Cell heterogeneity and fate bistability drive tissue patterning during intestinal regeneration
- Datum
- 11.02.2025
- Zeit
- 10:00 - 11:00
- Sprecher
- Cornelia Schwayer
- Zugehörigkeit
- ETH Zürich | Dept. for Biosystems Science and Engineering (D-BSSE) & Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland
- Sprache
- en
- Hauptthema
- Biologie
- Host
- Meritxell Huch
- Beschreibung
- Tissue regeneration relies on the ability of cells to undergo de novopatterning. While tissue patterning has been viewed as the transition from initially identical un-patterned cells to an arrangement of different cell types, recent evidence suggests that initial heterogeneities between cells modulate tissue-scale pattern formation. Yet, how such heterogeneities arise and, thereafter, regulate cell type emergence in a population of cells is poorly understood. Using in vivo and in vitro mouseregenerative systems, we identify a critical tissue density that is required to induce heterogeneous inactivation of the mechanosensor YAP1. Experimental and biophysical approaches demonstrate that YAP1 cell-to-cell heterogeneity pre-patterns the first cell fate decision, via both chromatin remodelling and a supracellular feedback between FOXA1 and Delta-Notch signalling. This feedback motif induces cell fate bistability endowing memory to the system and the maintenance of patterns during homeostasis. These findings reveal a generalisable framework in which transient cell-to-cell heterogeneity, regulated by tissue-scale properties, serves as a critical control parameter for the emergence of cell fate and stable patterning during regeneration.
Letztmalig verändert: 11.02.2025, 07:35:30
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Max Planck Institute of Molecular Cell Biology and GeneticsPfotenhauerstraße10801307Dresden
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- +49 351 210-0
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- +49 351 210-2000
- MPI-CBG
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- http://www.mpi-cbg.de
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