Sox17 Regulates Organ Lineage Segregation of Ventral Foregut Progenitor Cells

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The ventral pancreas, biliary system, and liver arise from the posterior ventral foregut, but the cell-intrinsic pathway by which these organ lineages are separated is not known. Here we show that the extra-hepatobiliary system shares a common origin with the ventral pancreas and not the liver, as previously thought. These pancreatobiliary progenitor cells coexpress the transcription factors PDX1 and SOX17 at E8.5 and their segregation into a PDX1 + ventral pancreas and a SOX17 + biliary primordium is Sox17-dependent. Deletion of Sox17 at E8.5 results in the loss of biliary structures and ectopic pancreatic tissue in the liver bud and common duct, while Sox17 overexpression suppresses pancreas development and promotes ectopic biliary-like tissue throughout the PDX1 + domain. Restricting SOX17 + biliary progenitor cells to the ventral region of the gut requires the notch effector Hes 1. Our results highlight the role of Sox17 and Hes1 in patterning and morphogenetic segregation of ventral foregut lineages.
Publisher
CELL PRESS
Issue Date
2009-07
Language
English
Article Type
Article
Keywords

AUTOSOMAL RECESSIVE SYNDROME; PANCREATIC ENDOCRINE-CELLS; NEONATAL DIABETES-MELLITUS; GALL-BLADDER; BILE-DUCTS; HYPOPLASTIC PANCREAS; EXOCRINE PANCREAS; ANNULAR PANCREAS; BETA-CATENIN; GUT ENDODERM

Citation

DEVELOPMENTAL CELL, v.17, no.1, pp.62 - 74

ISSN
1534-5807
DOI
10.1016/j.devcel.2009.05.012
URI
http://hdl.handle.net/10203/13447
Appears in Collection
MSE-Journal Papers(저널논문)
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