Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness

Detalhes bibliográficos
Autor(a) principal: Padilha, Camila S. [UNESP]
Data de Publicação: 2023
Outros Autores: Kushkestani, Mehdi, Baptista, Liliana P., Krüger, Karsten, Lira, Fábio Santos [UNESP]
Tipo de documento: Outros
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1017/erm.2023.2
http://hdl.handle.net/11449/248240
Resumo: Life expectancy has increased exponentially in the last century accompanied by disability, poor quality of life, and all-cause mortality in older age due to the high prevalence of obesity and physical inactivity in older people. Biologically, the aging process reduces the cell's metabolic and functional efficiency, and disrupts the cell's anabolic and catabolic homeostasis, predisposing older people to many dysfunctional conditions such as cardiovascular disease, neurodegenerative disorders, cancer, and diabetes. In the immune system, aging also alters cells' metabolic and functional efficiency, a process known as 'immunosenescence', where cells become more broadly inflammatory and their functionality is altered. Notably, autophagy, the conserved and important cellular process that maintains the cell's efficiency and functional homeostasis may protect the immune system from age-associated dysfunctional changes by regulating cell death in activated CD4+ T cells. This regulatory process increases the delivery of the dysfunctional cytoplasmic material to lysosomal degradation while increasing cytokine production, proliferation, and differentiation of CD4+ T cell-mediated immune responses. Poor proliferation and diminished responsiveness to cytokines appear to be ubiquitous features of aged T cells and may explain the delayed peak in T cell expansion and cytotoxic activity commonly observed in the 'immunosenescence' phenotype in the elderly. On the other hand, physical exercise stimulates the expression of crucial nutrient sensors and inhibits the mechanistic target of the rapamycin (mTOR) signaling cascade which increases autophagic activity in cells. Therefore, in this perspective review, we will first contextualize the overall view of the autophagy process and then, we will discuss how body adiposity and physical fitness may counteract autophagy in naïve CD4+ T cells in aging.
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spelling Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitnessAgeautophagynaïve cellsobesityphysical exerciseLife expectancy has increased exponentially in the last century accompanied by disability, poor quality of life, and all-cause mortality in older age due to the high prevalence of obesity and physical inactivity in older people. Biologically, the aging process reduces the cell's metabolic and functional efficiency, and disrupts the cell's anabolic and catabolic homeostasis, predisposing older people to many dysfunctional conditions such as cardiovascular disease, neurodegenerative disorders, cancer, and diabetes. In the immune system, aging also alters cells' metabolic and functional efficiency, a process known as 'immunosenescence', where cells become more broadly inflammatory and their functionality is altered. Notably, autophagy, the conserved and important cellular process that maintains the cell's efficiency and functional homeostasis may protect the immune system from age-associated dysfunctional changes by regulating cell death in activated CD4+ T cells. This regulatory process increases the delivery of the dysfunctional cytoplasmic material to lysosomal degradation while increasing cytokine production, proliferation, and differentiation of CD4+ T cell-mediated immune responses. Poor proliferation and diminished responsiveness to cytokines appear to be ubiquitous features of aged T cells and may explain the delayed peak in T cell expansion and cytotoxic activity commonly observed in the 'immunosenescence' phenotype in the elderly. On the other hand, physical exercise stimulates the expression of crucial nutrient sensors and inhibits the mechanistic target of the rapamycin (mTOR) signaling cascade which increases autophagic activity in cells. Therefore, in this perspective review, we will first contextualize the overall view of the autophagy process and then, we will discuss how body adiposity and physical fitness may counteract autophagy in naïve CD4+ T cells in aging.Exercise and Immunometabolism Research Group Post-graduation Program in Movement Sciences Department of Physical Education Universidade Estadual Paulista (UNESP), Presidente PrudenteWellness and Lifestyle Science Initiative Group PhD Student of Kinesiology and Health School of Art and Science Rutgers UniversityDepartment of Medicine Division of Gerontology Geriatrics Palliative Care Center for Exercise Medicine The University of Alabama at BirminghamResearch Center in Physical Activity Health and Leisure (CIAFEL) Faculty of Sports University of Porto (FADEUP)Laboratory for Integrative and Translational Research in Population Health (ITR)Department of Exercise Physiology and Sports Therapy Institute of Sports Science University of GiessenResearch Center for Sport and Physical Activity Faculty