| Literature DB >> 31914606 |
Marta Cruces-Sande1,2,3, Alba C Arcones1,2,3, Rocío Vila-Bedmar4, Almudena Val-Blasco1,2,3, Kfir Sharabi5,6, Daniel Díaz-Rodríguez1, Pere Puigserver5,6, Federico Mayor1,2,3, Cristina Murga1,2,3.
Abstract
The liver plays a key role during fasting to maintain energy homeostasis and euglycemia via metabolic processes mainly orchestrated by the insulin/glucagon ratio. We report here that fasting or calorie restriction protocols in C57BL6 mice promote a marked decrease in the hepatic protein levels of G protein-coupled receptor kinase 2 (GRK2), an important negative modulator of both G protein-coupled receptors (GPCRs) and insulin signaling. Such downregulation of GRK2 levels is liver-specific and can be rapidly reversed by refeeding. We find that autophagy, and not the proteasome, represents the main mechanism implicated in fasting-induced GRK2 degradation in the liver in vivo. Reducing GRK2 levels in murine primary hepatocytes facilitates glucagon-induced glucose production and enhances the expression of the key gluconeogenic enzyme Pck1. Conversely, preventing full downregulation of hepatic GRK2 during fasting using adenovirus-driven overexpression of this kinase in the liver leads to glycogen accumulation, decreased glycemia, and hampered glucagon-induced gluconeogenesis, thus preventing a proper and complete adaptation to nutrient deprivation. Overall, our data indicate that physiological fasting-induced downregulation of GRK2 in the liver is key for allowing complete glucagon-mediated responses and efficient metabolic adaptation to fasting in vivo.Entities:
Keywords: GPCR; GRK2; autophagy; calorie restriction; fasting; glucagon signaling; gluconeogenesis; intermittent fasting
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Year: 2019 PMID: 31914606 PMCID: PMC7184883 DOI: 10.1096/fj.201901444R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191