例如VEGF,CXCR4和CTNNB1,在MSC中被下调。总之,人间充质干细胞具有内皮分化的独特分子基础。

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