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Mitophagy in the Pathogenesis of Liver Diseases †

Autophagy is a catabolic process involving vacuolar sequestration of intracellular components and their targeting to lysosomes for degradation, thus supporting nutrient recycling and energy regeneration. Accumulating evidence indicates that in addition to being a bulk, nonselective degradation mecha...

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Autor principal: Ke, Po-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226805/
https://www.ncbi.nlm.nih.gov/pubmed/32235615
http://dx.doi.org/10.3390/cells9040831
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author Ke, Po-Yuan
author_facet Ke, Po-Yuan
author_sort Ke, Po-Yuan
collection PubMed
description Autophagy is a catabolic process involving vacuolar sequestration of intracellular components and their targeting to lysosomes for degradation, thus supporting nutrient recycling and energy regeneration. Accumulating evidence indicates that in addition to being a bulk, nonselective degradation mechanism, autophagy may selectively eliminate damaged mitochondria to promote mitochondrial turnover, a process termed “mitophagy”. Mitophagy sequesters dysfunctional mitochondria via ubiquitination and cargo receptor recognition and has emerged as an important event in the regulation of liver physiology. Recent studies have shown that mitophagy may participate in the pathogenesis of various liver diseases, such as liver injury, liver steatosis/fatty liver disease, hepatocellular carcinoma, viral hepatitis, and hepatic fibrosis. This review summarizes the current knowledge on the molecular regulations and functions of mitophagy in liver physiology and the roles of mitophagy in the development of liver-related diseases. Furthermore, the therapeutic implications of targeting hepatic mitophagy to design a new strategy to cure liver diseases are discussed.
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spelling pubmed-72268052020-05-18 Mitophagy in the Pathogenesis of Liver Diseases † Ke, Po-Yuan Cells Review Autophagy is a catabolic process involving vacuolar sequestration of intracellular components and their targeting to lysosomes for degradation, thus supporting nutrient recycling and energy regeneration. Accumulating evidence indicates that in addition to being a bulk, nonselective degradation mechanism, autophagy may selectively eliminate damaged mitochondria to promote mitochondrial turnover, a process termed “mitophagy”. Mitophagy sequesters dysfunctional mitochondria via ubiquitination and cargo receptor recognition and has emerged as an important event in the regulation of liver physiology. Recent studies have shown that mitophagy may participate in the pathogenesis of various liver diseases, such as liver injury, liver steatosis/fatty liver disease, hepatocellular carcinoma, viral hepatitis, and hepatic fibrosis. This review summarizes the current knowledge on the molecular regulations and functions of mitophagy in liver physiology and the roles of mitophagy in the development of liver-related diseases. Furthermore, the therapeutic implications of targeting hepatic mitophagy to design a new strategy to cure liver diseases are discussed. MDPI 2020-03-30 /pmc/articles/PMC7226805/ /pubmed/32235615 http://dx.doi.org/10.3390/cells9040831 Text en © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ke, Po-Yuan
Mitophagy in the Pathogenesis of Liver Diseases †
title Mitophagy in the Pathogenesis of Liver Diseases †
title_full Mitophagy in the Pathogenesis of Liver Diseases †
title_fullStr Mitophagy in the Pathogenesis of Liver Diseases †
title_full_unstemmed Mitophagy in the Pathogenesis of Liver Diseases †
title_short Mitophagy in the Pathogenesis of Liver Diseases †
title_sort mitophagy in the pathogenesis of liver diseases †
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226805/
https://www.ncbi.nlm.nih.gov/pubmed/32235615
http://dx.doi.org/10.3390/cells9040831
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