AbstractNotch signaling plays an acknowledged role in bile-duct development, but its involvement in cholangiocyte-fate determination remains incompletely understood. We investigated the effects of early Notch2 deletion in Notch2fl/fl/Alfp-Cretg/− (“Notch2-cKO”) and Notch2fl/fl/Alfp-Cre−/− (“control”) mice. Fetal and neonatal Notch2-cKO livers were devoid of cytokeratin19 (CK19)-, Dolichos-biflorus agglutinin (DBA)-, and SOX9-positive ductal structures, demonstrating absence of prenatal cholangiocyte differentiation. Despite extensive cholestatic hepatocyte necrosis and growth retardation, mortality was only ~15%. Unexpectedly, a slow process of secondary cholangiocyte differentiation and bile-duct formation was initiated around weaning that...
BACKGROUND AND OBJECTIVE: Persistent hepatic progenitor cells (HPC) activation resulting in ductular...
Background and objective: Persistent hepatic progenitor cells (HPC) activation resulting in ductular...
<p>(A) Immunofluorescence for Sox9, HNF4 and E-cadherin demonstrate that Lkb1 is required for the tr...
("control") mice. Fetal and neonatal Notch2-cKO livers were devoid of cytokeratin19 (CK19)-, Dolicho...
The Notch pathway is an evolutionary conserved, intercellular signaling pathway that plays an import...
SUMMARY Abnormal Notch signaling in humans results in Alagille syndrome, a pleiotropic disease chara...
In the mammalian liver, bile is transported to the intestine through an intricate network of bile du...
The mammalian biliary system, consisting of the intrahepatic and extrahepatic bile ducts, is respons...
The potential for intrahepatic bile duct (IHBD) regeneration in patients with bile duct insufficienc...
Notch signaling through the Notch2 receptor is essential for normal biliary tubulogenesis during liv...
COMMENTARY ON: Foxa1 and Foxa2 regulate bile duct development in mice. J Clin Invest 2009;119:1537–4...
BACKGROUND: Alagille syndrome is a developmental disorder caused predominantly by mutations in the J...
BACKGROUND & AIMS: Repair from biliary damages requires the biliary specification of hepatic progen...
<p>A–D. HNF1β expression in <i>Notch2-cko</i> mice at P7 and P0. E,F. HNF6 expression in <i>Jag1<sup...
International audienceBACKGROUND:LKB1 is an evolutionary conserved kinase implicated in a wide range...
BACKGROUND AND OBJECTIVE: Persistent hepatic progenitor cells (HPC) activation resulting in ductular...
Background and objective: Persistent hepatic progenitor cells (HPC) activation resulting in ductular...
<p>(A) Immunofluorescence for Sox9, HNF4 and E-cadherin demonstrate that Lkb1 is required for the tr...
("control") mice. Fetal and neonatal Notch2-cKO livers were devoid of cytokeratin19 (CK19)-, Dolicho...
The Notch pathway is an evolutionary conserved, intercellular signaling pathway that plays an import...
SUMMARY Abnormal Notch signaling in humans results in Alagille syndrome, a pleiotropic disease chara...
In the mammalian liver, bile is transported to the intestine through an intricate network of bile du...
The mammalian biliary system, consisting of the intrahepatic and extrahepatic bile ducts, is respons...
The potential for intrahepatic bile duct (IHBD) regeneration in patients with bile duct insufficienc...
Notch signaling through the Notch2 receptor is essential for normal biliary tubulogenesis during liv...
COMMENTARY ON: Foxa1 and Foxa2 regulate bile duct development in mice. J Clin Invest 2009;119:1537–4...
BACKGROUND: Alagille syndrome is a developmental disorder caused predominantly by mutations in the J...
BACKGROUND & AIMS: Repair from biliary damages requires the biliary specification of hepatic progen...
<p>A–D. HNF1β expression in <i>Notch2-cko</i> mice at P7 and P0. E,F. HNF6 expression in <i>Jag1<sup...
International audienceBACKGROUND:LKB1 is an evolutionary conserved kinase implicated in a wide range...
BACKGROUND AND OBJECTIVE: Persistent hepatic progenitor cells (HPC) activation resulting in ductular...
Background and objective: Persistent hepatic progenitor cells (HPC) activation resulting in ductular...
<p>(A) Immunofluorescence for Sox9, HNF4 and E-cadherin demonstrate that Lkb1 is required for the tr...