of Sports Science and Physical Education University of CoimbraExercise and Immunometabolism Research Group Post-graduation Program in Movement Sciences Department of Physical Education Universidade Estadual Paulista (UNESP), Presidente PrudenteUniversidade Estadual Paulista (UNESP)Rutgers UniversityThe University of Alabama at BirminghamUniversity of Porto (FADEUP)Laboratory for Integrative and Translational Research in Population Health (ITR)University of GiessenUniversity of CoimbraPadilha, Camila S. [UNESP]Kushkestani, MehdiBaptista, Liliana P.Krüger, KarstenLira, Fábio Santos [UNESP]2023-07-29T13:38:26Z2023-07-29T13:38:26Z2023-01-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/otherhttp://dx.doi.org/10.1017/erm.2023.2Expert Reviews in Molecular Medicine, v. 25.1462-3994http://hdl.handle.net/11449/24824010.1017/erm.2023.22-s2.0-85146666104Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengExpert Reviews in Molecular Medicineinfo:eu-repo/semantics/openAccess2024-06-18T17:43:15Zoai:repositorio.unesp.br:11449/248240Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-06-18T17:43:15Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
title Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
spellingShingle Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
Padilha, Camila S. [UNESP]
Age
autophagy
naïve cells
obesity
physical exercise
title_short Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
title_full Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
title_fullStr Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
title_full_unstemmed Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
title_sort Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
author Padilha, Camila S. [UNESP]
author_facet Padilha, Camila S. [UNESP]
Kushkestani, Mehdi
Baptista, Liliana P.
Krüger, Karsten
Lira, Fábio Santos [UNESP]
author_role author
author2 Kushkestani, Mehdi
Baptista, Liliana P.
Krüger, Karsten
Lira, Fábio Santos [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Rutgers University
The University of Alabama at Birmingham
University of Porto (FADEUP)
Laboratory for Integrative and Translational Research in Population Health (ITR)
University of Giessen
University of Coimbra
dc.contributor.author.fl_str_mv Padilha, Camila S. [UNESP]
Kushkestani, Mehdi
Baptista, Liliana P.
Krüger, Karsten
Lira, Fábio Santos [UNESP]
dc.subject.por.fl_str_mv Age
autophagy
naïve cells
obesity
physical exercise
topic Age
autophagy
naïve cells
obesity
physical exercise
description Life expectancy has increased exponentially in the last century accompanied by disability, poor quality of life, and all-cause mortality in older age due to the high prevalence of obesity and physical inactivity in older people. Biologically, the aging process reduces the cell's metabolic and functional efficiency, and disrupts the cell's anabolic and catabolic homeostasis, predisposing older people to many dysfunctional conditions such as cardiovascular disease, neurodegenerative disorders, cancer, and diabetes. In the immune system, aging also alters cells' metabolic and functional efficiency, a process known as 'immunosenescence', where cells become more broadly inflammatory and their functionality is altered. Notably, autophagy, the conserved and important cellular process that maintains the cell's efficiency and functional homeostasis may protect the immune system from age-associated dysfunctional changes by regulating cell death in activated CD4+ T cells. This regulatory process increases the delivery of the dysfunctional cytoplasmic material to lysosomal degradation while increasing cytokine production, proliferation, and differentiation of CD4+ T cell-mediated immune responses. Poor proliferation and diminished responsiveness to cytokines appear to be ubiquitous features of aged T cells and may explain the delayed peak in T cell expansion and cytotoxic activity commonly observed in the 'immunosenescence' phenotype in the elderly. On the other hand, physical exercise stimulates the expression of crucial nutrient sensors and inhibits the mechanistic target of the rapamycin (mTOR) signaling cascade which increases autophagic activity in cells. Therefore, in this perspective review, we will first contextualize the overall view of the autophagy process and then, we will discuss how body adiposity and physical fitness may counteract autophagy in naïve CD4+ T cells in aging.
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T13:38:26Z
2023-07-29T13:38:26Z
2023-01-19
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/other
format other
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1017/erm.2023.2
Expert Reviews in Molecular Medicine, v. 25.
1462-3994
http://hdl.handle.net/11449/248240
10.1017/erm.2023.2
2-s2.0-85146666104
url http://dx.doi.org/10.1017/erm.2023.2
http://hdl.handle.net/11449/248240
identifier_str_mv Expert Reviews in Molecular Medicine, v. 25.
1462-3994
10.1017/erm.2023.2
2-s2.0-85146666104
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Expert Reviews in Molecular Medicine
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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