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Senescence-associated secretory phenotype and its impact on oral immune homeostasis
The senescence-associated secretory phenotype (SASP), which accumulates over the course of normal aging and in age-related diseases, is a crucial driver of chronic inflammation and aging phenotypes. It is also responsible for the pathogenesis of multiple oral diseases. However, the pathogenic mechan...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581398/ https://www.ncbi.nlm.nih.gov/pubmed/36275775 http://dx.doi.org/10.3389/fimmu.2022.1019313 |
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author | Yue, Ziqi Nie, Lulingxiao Zhao, Pengfei Ji, Ning Liao, Ga Wang, Qi |
author_facet | Yue, Ziqi Nie, Lulingxiao Zhao, Pengfei Ji, Ning Liao, Ga Wang, Qi |
author_sort | Yue, Ziqi |
collection | PubMed |
description | The senescence-associated secretory phenotype (SASP), which accumulates over the course of normal aging and in age-related diseases, is a crucial driver of chronic inflammation and aging phenotypes. It is also responsible for the pathogenesis of multiple oral diseases. However, the pathogenic mechanism underlying SASP has not yet been fully elucidated. Here, relevant articles on SASP published over the last five years (2017–2022) were retrieved and used for bibliometric analysis, for the first time, to examine SASP composition. More than half of the relevant articles focus on various cytokines (27.5%), growth factors (20.9%), and proteases (20.9%). In addition, lipid metabolites (13.1%) and extracellular vesicles (6.5%) have received increasing attention over the past five years, and have been recognized as novel SASP categories. Based on this, we summarize the evidences demonstrating that SASP plays a pleiotropic role in oral immunity and propose a four-step hypothetical framework for the progression of SASP-related oral pathology—1) oral SASP development, 2) SASP-related oral pathological alterations, 3) pathological changes leading to oral immune homeostasis disruption, and 4) SASP-mediated immune dysregulation escalating oral disease. By targeting specific SASP factors, potential therapies can be developed to treat oral and age-related diseases. |
format | Online Article Text |
id | pubmed-9581398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95813982022-10-20 Senescence-associated secretory phenotype and its impact on oral immune homeostasis Yue, Ziqi Nie, Lulingxiao Zhao, Pengfei Ji, Ning Liao, Ga Wang, Qi Front Immunol Immunology The senescence-associated secretory phenotype (SASP), which accumulates over the course of normal aging and in age-related diseases, is a crucial driver of chronic inflammation and aging phenotypes. It is also responsible for the pathogenesis of multiple oral diseases. However, the pathogenic mechanism underlying SASP has not yet been fully elucidated. Here, relevant articles on SASP published over the last five years (2017–2022) were retrieved and used for bibliometric analysis, for the first time, to examine SASP composition. More than half of the relevant articles focus on various cytokines (27.5%), growth factors (20.9%), and proteases (20.9%). In addition, lipid metabolites (13.1%) and extracellular vesicles (6.5%) have received increasing attention over the past five years, and have been recognized as novel SASP categories. Based on this, we summarize the evidences demonstrating that SASP plays a pleiotropic role in oral immunity and propose a four-step hypothetical framework for the progression of SASP-related oral pathology—1) oral SASP development, 2) SASP-related oral pathological alterations, 3) pathological changes leading to oral immune homeostasis disruption, and 4) SASP-mediated immune dysregulation escalating oral disease. By targeting specific SASP factors, potential therapies can be developed to treat oral and age-related diseases. Frontiers Media S.A. 2022-10-04 /pmc/articles/PMC9581398/ /pubmed/36275775 http://dx.doi.org/10.3389/fimmu.2022.1019313 Text en Copyright © 2022 Yue, Nie, Zhao, Ji, Liao and Wang 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 | Immunology Yue, Ziqi Nie, Lulingxiao Zhao, Pengfei Ji, Ning Liao, Ga Wang, Qi Senescence-associated secretory phenotype and its impact on oral immune homeostasis |
title | Senescence-associated secretory phenotype and its impact on oral immune homeostasis |
title_full | Senescence-associated secretory phenotype and its impact on oral immune homeostasis |
title_fullStr | Senescence-associated secretory phenotype and its impact on oral immune homeostasis |
title_full_unstemmed | Senescence-associated secretory phenotype and its impact on oral immune homeostasis |
title_short | Senescence-associated secretory phenotype and its impact on oral immune homeostasis |
title_sort | senescence-associated secretory phenotype and its impact on oral immune homeostasis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581398/ https://www.ncbi.nlm.nih.gov/pubmed/36275775 http://dx.doi.org/10.3389/fimmu.2022.1019313 |
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