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

2005; Cold Spring Harbor Laboratory Press; Volume: 19; Issue: 16 Linguagem: Inglês

10.1101/gad.340305

1549-5477

Frédéric Clotman, Patrick Jacquemin, Nicolas Plumb–Rudewiez, Christophe E. Pierreux, Patrick Van Deŕ Smissen, Harry C. Dietz, Pierre J. Courtoy, Guy Rousseau, Frédéric P. Lemaigre,

Pancreatic and Hepatic Oncology Research

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/TGFbeta signaling controls hepatoblast differentiation. High activin/TGFbeta signaling is required near the portal vein for differentiation of biliary cells. The Onecut transcription factors HNF-6 and OC-2 inhibit activin/TGFbeta signaling in the parenchyma, and this allows normal hepatocyte differentiation. In the absence of Onecut factors, the shape of the activin/TGFbeta gradient is perturbed and the hepatoblasts differentiate into hybrid cells that display characteristics of both hepatocytes and biliary cells. Thus, a gradient of activin/TGFbeta signaling modulated by Onecut factors is required to segregate the hepatocytic and the biliary lineages.