SOX2 Is Regulated Differently from NANOG and OCT4 in Human Embryonic Stem Cells during Early Differentiation Initiated with Sodium Butyrate

被引:25
|
作者
Kallas, Ade [1 ]
Pook, Martin [1 ]
Trei, Annika [1 ]
Maimets, Toivo [1 ]
机构
[1] Univ Tartu, Inst Mol & Cell Biol, EE-51010 Tartu, Estonia
关键词
HEPATOCYTE-LIKE CELLS; ISLET-LIKE CLUSTERS; EFFICIENT DIFFERENTIATION; HEPATIC ENDODERM; SELF-RENEWAL; GENERATION; MOUSE; PHOSPHORYLATION; PLURIPOTENCY; EXPRESSION;
D O I
10.1155/2014/298163
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Transcription factors NANOG, OCT4, and SOX2 regulate self-renewal and pluripotency in human embryonic stem (hES) cells; however, their expression profiles during early differentiation of hES cells are unclear. In this study, we used multiparameter flow cytometric assay to detect all three transcription factors (NANOG, OCT4, and SOX2) simultaneously at single cell level and monitored the changes in their expression during early differentiation towards endodermal lineage (induced by sodium butyrate). We observed at least four distinct populations of hES cells, characterized by specific expression patterns of NANOG, OCT4, and SOX2 and differentiation markers. Our results show that a single cell can express both differentiation and pluripotency markers at the same time, indicating a gradual mode of developmental transition in these cells. Notably, distinct regulation of SOX2 during early differentiation events was detected, highlighting the potential importance of this transcription factor for self-renewal of hES cells during differentiation.
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页数:12
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