4.8 Review

Autophagy in hepatic adaptation to stress

期刊

JOURNAL OF HEPATOLOGY
卷 72, 期 1, 页码 183-196

出版社

ELSEVIER
DOI: 10.1016/j.jhep.2019.08.026

关键词

Aggrephagy; Chaperone-mediated autophagy; Lipid droplets; Lipophagy; Mitophagy; Unfolded protein response

资金

  1. FONDECYT [3180427, 1140549, 1180186]
  2. Breakthrough Level 2 grant from the US DoD, Breast Cancer Research Program (BCRP) [BC180476P1]
  3. Dept. of Radiation Oncology at Weill Cornell Medicine (New York, US)
  4. Lytix (Oslo, Norway)
  5. Phosplatin (New York, US)
  6. FONDAP program [15150012]
  7. Millennium Institute [P09-015-F]
  8. European Commission RD MSCA-RISE [734749]
  9. Michael J Fox Foundation for Parkinson's Research - Target Validation grant [9277]
  10. FONDEF [ID16I10223, D11E1007]
  11. US Office of Naval Research -Global (ONR-G) [N62909-16-1-2003]
  12. U.S. Air Force Office of Scientific Research [FA9550-16-1-0384]
  13. ALSRP Therapeutic Idea Award [AL150111]
  14. Muscular Dystrophy Association [382453]
  15. CONICYT Brazil [441921/2016-7]
  16. Ligue contre le Cancer (equipe labellisee)
  17. Agence National de la Recherche (ANR) - Projets blancs
  18. ANR under the frame of E-Rare-2, the ERA-Net for Research on Rare Diseases
  19. Association pour la recherche sur le cancer (ARC)
  20. Canceropole Ilede-France
  21. Chancelerie des universites de Paris (Legs Poix), Fondation pour la Recherche Medicale (FRM)
  22. European Research Area Network on Cardiovascular Diseases (ERACVD, MINOTAUR)
  23. Gustave Roussy Odyssea, the European Union Horizon 2020 Project Oncobiome
  24. Fondation Carrefour
  25. High-end Foreign Expert Program in China, Institut National du Cancer (INCa) [GDW20171100085, GDW20181100051]
  26. Inserm (HTE)
  27. Inserm Transfert, Institut Universitaire de France
  28. LeDucq Foundation
  29. LabEx Immuno-Oncology
  30. RHU Torino Lumiere
  31. Seerave Foundation
  32. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  33. SIRIC Cancer Research and Personalized Medicine (CARPEM)

向作者/读者索取更多资源

Autophagy is an evolutionarily ancient process whereby eukaryotic cells eliminate disposable or potentially dangerous cytoplasmic material, to support bioenergetic metabolism and adapt to stress. Accumulating evidence indicates that autophagy operates as a critical quality control mechanism for the maintenance of hepatic homeostasis in both parenchymal (hepatocytes) and non-parenchymal (stellate cells, sinusoidal endothelial cells, Kupffer cells) compartments. In line with this notion, insufficient autophagy has been aetiologically involved in the pathogenesis of multiple liver disorders, including alpha-1-antitrypsin deficiency, Wilson disease, non-alcoholic steatohepatitis, liver fibrosis and hepatocellular carcinoma. Here, we critically discuss the importance of functional autophagy for hepatic physiology, as well as the mechanisms whereby defects in autophagy cause liver disease. (C) 2019 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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