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Control of liver cell fate decision by a gradient of TGFβ signaling modulated by Onecut transcription factors

机译:通过Onecut转录因子调节的TGFβ信号梯度控制肝细胞命运决定

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摘要

During liver development, hepatocytes and biliary cells differentiate from common progenitors called hepatoblasts. The factors that control hepatoblast fate decision are unknown. Here we report that a gradient of activin/TGFβ signaling controls hepatoblast differentiation. High activin/TGFβ signaling is required near the portal vein for differentiation of biliary cells. The Onecut transcription factors HNF-6 and OC-2 inhibit activin/TGFβ signaling in the parenchyma, and this allows normal hepatocyte differentiation. In the absence of Onecut factors, the shape of the activin/TGFβ gradient is perturbed and the hepatoblasts differentiate into hybrid cells that display characteristics of both hepatocytes and biliary cells. Thus, a gradient of activin/TGFβ signaling modulated by Onecut factors is required to segregate the hepatocytic and the biliary lineages.
机译:在肝脏发育过程中,肝细胞和胆道细胞与常见的祖细胞(称为成肝细胞)有所区别。控制成肝细胞命运决定的因素尚不清楚。在这里我们报告激活素/TGFβ信号的梯度控制成肝细胞分化。门静脉附近需要高水平的激活素/TGFβ信号来分化胆管细胞。 Onecut转录因子HNF-6和OC-2抑制实质中的激活素/TGFβ信号传导,这使正常肝细胞分化成为可能。在没有Onecut因子的情况下,激活素/TGFβ梯度的形状会受到干扰,并且成肝细胞分化为显示肝细胞和胆管细胞特征的杂种细胞。因此,需要通过Onecut因子调节的激活素/TGFβ信号传导梯度来分离肝细胞和胆道谱系。

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