首页> 美国卫生研究院文献>Journal of Histochemistry and Cytochemistry >Spatial Distribution and Initial Changes of SSEA-1 and Other Cell Adhesion-related Molecules on Mouse Embryonic Stem Cells Before and During Differentiation
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Spatial Distribution and Initial Changes of SSEA-1 and Other Cell Adhesion-related Molecules on Mouse Embryonic Stem Cells Before and During Differentiation

机译:分化前后小鼠胚胎干细胞上SSEA-1和其他细胞粘附相关分子的空间分布和初始变化

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摘要

We examined the distribution of cell adhesion-related molecules (CAMs) among mouse embryonic stem (ES) cells and the spatial distribution on cell surfaces before and during differentiation. The cell-cell heterogeneity of SSEA-1, PECAM-1, and ICAM-1 among the undifferentiated cells in the ES cell colonies was evident by immunohistochemistry and immuno-SEM, supporting the flow cytometry findings. In contrast, most undifferentiated ES cells strongly expressed CD9. SSEA-1 was located preferentially on the edge of low protuberances and microvilli and formed clusters or linear arrays of 3–20 particles. PECAM-1 and ICAM-1 were randomly localized on the free cell surfaces, whereas CD9 was preferentially localized on the microvilli or protuberances, especially in the cell periphery. Both the SSEA-1+ fraction and the SSEA-1 fraction of magnetic cell sorting (MACS) formed undifferentiated colonies after plating. Flow cytometry showed that these populations reverted separately again to a culture with a mixed phenotype. Differentiation induced by retinoic acid downregulated the expression of all CAMs. Immuno-SEM showed decreases of SSEA-1 in the differentiated ES cells, although some clustering still remained. Our findings help to elucidate the significance of these molecules in ES cell maintenance and differentiation and suggest that cell surface antigens may be useful for defining the phenotype of undifferentiated and differentiated ES cells.
机译:我们检查了小鼠胚胎干(ES)细胞之间的细胞粘附相关分子(CAM)的分布以及分化之前和分化过程中细胞表面的空间分布。免疫组织化学和免疫-SEM证实了ES细胞集落中未分化细胞中SSEA-1,PECAM-1和ICAM-1的细胞异质性,支持流式细胞术的发现。相反,大多数未分化的ES细胞强烈表达CD9。 SSEA-1优先位于低隆起和微绒毛的边缘,并形成3-20个颗粒的簇或线性阵列。 PECAM-1和ICAM-1随机位于游离细胞表面,而CD9优先位于微绒毛或突起,特别是细胞外围。铺板后,磁性细胞分选(MACS)的SSEA-1 + 分数和SSEA-1 -分数均形成未分化的菌落。流式细胞仪显示,这些种群再次分别恢复为具有混合表型的培养物。维甲酸诱导的分化下调了所有CAM的表达。免疫SEM显示,分化的ES细胞中SSEA-1的减少,尽管仍然存在一些聚集。我们的发现有助于阐明这些分子在ES细胞维持和分化中的重要性,并暗示细胞表面抗原可能对确定未分化和分化ES细胞的表型有用。

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