Autophagy of naïve CD4+T cells in aging - The role of body adiposity and physical fitness
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , |
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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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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1826304482974105600 |