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Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments
The aging process is represented by the time‐dependent decay in physiologic functions of living beings. Major interest has been focused in recent years on the determinants of this progressive condition due to its correlative relationship with the onset of diseases. Several hallmark features have bee...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279468/ https://www.ncbi.nlm.nih.gov/pubmed/34278165 http://dx.doi.org/10.1002/hep4.1725 |
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author | Baiocchi, Leonardo Glaser, Shannon Francis, Heather Kennedy, Lindsey Felli, Eric Alpini, Gianfranco Gracia‐Sancho, Jordi |
author_facet | Baiocchi, Leonardo Glaser, Shannon Francis, Heather Kennedy, Lindsey Felli, Eric Alpini, Gianfranco Gracia‐Sancho, Jordi |
author_sort | Baiocchi, Leonardo |
collection | PubMed |
description | The aging process is represented by the time‐dependent decay in physiologic functions of living beings. Major interest has been focused in recent years on the determinants of this progressive condition due to its correlative relationship with the onset of diseases. Several hallmark features have been observed in aging, such as genetic alterations, mitochondrial impairment, and telomere shortening. At the cellular level, a senescent phenotype has been identified in response to aging that is characterized by a flat appearance, proliferative arrest, and production of specific molecules. The net effect of these cells in the course of diseases is an argument of debate. In fact, while the onset of a senescent phenotype may prevent tumor spreading, these cells appear to support pathological processes in some conditions. Several studies are now focused on clarifying the specific molecular pathways of aging/senescence in different cells, tissues, or organs. Biliary and vascular components, within the liver, have emerged as important determinants of some form of liver disease. In this review we summarize the most recent achievements on aging/senescence, focusing on the biliary and vascular liver system. Conclusion: Several findings, in both preclinical animal models and on human liver specimens, converge in supporting the presence of specific aging hallmarks in the diseases involving these hepatic compartments. |
format | Online Article Text |
id | pubmed-8279468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82794682021-07-15 Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments Baiocchi, Leonardo Glaser, Shannon Francis, Heather Kennedy, Lindsey Felli, Eric Alpini, Gianfranco Gracia‐Sancho, Jordi Hepatol Commun Reviews The aging process is represented by the time‐dependent decay in physiologic functions of living beings. Major interest has been focused in recent years on the determinants of this progressive condition due to its correlative relationship with the onset of diseases. Several hallmark features have been observed in aging, such as genetic alterations, mitochondrial impairment, and telomere shortening. At the cellular level, a senescent phenotype has been identified in response to aging that is characterized by a flat appearance, proliferative arrest, and production of specific molecules. The net effect of these cells in the course of diseases is an argument of debate. In fact, while the onset of a senescent phenotype may prevent tumor spreading, these cells appear to support pathological processes in some conditions. Several studies are now focused on clarifying the specific molecular pathways of aging/senescence in different cells, tissues, or organs. Biliary and vascular components, within the liver, have emerged as important determinants of some form of liver disease. In this review we summarize the most recent achievements on aging/senescence, focusing on the biliary and vascular liver system. Conclusion: Several findings, in both preclinical animal models and on human liver specimens, converge in supporting the presence of specific aging hallmarks in the diseases involving these hepatic compartments. John Wiley and Sons Inc. 2021-04-10 /pmc/articles/PMC8279468/ /pubmed/34278165 http://dx.doi.org/10.1002/hep4.1725 Text en © 2021 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of the American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Reviews Baiocchi, Leonardo Glaser, Shannon Francis, Heather Kennedy, Lindsey Felli, Eric Alpini, Gianfranco Gracia‐Sancho, Jordi Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments |
title | Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments |
title_full | Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments |
title_fullStr | Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments |
title_full_unstemmed | Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments |
title_short | Impact of Aging on Liver Cells and Liver Disease: Focus on the Biliary and Vascular Compartments |
title_sort | impact of aging on liver cells and liver disease: focus on the biliary and vascular compartments |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279468/ https://www.ncbi.nlm.nih.gov/pubmed/34278165 http://dx.doi.org/10.1002/hep4.1725 |
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