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Stem Cell Surface Marker Expression Defines Late Stages of Reprogramming to Pluripotency in Human Fibroblasts

机译:干细胞表面标志物表达定义了人类成纤维细胞重编程为多能性的后期阶段

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Our Our current understanding of the induction of pluripotency by defined factors indicates that this process occurs in discrete stages characterized by specific alterations in the cellular transcriptome and epigenome. However, the final phase of the reprogramming process is incompletely understood. We sought to generate tools to characterize the transition to a fully reprogramed state. We used combinations of stem cell surface markers to isolate colonies emerging after transfection of human fibroblasts with reprogramming factors and then analyzed their expression of genes associated with pluripotency and early germ lineage specification. We found that expression of a subset of these genes, including the cell-cell adhesion molecule CDH3, characterized a late stage in the reprogramming process. Combined live-cell staining with the antibody GCTM-2 and anti-CDH3 during reprogramming identified colonies of cells that showed gene expression patterns very similar to those of embryonic stem cell or established induced pluripotent stem cell lines, and gave rise to stable induced pluripotent stem cell lines at high frequency. Our findings will facilitate studies of the final stages of reprogramming of human cells to pluripotency and will provide a simple means for prospective identification of fully reprogrammed cells.
机译:我们目前对定义因素诱导多能性的理解表明,该过程以细胞转录组和表观基因组的特定变化为特征的离散阶段发生。但是,重新编程过程的最后阶段尚不完全了解。我们试图生成工具来表征向完全重新编程状态的过渡。我们使用干细胞表面标志物的组合来分离用重编程因子转染人成纤维细胞后出现的菌落,然后分析它们与多能性和早期细菌谱系规格相关的基因表达。我们发现这些基因的一个子集的表达,包括细胞-细胞粘附分子CDH3,表征了重编程过程的后期。在重编程过程中,将活细胞染色与抗体GCTM-2和抗CDH3结合使用,可鉴定出细胞集落,这些集落的基因表达模式与胚胎干细胞或已建立的诱导多能干细胞系非常相似,并产生稳定的诱导多能干高频率的细胞系。我们的发现将有助于对人类细胞重编程为多能性的最终阶段进行研究,并将为前瞻性鉴定完全重编程的细胞提供简单的方法。

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