Hepatic lipid overload triggers biliary epithelial cell activation via E2Fs.

Détails

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Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_8530865240EA
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Hepatic lipid overload triggers biliary epithelial cell activation via E2Fs.
Périodique
eLife
Auteur⸱e⸱s
Yildiz E., El Alam G., Perino A., Jalil A., Denechaud P.D., Huber K., Fajas L., Auwerx J., Sorrentino G., Schoonjans K.
ISSN
2050-084X (Electronic)
ISSN-L
2050-084X
Statut éditorial
Publié
Date de publication
06/03/2023
Peer-reviewed
Oui
Volume
12
Pages
e81926
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
During severe or chronic hepatic injury, biliary epithelial cells (BECs) undergo rapid activation into proliferating progenitors, a crucial step required to establish a regenerative process known as ductular reaction (DR). While DR is a hallmark of chronic liver diseases, including advanced stages of non-alcoholic fatty liver disease (NAFLD), the early events underlying BEC activation are largely unknown. Here, we demonstrate that BECs readily accumulate lipids during high-fat diet feeding in mice and upon fatty acid treatment in BEC-derived organoids. Lipid overload induces metabolic rewiring to support the conversion of adult cholangiocytes into reactive BECs. Mechanistically, we found that lipid overload activates the E2F transcription factors in BECs, which drive cell cycle progression while promoting glycolytic metabolism. These findings demonstrate that fat overload is sufficient to reprogram BECs into progenitor cells in the early stages of NAFLD and provide new insights into the mechanistic basis of this process, revealing unexpected connections between lipid metabolism, stemness, and regeneration.
Mots-clé
Animals, Mice, Non-alcoholic Fatty Liver Disease/metabolism, Liver/metabolism, Epithelial Cells/metabolism, Cell Division, Lipids, BEC activation, BEC-organoids, BECs, cell cycle, glycolysis, liver steatosis, mouse, regenerative medicine, stem cells
Pubmed
Web of science
Open Access
Oui
Création de la notice
16/03/2023 8:43
Dernière modification de la notice
08/08/2024 6:36
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