E2F1 promotes hepatic gluconeogenesis and contributes to hyperglycemia during diabetes.

Détails

Ressource 1Télécharger: 1-s2.0-S2212877818300577-main.pdf (759.72 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_ED95377F8A23
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
E2F1 promotes hepatic gluconeogenesis and contributes to hyperglycemia during diabetes.
Périodique
Molecular metabolism
Auteur(s)
Giralt A., Denechaud P.D., Lopez-Mejia I.C., Delacuisine B., Blanchet E., Bonner C., Pattou F., Annicotte J.S., Fajas L.
ISSN
2212-8778 (Electronic)
ISSN-L
2212-8778
Statut éditorial
Publié
Date de publication
05/2018
Peer-reviewed
Oui
Volume
11
Pages
104-112
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Aberrant hepatic glucose production contributes to the development of hyperglycemia and is a hallmark of type 2 diabetes. In a recent study, we showed that the transcription factor E2F1, a component of the cell cycle machinery, contributes to hepatic steatosis through the transcriptional regulation of key lipogenic enzymes. Here, we investigate if E2F1 contributes to hyperglycemia by regulating hepatic gluconeogenesis.
We use different genetic models to investigate if E2F1 regulates gluconeogenesis in primary hepatocytes and in vivo. We study the impact of depleting E2F1 or inhibiting E2F1 activity in diabetic mouse models to evaluate if this transcription factor contributes to hyperglycemia during insulin resistance. We analyze E2F1 mRNA levels in the livers of human diabetic patients to assess the relevance of E2F1 in human pathophysiology.
Lack of E2F1 impaired gluconeogenesis in primary hepatocytes. Conversely, E2F1 overexpression increased glucose production in hepatocytes and in mice. Several genetic models showed that the canonical CDK4-RB1-E2F1 pathway is directly involved in this regulation. E2F1 mRNA levels were increased in the livers from human diabetic patients and correlated with the expression of the gluconeogenic enzyme Pck1. Genetic invalidation or pharmacological inhibition of E2F1 improved glucose homeostasis in diabetic mouse models.
Our study unveils that the transcription factor E2F1 contributes to mammalian glucose homeostasis by directly controlling hepatic gluconeogenesis. Together with our previous finding that E2F1 promotes hepatic steatosis, the data presented here show that E2F1 contributes to both hyperlipidemia and hyperglycemia in diabetes, suggesting that specifically targeting E2F1 in the liver could be an interesting strategy for therapies against type 2 diabetes.
Mots-clé
Animals, Cells, Cultured, Diabetes Mellitus, Type 2/metabolism, E2F1 Transcription Factor/genetics, E2F1 Transcription Factor/metabolism, Gluconeogenesis, Hep G2 Cells, Humans, Hyperglycemia/metabolism, Liver/metabolism, Mice, Mice, Inbred C57BL, Signal Transduction, Cell cycle regulators, Diabetes, E2F1, Hyperglycemia, Liver metabolism
Pubmed
Web of science
Open Access
Oui
Création de la notice
15/03/2018 19:38
Dernière modification de la notice
20/08/2019 17:15
Données d'usage