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Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality

Aging is a complex biological process involving multiple interacting mechanisms and is being increasingly linked to environmental exposures such as wildfire smoke. In this review, we detail the hallmarks of aging, emphasizing the role of telomere attrition, cellular senescence, epigenetic alteration...

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Autores principales: Scieszka, David, Bolt, Alicia M., McCormick, Mark A., Brigman, Jonathan L., Campen, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600394/
https://www.ncbi.nlm.nih.gov/pubmed/37900096
http://dx.doi.org/10.3389/ftox.2023.1267667
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author Scieszka, David
Bolt, Alicia M.
McCormick, Mark A.
Brigman, Jonathan L.
Campen, Matthew J.
author_facet Scieszka, David
Bolt, Alicia M.
McCormick, Mark A.
Brigman, Jonathan L.
Campen, Matthew J.
author_sort Scieszka, David
collection PubMed
description Aging is a complex biological process involving multiple interacting mechanisms and is being increasingly linked to environmental exposures such as wildfire smoke. In this review, we detail the hallmarks of aging, emphasizing the role of telomere attrition, cellular senescence, epigenetic alterations, proteostasis, genomic instability, and mitochondrial dysfunction, while also exploring integrative hallmarks - altered intercellular communication and stem cell exhaustion. Within each hallmark of aging, our review explores how environmental disasters like wildfires, and their resultant inhaled toxicants, interact with these aging mechanisms. The intersection between aging and environmental exposures, especially high-concentration insults from wildfires, remains under-studied. Preliminary evidence, from our group and others, suggests that inhaled wildfire smoke can accelerate markers of neurological aging and reduce learning capabilities. This is likely mediated by the augmentation of circulatory factors that compromise vascular and blood-brain barrier integrity, induce chronic neuroinflammation, and promote age-associated proteinopathy-related outcomes. Moreover, wildfire smoke may induce a reduced metabolic, senescent cellular phenotype. Future interventions could potentially leverage combined anti-inflammatory and NAD + boosting compounds to counter these effects. This review underscores the critical need to study the intricate interplay between environmental factors and the biological mechanisms of aging to pave the way for effective interventions.
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spelling pubmed-106003942023-10-27 Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality Scieszka, David Bolt, Alicia M. McCormick, Mark A. Brigman, Jonathan L. Campen, Matthew J. Front Toxicol Toxicology Aging is a complex biological process involving multiple interacting mechanisms and is being increasingly linked to environmental exposures such as wildfire smoke. In this review, we detail the hallmarks of aging, emphasizing the role of telomere attrition, cellular senescence, epigenetic alterations, proteostasis, genomic instability, and mitochondrial dysfunction, while also exploring integrative hallmarks - altered intercellular communication and stem cell exhaustion. Within each hallmark of aging, our review explores how environmental disasters like wildfires, and their resultant inhaled toxicants, interact with these aging mechanisms. The intersection between aging and environmental exposures, especially high-concentration insults from wildfires, remains under-studied. Preliminary evidence, from our group and others, suggests that inhaled wildfire smoke can accelerate markers of neurological aging and reduce learning capabilities. This is likely mediated by the augmentation of circulatory factors that compromise vascular and blood-brain barrier integrity, induce chronic neuroinflammation, and promote age-associated proteinopathy-related outcomes. Moreover, wildfire smoke may induce a reduced metabolic, senescent cellular phenotype. Future interventions could potentially leverage combined anti-inflammatory and NAD + boosting compounds to counter these effects. This review underscores the critical need to study the intricate interplay between environmental factors and the biological mechanisms of aging to pave the way for effective interventions. Frontiers Media S.A. 2023-10-11 /pmc/articles/PMC10600394/ /pubmed/37900096 http://dx.doi.org/10.3389/ftox.2023.1267667 Text en Copyright © 2023 Scieszka, Bolt, McCormick, Brigman and Campen. 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 Toxicology
Scieszka, David
Bolt, Alicia M.
McCormick, Mark A.
Brigman, Jonathan L.
Campen, Matthew J.
Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
title Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
title_full Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
title_fullStr Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
title_full_unstemmed Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
title_short Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
title_sort aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
topic Toxicology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600394/
https://www.ncbi.nlm.nih.gov/pubmed/37900096
http://dx.doi.org/10.3389/ftox.2023.1267667
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