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Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells
Understanding the aging process and ways to manipulate it is of major importance for biology and medicine. Among the many aging theories advanced over the years, the concept most consistent with experimental evidence posits the buildup of numerous forms of molecular damage as a foundation of the agi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351832/ https://www.ncbi.nlm.nih.gov/pubmed/30346102 http://dx.doi.org/10.1111/acel.12841 |
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author | Ogrodnik, Mikolaj Salmonowicz, Hanna Gladyshev, Vadim N. |
author_facet | Ogrodnik, Mikolaj Salmonowicz, Hanna Gladyshev, Vadim N. |
author_sort | Ogrodnik, Mikolaj |
collection | PubMed |
description | Understanding the aging process and ways to manipulate it is of major importance for biology and medicine. Among the many aging theories advanced over the years, the concept most consistent with experimental evidence posits the buildup of numerous forms of molecular damage as a foundation of the aging process. Here, we discuss that this concept integrates well with recent findings on cellular senescence, offering a novel view on the role of senescence in aging and age‐related disease. Cellular senescence has a well‐established role in cellular aging, but its impact on the rate of organismal aging is less defined. One of the most prominent features of cellular senescence is its association with macromolecular damage. The relationship between cell senescence and damage concerns both damage as a molecular signal of senescence induction and accelerated accumulation of damage in senescent cells. We describe the origin, regulatory mechanisms, and relevance of various damage forms in senescent cells. This view on senescent cells as carriers and inducers of damage puts new light on senescence, considering it as a significant contributor to the rise in organismal damage. Applying these ideas, we critically examine current evidence for a role of cellular senescence in aging and age‐related diseases. We also discuss the differential impact of longevity interventions on senescence burden and other types of age‐related damage. Finally, we propose a model on the role of aging‐related damage accumulation and the rate of aging observed upon senescent cell clearance. |
format | Online Article Text |
id | pubmed-6351832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63518322019-02-07 Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells Ogrodnik, Mikolaj Salmonowicz, Hanna Gladyshev, Vadim N. Aging Cell Reviews Understanding the aging process and ways to manipulate it is of major importance for biology and medicine. Among the many aging theories advanced over the years, the concept most consistent with experimental evidence posits the buildup of numerous forms of molecular damage as a foundation of the aging process. Here, we discuss that this concept integrates well with recent findings on cellular senescence, offering a novel view on the role of senescence in aging and age‐related disease. Cellular senescence has a well‐established role in cellular aging, but its impact on the rate of organismal aging is less defined. One of the most prominent features of cellular senescence is its association with macromolecular damage. The relationship between cell senescence and damage concerns both damage as a molecular signal of senescence induction and accelerated accumulation of damage in senescent cells. We describe the origin, regulatory mechanisms, and relevance of various damage forms in senescent cells. This view on senescent cells as carriers and inducers of damage puts new light on senescence, considering it as a significant contributor to the rise in organismal damage. Applying these ideas, we critically examine current evidence for a role of cellular senescence in aging and age‐related diseases. We also discuss the differential impact of longevity interventions on senescence burden and other types of age‐related damage. Finally, we propose a model on the role of aging‐related damage accumulation and the rate of aging observed upon senescent cell clearance. John Wiley and Sons Inc. 2018-10-22 2019-02 /pmc/articles/PMC6351832/ /pubmed/30346102 http://dx.doi.org/10.1111/acel.12841 Text en © 2018 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 Ogrodnik, Mikolaj Salmonowicz, Hanna Gladyshev, Vadim N. Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells |
title | Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells |
title_full | Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells |
title_fullStr | Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells |
title_full_unstemmed | Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells |
title_short | Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells |
title_sort | integrating cellular senescence with the concept of damage accumulation in aging: relevance for clearance of senescent cells |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351832/ https://www.ncbi.nlm.nih.gov/pubmed/30346102 http://dx.doi.org/10.1111/acel.12841 |
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