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Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD)
The prevalence of nonalcoholic fatty liver disease (NAFLD), recently also re-defined as metabolic dysfunction associated fatty liver disease (MAFLD), is rapidly increasing, affecting ~25% of the world population. MALFD/NAFLD represents a spectrum of liver pathologies including the more benign hepati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9266719/ https://www.ncbi.nlm.nih.gov/pubmed/35805998 http://dx.doi.org/10.3390/ijms23136996 |
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author | Subramanian, Pallavi Hampe, Jochen Tacke, Frank Chavakis, Triantafyllos |
author_facet | Subramanian, Pallavi Hampe, Jochen Tacke, Frank Chavakis, Triantafyllos |
author_sort | Subramanian, Pallavi |
collection | PubMed |
description | The prevalence of nonalcoholic fatty liver disease (NAFLD), recently also re-defined as metabolic dysfunction associated fatty liver disease (MAFLD), is rapidly increasing, affecting ~25% of the world population. MALFD/NAFLD represents a spectrum of liver pathologies including the more benign hepatic steatosis and the more advanced non-alcoholic steatohepatitis (NASH). NASH is associated with enhanced risk for liver fibrosis and progression to cirrhosis and hepatocellular carcinoma. Hepatic stellate cells (HSC) activation underlies NASH-related fibrosis. Here, we discuss the profibrogenic pathways, which lead to HSC activation and fibrogenesis, with a particular focus on the intercellular hepatocyte–HSC and macrophage–HSC crosstalk. |
format | Online Article Text |
id | pubmed-9266719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92667192022-07-09 Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) Subramanian, Pallavi Hampe, Jochen Tacke, Frank Chavakis, Triantafyllos Int J Mol Sci Review The prevalence of nonalcoholic fatty liver disease (NAFLD), recently also re-defined as metabolic dysfunction associated fatty liver disease (MAFLD), is rapidly increasing, affecting ~25% of the world population. MALFD/NAFLD represents a spectrum of liver pathologies including the more benign hepatic steatosis and the more advanced non-alcoholic steatohepatitis (NASH). NASH is associated with enhanced risk for liver fibrosis and progression to cirrhosis and hepatocellular carcinoma. Hepatic stellate cells (HSC) activation underlies NASH-related fibrosis. Here, we discuss the profibrogenic pathways, which lead to HSC activation and fibrogenesis, with a particular focus on the intercellular hepatocyte–HSC and macrophage–HSC crosstalk. MDPI 2022-06-23 /pmc/articles/PMC9266719/ /pubmed/35805998 http://dx.doi.org/10.3390/ijms23136996 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Subramanian, Pallavi Hampe, Jochen Tacke, Frank Chavakis, Triantafyllos Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) |
title | Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) |
title_full | Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) |
title_fullStr | Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) |
title_full_unstemmed | Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) |
title_short | Fibrogenic Pathways in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) |
title_sort | fibrogenic pathways in metabolic dysfunction associated fatty liver disease (mafld) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9266719/ https://www.ncbi.nlm.nih.gov/pubmed/35805998 http://dx.doi.org/10.3390/ijms23136996 |
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