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Dev Cell ; 49(1): 31-47.e9, 2019 04 08.
Article in English | MEDLINE | ID: mdl-30853440

ABSTRACT

The mechanism of how organ shape emerges and specifies cell fate is not understood. Pancreatic duct and endocrine lineages arise in a spatially distinct domain from the acinar lineage. Whether these lineages are pre-determined or settle once these niches have been established remains unknown. Here, we reconcile these two apparently opposing models, demonstrating that pancreatic progenitors re-localize to establish the niche that will determine their ultimate fate. We identify a p120ctn-regulated mechanism for coordination of organ architecture and cellular fate mediated by differential E-cadherin based cell sorting. Reduced p120ctn expression is necessary and sufficient to re-localize a subset of progenitors to the peripheral tip domain, where they acquire an acinar fate. The same mechanism is used re-iteratively during endocrine specification, where it balances the choice between the alpha and beta cell fates. In conclusion, organ patterning is regulated by p120ctn-mediated cellular positioning, which precedes and determines pancreatic progenitor fate.


Subject(s)
Body Patterning/genetics , Catenins/genetics , Pancreas/growth & development , Pancreatic Ducts/growth & development , Animals , Cadherins/genetics , Cell Differentiation/genetics , Cell Lineage/genetics , Cell Movement/genetics , Embryonic Development/genetics , Flow Cytometry , Gene Expression Regulation, Developmental , Humans , Islets of Langerhans/growth & development , Islets of Langerhans/metabolism , Mice , Pancreas/metabolism , Receptors, Notch/genetics , Signal Transduction/genetics , Stem Cells/metabolism , Delta Catenin
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