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Markers of the ageing macrophage: a systematic review and meta-analysis

INTRODUCTION: Ageing research is establishing macrophages as key immune system regulators that undergo functional decline. Due to heterogeneity between species and tissue populations, a plethora of data exist and the power of scientific conclusions can vary substantially. This meta-analysis by infor...

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Autores principales: Moss, Charlotte E., Phipps, Hew, Wilson, Heather L., Kiss-Toth, Endre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373068/
https://www.ncbi.nlm.nih.gov/pubmed/37520567
http://dx.doi.org/10.3389/fimmu.2023.1222308
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author Moss, Charlotte E.
Phipps, Hew
Wilson, Heather L.
Kiss-Toth, Endre
author_facet Moss, Charlotte E.
Phipps, Hew
Wilson, Heather L.
Kiss-Toth, Endre
author_sort Moss, Charlotte E.
collection PubMed
description INTRODUCTION: Ageing research is establishing macrophages as key immune system regulators that undergo functional decline. Due to heterogeneity between species and tissue populations, a plethora of data exist and the power of scientific conclusions can vary substantially. This meta-analysis by information content (MAIC) and systematic literature review (SLR) aims to determine overall changes in macrophage gene and protein expression, as well as function, with age. METHODS: PubMed was utilized to collate peer-reviewed literature relating to macrophage ageing. Primary studies comparing macrophages in at least two age groups were included. Data pertaining to gene or protein expression alongside method used were extracted for MAIC analysis. For SLR analysis, data included all macrophage-specific changes with age, as well as species, ontogeny and age of groups assessed. RESULTS: A total of 240 studies were included; 122 of which qualified for MAIC. The majority of papers focussed on changes in macrophage count/infiltration as a function of age, followed by gene and protein expression. The MAIC found iNOS and TNF to be the most commonly investigated entities, with 328 genes and 175 proteins showing consistent dysregulation with age across the literature. Overall findings indicate that cytokine secretion and phagocytosis are reduced and reactive oxygen species production is increased in the ageing macrophage. DISCUSSION: Collectively, our analysis identifies critical regulators in macrophage ageing that are consistently dysregulated, highlighting a plethora of targets for further investigation. Consistent functional changes with age found here can be used to confirm an ageing macrophage phenotype in specific studies and experimental models.
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spelling pubmed-103730682023-07-28 Markers of the ageing macrophage: a systematic review and meta-analysis Moss, Charlotte E. Phipps, Hew Wilson, Heather L. Kiss-Toth, Endre Front Immunol Immunology INTRODUCTION: Ageing research is establishing macrophages as key immune system regulators that undergo functional decline. Due to heterogeneity between species and tissue populations, a plethora of data exist and the power of scientific conclusions can vary substantially. This meta-analysis by information content (MAIC) and systematic literature review (SLR) aims to determine overall changes in macrophage gene and protein expression, as well as function, with age. METHODS: PubMed was utilized to collate peer-reviewed literature relating to macrophage ageing. Primary studies comparing macrophages in at least two age groups were included. Data pertaining to gene or protein expression alongside method used were extracted for MAIC analysis. For SLR analysis, data included all macrophage-specific changes with age, as well as species, ontogeny and age of groups assessed. RESULTS: A total of 240 studies were included; 122 of which qualified for MAIC. The majority of papers focussed on changes in macrophage count/infiltration as a function of age, followed by gene and protein expression. The MAIC found iNOS and TNF to be the most commonly investigated entities, with 328 genes and 175 proteins showing consistent dysregulation with age across the literature. Overall findings indicate that cytokine secretion and phagocytosis are reduced and reactive oxygen species production is increased in the ageing macrophage. DISCUSSION: Collectively, our analysis identifies critical regulators in macrophage ageing that are consistently dysregulated, highlighting a plethora of targets for further investigation. Consistent functional changes with age found here can be used to confirm an ageing macrophage phenotype in specific studies and experimental models. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10373068/ /pubmed/37520567 http://dx.doi.org/10.3389/fimmu.2023.1222308 Text en Copyright © 2023 Moss, Phipps, Wilson and Kiss-Toth 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
Moss, Charlotte E.
Phipps, Hew
Wilson, Heather L.
Kiss-Toth, Endre
Markers of the ageing macrophage: a systematic review and meta-analysis
title Markers of the ageing macrophage: a systematic review and meta-analysis
title_full Markers of the ageing macrophage: a systematic review and meta-analysis
title_fullStr Markers of the ageing macrophage: a systematic review and meta-analysis
title_full_unstemmed Markers of the ageing macrophage: a systematic review and meta-analysis
title_short Markers of the ageing macrophage: a systematic review and meta-analysis
title_sort markers of the ageing macrophage: a systematic review and meta-analysis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373068/
https://www.ncbi.nlm.nih.gov/pubmed/37520567
http://dx.doi.org/10.3389/fimmu.2023.1222308
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