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Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization
Macrophages play important roles in conditions ranging from host immune defense to tissue regeneration and polarize their functional phenotype accordingly. Next to differences in the use of L-arginine and the production of different cytokines, inflammatory M1 macrophages and anti-inflammatory M2 mac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052297/ https://www.ncbi.nlm.nih.gov/pubmed/32158446 http://dx.doi.org/10.3389/fimmu.2020.00152 |
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author | Wentzel, Annelieke S. Janssen, Joëlle J. E. de Boer, Vincent C. J. van Veen, Wouter G. Forlenza, Maria Wiegertjes, Geert F. |
author_facet | Wentzel, Annelieke S. Janssen, Joëlle J. E. de Boer, Vincent C. J. van Veen, Wouter G. Forlenza, Maria Wiegertjes, Geert F. |
author_sort | Wentzel, Annelieke S. |
collection | PubMed |
description | Macrophages play important roles in conditions ranging from host immune defense to tissue regeneration and polarize their functional phenotype accordingly. Next to differences in the use of L-arginine and the production of different cytokines, inflammatory M1 macrophages and anti-inflammatory M2 macrophages are also metabolically distinct. In mammals, M1 macrophages show metabolic reprogramming toward glycolysis, while M2 macrophages rely on oxidative phosphorylation to generate energy. The presence of polarized functional immune phenotypes conserved from mammals to fish led us to hypothesize that a similar metabolic reprogramming in polarized macrophages exists in carp. We studied mitochondrial function of M1 and M2 carp macrophages under basal and stressed conditions to determine oxidative capacity by real-time measurements of oxygen consumption and glycolytic capacity by measuring lactate-based acidification. In M1 macrophages, we found increased nitric oxide production and irg1 expression in addition to altered oxidative phosphorylation and glycolysis. In M2 macrophages, we found increased arginase activity, and both oxidative phosphorylation and glycolysis were similar to control macrophages. These results indicate that M1 and M2 carp macrophages show distinct metabolic signatures and indicate that metabolic reprogramming may occur in carp M1 macrophages. This immunometabolic reprogramming likely supports the inflammatory phenotype of polarized macrophages in teleost fish such as carp, similar to what has been shown in mammals. |
format | Online Article Text |
id | pubmed-7052297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70522972020-03-10 Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization Wentzel, Annelieke S. Janssen, Joëlle J. E. de Boer, Vincent C. J. van Veen, Wouter G. Forlenza, Maria Wiegertjes, Geert F. Front Immunol Immunology Macrophages play important roles in conditions ranging from host immune defense to tissue regeneration and polarize their functional phenotype accordingly. Next to differences in the use of L-arginine and the production of different cytokines, inflammatory M1 macrophages and anti-inflammatory M2 macrophages are also metabolically distinct. In mammals, M1 macrophages show metabolic reprogramming toward glycolysis, while M2 macrophages rely on oxidative phosphorylation to generate energy. The presence of polarized functional immune phenotypes conserved from mammals to fish led us to hypothesize that a similar metabolic reprogramming in polarized macrophages exists in carp. We studied mitochondrial function of M1 and M2 carp macrophages under basal and stressed conditions to determine oxidative capacity by real-time measurements of oxygen consumption and glycolytic capacity by measuring lactate-based acidification. In M1 macrophages, we found increased nitric oxide production and irg1 expression in addition to altered oxidative phosphorylation and glycolysis. In M2 macrophages, we found increased arginase activity, and both oxidative phosphorylation and glycolysis were similar to control macrophages. These results indicate that M1 and M2 carp macrophages show distinct metabolic signatures and indicate that metabolic reprogramming may occur in carp M1 macrophages. This immunometabolic reprogramming likely supports the inflammatory phenotype of polarized macrophages in teleost fish such as carp, similar to what has been shown in mammals. Frontiers Media S.A. 2020-02-25 /pmc/articles/PMC7052297/ /pubmed/32158446 http://dx.doi.org/10.3389/fimmu.2020.00152 Text en Copyright © 2020 Wentzel, Janssen, de Boer, van Veen, Forlenza and Wiegertjes. http://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 Wentzel, Annelieke S. Janssen, Joëlle J. E. de Boer, Vincent C. J. van Veen, Wouter G. Forlenza, Maria Wiegertjes, Geert F. Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization |
title | Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization |
title_full | Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization |
title_fullStr | Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization |
title_full_unstemmed | Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization |
title_short | Fish Macrophages Show Distinct Metabolic Signatures Upon Polarization |
title_sort | fish macrophages show distinct metabolic signatures upon polarization |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052297/ https://www.ncbi.nlm.nih.gov/pubmed/32158446 http://dx.doi.org/10.3389/fimmu.2020.00152 |
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