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NKX2-1 Activation by SMAD2 Signaling After Definitive Endoderm Differentiation in Human Embryonic Stem Cell

机译:在人类胚胎干细胞确定性内胚层分化后通过SMAD2信号激活NKX2-1。

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摘要

Expression of NKX2-1 is required to specify definitive endoderm to respiratory endoderm. However, the transcriptional regulation of NKX2-1 is not fully understood. Here we demonstrate that aside from specifying undifferentiated human embryonic stem cell (hESC) to definitive endoderm, high concentrations of Activin-A are also necessary and sufficient to induce hESC-derived definitive endodermal progeny to a FOXA2/NKX2-1/GATA6/PAX9 positive respiratory epithelial fate. Activin-A directly mediates the induction of NKX2-1 by interacting with ALK4, leading to phosphorylation of SMAD2, which binds directly to the NKX2-1 promoter and activates its expression. Activin-A can be replaced by GDF11 but not transforming growth factor β1. Addition of Wnt3a, SHH, FGF2, or BMP4 failed to induce NKX2-1. These results suggest that direct binding of Activin-A–responsive SMAD2 to the NKX2-1 promoter plays essential role during respiratory endoderm specification.
机译:需要表达NKX2-1才能确定呼吸道内胚层的定形内胚层。但是,NKX2-1的转录调控尚未完全了解。在这里,我们证明,除了将未分化的人类胚胎干细胞(hESC)指定为定形内胚层之外,高浓度的Activin-A也是必要且足以诱导hESC衍生的定形内胚层后代为FOXA2 / NKX2-1 / GATA6 / PAX9阳性呼吸道上皮的命运。激活素A通过与ALK4相互作用直接介导NKX2-1的诱导,导致SMAD2磷酸化,SMAD2直接与NKX2-1启动子结合并激活其表达。活化素A可以被GDF11取代,但不能转化生长因子β1。 Wnt3a,SHH,FGF2或BMP4的添加未能诱导NKX2-1。这些结果表明,激活素A应答的SMAD2与NKX2-1启动子的直接结合在呼吸内胚层规范过程中起着至关重要的作用。

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