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The Metabolic Signature of Macrophage Responses

Macrophages are a heterogeneous population of immune cells playing several and diverse functions in homeostatic and immune responses. The broad spectrum of macrophage functions depends on both heterogeneity and plasticity of these cells, which are highly specialized in sensing the microenvironment a...

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Autores principales: Viola, Antonella, Munari, Fabio, Sánchez-Rodríguez, Ricardo, Scolaro, Tommaso, Castegna, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618143/
https://www.ncbi.nlm.nih.gov/pubmed/31333642
http://dx.doi.org/10.3389/fimmu.2019.01462
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author Viola, Antonella
Munari, Fabio
Sánchez-Rodríguez, Ricardo
Scolaro, Tommaso
Castegna, Alessandra
author_facet Viola, Antonella
Munari, Fabio
Sánchez-Rodríguez, Ricardo
Scolaro, Tommaso
Castegna, Alessandra
author_sort Viola, Antonella
collection PubMed
description Macrophages are a heterogeneous population of immune cells playing several and diverse functions in homeostatic and immune responses. The broad spectrum of macrophage functions depends on both heterogeneity and plasticity of these cells, which are highly specialized in sensing the microenvironment and modify their properties accordingly. Although it is clear that macrophage phenotypes are difficult to categorize and should be seen as plastic and adaptable, they can be simplified into two extremes: a pro-inflammatory (M1) and an anti-inflammatory/pro-resolving (M2) profile. Based on this definition, M1 macrophages are able to start and sustain inflammatory responses, secreting pro-inflammatory cytokines, activating endothelial cells, and inducing the recruitment of other immune cells into the inflamed tissue; on the other hand, M2 macrophages promote the resolution of inflammation, phagocytose apoptotic cells, drive collagen deposition, coordinate tissue integrity, and release anti-inflammatory mediators. Dramatic switches in cell metabolism accompany these phenotypic and functional changes of macrophages. In particular, M1 macrophages rely mainly on glycolysis and present two breaks on the TCA cycle that result in accumulation of itaconate (a microbicide compound) and succinate. Excess of succinate leads to Hypoxia Inducible Factor 1α (HIF1α) stabilization that, in turn, activates the transcription of glycolytic genes, thus sustaining the glycolytic metabolism of M1 macrophages. On the contrary, M2 cells are more dependent on oxidative phosphorylation (OXPHOS), their TCA cycle is intact and provides the substrates for the complexes of the electron transport chain (ETC). Moreover, pro- and anti-inflammatory macrophages are characterized by specific pathways that regulate the metabolism of lipids and amino acids and affect their responses. All these metabolic adaptations are functional to support macrophage activities as well as to sustain their polarization in specific contexts. The aim of this review is to discuss recent findings linking macrophage functions and metabolism.
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spelling pubmed-66181432019-07-22 The Metabolic Signature of Macrophage Responses Viola, Antonella Munari, Fabio Sánchez-Rodríguez, Ricardo Scolaro, Tommaso Castegna, Alessandra Front Immunol Immunology Macrophages are a heterogeneous population of immune cells playing several and diverse functions in homeostatic and immune responses. The broad spectrum of macrophage functions depends on both heterogeneity and plasticity of these cells, which are highly specialized in sensing the microenvironment and modify their properties accordingly. Although it is clear that macrophage phenotypes are difficult to categorize and should be seen as plastic and adaptable, they can be simplified into two extremes: a pro-inflammatory (M1) and an anti-inflammatory/pro-resolving (M2) profile. Based on this definition, M1 macrophages are able to start and sustain inflammatory responses, secreting pro-inflammatory cytokines, activating endothelial cells, and inducing the recruitment of other immune cells into the inflamed tissue; on the other hand, M2 macrophages promote the resolution of inflammation, phagocytose apoptotic cells, drive collagen deposition, coordinate tissue integrity, and release anti-inflammatory mediators. Dramatic switches in cell metabolism accompany these phenotypic and functional changes of macrophages. In particular, M1 macrophages rely mainly on glycolysis and present two breaks on the TCA cycle that result in accumulation of itaconate (a microbicide compound) and succinate. Excess of succinate leads to Hypoxia Inducible Factor 1α (HIF1α) stabilization that, in turn, activates the transcription of glycolytic genes, thus sustaining the glycolytic metabolism of M1 macrophages. On the contrary, M2 cells are more dependent on oxidative phosphorylation (OXPHOS), their TCA cycle is intact and provides the substrates for the complexes of the electron transport chain (ETC). Moreover, pro- and anti-inflammatory macrophages are characterized by specific pathways that regulate the metabolism of lipids and amino acids and affect their responses. All these metabolic adaptations are functional to support macrophage activities as well as to sustain their polarization in specific contexts. The aim of this review is to discuss recent findings linking macrophage functions and metabolism. Frontiers Media S.A. 2019-07-03 /pmc/articles/PMC6618143/ /pubmed/31333642 http://dx.doi.org/10.3389/fimmu.2019.01462 Text en Copyright © 2019 Viola, Munari, Sánchez-Rodríguez, Scolaro and Castegna. 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
Viola, Antonella
Munari, Fabio
Sánchez-Rodríguez, Ricardo
Scolaro, Tommaso
Castegna, Alessandra
The Metabolic Signature of Macrophage Responses
title The Metabolic Signature of Macrophage Responses
title_full The Metabolic Signature of Macrophage Responses
title_fullStr The Metabolic Signature of Macrophage Responses
title_full_unstemmed The Metabolic Signature of Macrophage Responses
title_short The Metabolic Signature of Macrophage Responses
title_sort metabolic signature of macrophage responses
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618143/
https://www.ncbi.nlm.nih.gov/pubmed/31333642
http://dx.doi.org/10.3389/fimmu.2019.01462
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