Inhibition of β-catenin-TCF1 interaction delays differentiation of mouse embryonic stem cells

J Cell Biol. 2015 Oct 12;211(1):39-51. doi: 10.1083/jcb.201503017.

Abstract

The ability of mouse embryonic stem cells (mESCs) to self-renew or differentiate into various cell lineages is regulated by signaling pathways and a core pluripotency transcriptional network (PTN) comprising Nanog, Oct4, and Sox2. The Wnt/β-catenin pathway promotes pluripotency by alleviating T cell factor TCF3-mediated repression of the PTN. However, it has remained unclear how β-catenin's function as a transcriptional activator with TCF1 influences mESC fate. Here, we show that TCF1-mediated transcription is up-regulated in differentiating mESCs and that chemical inhibition of β-catenin/TCF1 interaction improves long-term self-renewal and enhances functional pluripotency. Genetic loss of TCF1 inhibited differentiation by delaying exit from pluripotency and conferred a transcriptional profile strikingly reminiscent of self-renewing mESCs with high Nanog expression. Together, our data suggest that β-catenin's function in regulating mESCs is highly context specific and that its interaction with TCF1 promotes differentiation, further highlighting the need for understanding how its individual protein-protein interactions drive stem cell fate.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation*
  • Cell Self Renewal
  • Cells, Cultured
  • Hepatocyte Nuclear Factor 1-alpha / antagonists & inhibitors
  • Hepatocyte Nuclear Factor 1-alpha / metabolism*
  • Mice
  • Mouse Embryonic Stem Cells / physiology*
  • Oxazoles / pharmacology
  • Transcription, Genetic
  • beta Catenin / antagonists & inhibitors
  • beta Catenin / metabolism*

Substances

  • CTNNB1 protein, mouse
  • Hepatocyte Nuclear Factor 1-alpha
  • Hnf1a protein, mouse
  • Oxazoles
  • beta Catenin
  • iCRT3 compound