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Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells
The ageing of the global population brings about unprecedented challenges. Chronic age‐related diseases in an increasing number of people represent an enormous burden for health and social care. The immune system deteriorates during ageing and contributes to many of these age‐associated diseases due...
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/PMC7884036/ https://www.ncbi.nlm.nih.gov/pubmed/33524238 http://dx.doi.org/10.1111/acel.13316 |
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author | Zhou, Dingxi Borsa, Mariana Simon, Anna Katharina |
author_facet | Zhou, Dingxi Borsa, Mariana Simon, Anna Katharina |
author_sort | Zhou, Dingxi |
collection | PubMed |
description | The ageing of the global population brings about unprecedented challenges. Chronic age‐related diseases in an increasing number of people represent an enormous burden for health and social care. The immune system deteriorates during ageing and contributes to many of these age‐associated diseases due to its pivotal role in pathogen clearance, tissue homeostasis and maintenance. Moreover, in order to develop treatments for COVID‐19, we urgently need to acquire more knowledge about the aged immune system, as older adults are disproportionally and more severely affected. Changes with age lead to impaired responses to infections, malignancies and vaccination, and are accompanied by chronic, low‐degree inflammation, which together is termed immunosenescence. However, the molecular and cellular mechanisms that underlie immunosenescence, termed immune cell senescence, are mostly unknown. Cellular senescence, characterised by an irreversible cell cycle arrest, is thought to be the cause of tissue and organismal ageing. Thus, better understanding of cellular senescence in immune populations at single‐cell level may provide us with insight into how immune cell senescence develops over the life time of an individual. In this review, we will briefly introduce the phenotypic characterisation of aged innate and adaptive immune cells, which also contributes to overall immunosenescence, including subsets and function. Next, we will focus on the different hallmarks of cellular senescence and cellular ageing, and the detection techniques most suitable for immune cells. Applying these techniques will deepen our understanding of immune cell senescence and to discover potential druggable pathways, which can be modulated to reverse immune ageing. |
format | Online Article Text |
id | pubmed-7884036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78840362021-02-19 Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells Zhou, Dingxi Borsa, Mariana Simon, Anna Katharina Aging Cell Reviews The ageing of the global population brings about unprecedented challenges. Chronic age‐related diseases in an increasing number of people represent an enormous burden for health and social care. The immune system deteriorates during ageing and contributes to many of these age‐associated diseases due to its pivotal role in pathogen clearance, tissue homeostasis and maintenance. Moreover, in order to develop treatments for COVID‐19, we urgently need to acquire more knowledge about the aged immune system, as older adults are disproportionally and more severely affected. Changes with age lead to impaired responses to infections, malignancies and vaccination, and are accompanied by chronic, low‐degree inflammation, which together is termed immunosenescence. However, the molecular and cellular mechanisms that underlie immunosenescence, termed immune cell senescence, are mostly unknown. Cellular senescence, characterised by an irreversible cell cycle arrest, is thought to be the cause of tissue and organismal ageing. Thus, better understanding of cellular senescence in immune populations at single‐cell level may provide us with insight into how immune cell senescence develops over the life time of an individual. In this review, we will briefly introduce the phenotypic characterisation of aged innate and adaptive immune cells, which also contributes to overall immunosenescence, including subsets and function. Next, we will focus on the different hallmarks of cellular senescence and cellular ageing, and the detection techniques most suitable for immune cells. Applying these techniques will deepen our understanding of immune cell senescence and to discover potential druggable pathways, which can be modulated to reverse immune ageing. John Wiley and Sons Inc. 2021-02-01 2021-02 /pmc/articles/PMC7884036/ /pubmed/33524238 http://dx.doi.org/10.1111/acel.13316 Text en © 2021 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Zhou, Dingxi Borsa, Mariana Simon, Anna Katharina Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells |
title | Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells |
title_full | Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells |
title_fullStr | Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells |
title_full_unstemmed | Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells |
title_short | Hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells |
title_sort | hallmarks and detection techniques of cellular senescence and cellular ageing in immune cells |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884036/ https://www.ncbi.nlm.nih.gov/pubmed/33524238 http://dx.doi.org/10.1111/acel.13316 |
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