Autophagy in chronic liver diseases: the two faces of Janus
- Others:
- Centre méditerranéen de médecine moléculaire (C3M) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Côte d'Azur (UniCA)
- Centre de recherche sur l'Inflammation (CRI (UMR_S_1149 / ERL_8252 / U1149)) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
- Univ Paris Est Créteil, INSERM, IMRB, F-94010 Créteil, France
- ANR-15-CE14-0016,HEPAMETOL,INTERACTION ENTRE ALCOOL ET L'OBÉSITÉ DANS LA SÉVÉRITÉ DES MALADIES DU FOIE GRAS.(2015)
- ANR-15-CE14-0031,HEPAMAG,La monoacylglycerol lipase: une nouvelle cible immunométabolique dans les maladies du foie(2015)
Description
Alcoholic liver disease (ALD) and nonalcoholic fatty liver disease (NAFLD) are the leading causes of cirrhosis and increase the risk of hepatocellular carcinoma and liver-related death. ALD and NAFLD share common pathogenic features extending from isolated steatosis to steatohepatitis and steatofibrosis, which can progress to cirrhosis and hepatocellular carcinoma. The pathophysiological mechanisms of the progression of NAFLD and ALD are complex and still unclear. Important links between the regulation of autophagy (macroautophagy and chaperone-mediated autophagy) and chronic liver diseases have been reported. Autophagy may protect against steatosis and progression to steatohepatitis by limiting hepatocyte injury and reducing M1 polarization, as well as promoting liver regeneration. Its role in fibrosis and hepatocarcinogenesis is more complex. It has pro- and antifibrogenic properties depending on the hepatic cell type concerned, and beneficial and deleterious effects on hepatocarcinogenesis at initiating and late phases, respectively. This review summarizes the latest advances on the role of autophagy in different stages of fatty liver disease progression and describes its divergent and cell-specific effects during chronic liver injury.
Abstract
International audience
Additional details
- URL
- https://hal.science/hal-04496721
- URN
- urn:oai:HAL:hal-04496721v1
- Origin repository
- UNICA