IGF antagonizes the Wnt/β-Catenin pathway and promotes differentiation of extra-embryonic endoderm

Mouse F9 teratocarcinoma cells are an established model for the differentiation of extra-embryonic endoderm (ExEn). Primitive endoderm, parietal and visceral endoderm can be generated by stimulation of F9 cells with retinoic acid and dibutyryl cyclic adenosine monophosphate. Here we show that Wnt/β-...

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Bibliographic Details
Main Authors: Schlupf, Judith (Author) , Steinbeisser, Herbert (Author)
Format: Article (Journal)
Language:English
Published: 5 October 2014
In: Differentiation
Year: 2014, Volume: 87, Issue: 5, Pages: 209-219
ISSN:1432-0436
DOI:10.1016/j.diff.2014.07.003
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.diff.2014.07.003
Verlag, lizenzpflichtig, Volltext: http://www.sciencedirect.com/science/article/pii/S0301468114000498
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Author Notes:Judith Schlupf, Herbert Steinbeisser
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Summary:Mouse F9 teratocarcinoma cells are an established model for the differentiation of extra-embryonic endoderm (ExEn). Primitive endoderm, parietal and visceral endoderm can be generated by stimulation of F9 cells with retinoic acid and dibutyryl cyclic adenosine monophosphate. Here we show that Wnt/β-Catenin signaling is down-regulated during ExEn differentiation in F9 cells and that the inhibition of the Wnt pathway promotes differentiation of the three extra-embryonic endoderm lineages. Wnt inhibition is achieved through the IGF pathway, which is up-regulated during differentiation. IGF signaling antagonizes the Wnt pathway by stimulating transcription of axin2 and by stabilizing Axin1 protein. Both Axin1 and Axin2 are components of the β-Catenin destruction complex and act as intra-cellular inhibitors of the Wnt/β-Catenin pathway. The data presented reveal a mechanism which restricts pluripotency of undifferentiated cells and directs them toward extra-embryonic lineages.
Item Description:Gesehen am 13.08.2020
Physical Description:Online Resource
ISSN:1432-0436
DOI:10.1016/j.diff.2014.07.003