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Proteolysis dysfunction in the process of aging and age-related diseases
In this review, we discuss in detail the most relevant proteolytic systems that together with chaperones contribute to creating the proteostasis network that is kept in dynamic balance to maintain overall functionality of cellular proteomes. Data accumulated over decades demonstrate that the effecti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361021/ https://www.ncbi.nlm.nih.gov/pubmed/35958270 http://dx.doi.org/10.3389/fragi.2022.927630 |
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author | Frankowska, Natalia Lisowska, Katarzyna Witkowski, Jacek M. |
author_facet | Frankowska, Natalia Lisowska, Katarzyna Witkowski, Jacek M. |
author_sort | Frankowska, Natalia |
collection | PubMed |
description | In this review, we discuss in detail the most relevant proteolytic systems that together with chaperones contribute to creating the proteostasis network that is kept in dynamic balance to maintain overall functionality of cellular proteomes. Data accumulated over decades demonstrate that the effectiveness of elements of the proteostasis network declines with age. In this scenario, failure to degrade misfolded or faulty proteins increases the risk of protein aggregation, chronic inflammation, and the development of age-related diseases. This is especially important in the context of aging-related modification of functions of the immune system. |
format | Online Article Text |
id | pubmed-9361021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93610212022-08-10 Proteolysis dysfunction in the process of aging and age-related diseases Frankowska, Natalia Lisowska, Katarzyna Witkowski, Jacek M. Front Aging Aging In this review, we discuss in detail the most relevant proteolytic systems that together with chaperones contribute to creating the proteostasis network that is kept in dynamic balance to maintain overall functionality of cellular proteomes. Data accumulated over decades demonstrate that the effectiveness of elements of the proteostasis network declines with age. In this scenario, failure to degrade misfolded or faulty proteins increases the risk of protein aggregation, chronic inflammation, and the development of age-related diseases. This is especially important in the context of aging-related modification of functions of the immune system. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9361021/ /pubmed/35958270 http://dx.doi.org/10.3389/fragi.2022.927630 Text en Copyright © 2022 Frankowska, Lisowska and Witkowski. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Aging Frankowska, Natalia Lisowska, Katarzyna Witkowski, Jacek M. Proteolysis dysfunction in the process of aging and age-related diseases |
title | Proteolysis dysfunction in the process of aging and age-related diseases |
title_full | Proteolysis dysfunction in the process of aging and age-related diseases |
title_fullStr | Proteolysis dysfunction in the process of aging and age-related diseases |
title_full_unstemmed | Proteolysis dysfunction in the process of aging and age-related diseases |
title_short | Proteolysis dysfunction in the process of aging and age-related diseases |
title_sort | proteolysis dysfunction in the process of aging and age-related diseases |
topic | Aging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361021/ https://www.ncbi.nlm.nih.gov/pubmed/35958270 http://dx.doi.org/10.3389/fragi.2022.927630 |
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