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The M1 and M2 paradigm of macrophage activation: time for reassessment

Macrophages are endowed with a variety of receptors for lineage-determining growth factors, T helper (Th) cell cytokines, and B cell, host, and microbial products. In tissues, macrophages mature and are activated in a dynamic response to combinations of these stimuli to acquire specialized functiona...

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Detalles Bibliográficos
Autores principales: Martinez, Fernando O., Gordon, Siamon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculty of 1000 Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944738/
https://www.ncbi.nlm.nih.gov/pubmed/24669294
http://dx.doi.org/10.12703/P6-13
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author Martinez, Fernando O.
Gordon, Siamon
author_facet Martinez, Fernando O.
Gordon, Siamon
author_sort Martinez, Fernando O.
collection PubMed
description Macrophages are endowed with a variety of receptors for lineage-determining growth factors, T helper (Th) cell cytokines, and B cell, host, and microbial products. In tissues, macrophages mature and are activated in a dynamic response to combinations of these stimuli to acquire specialized functional phenotypes. As for the lymphocyte system, a dichotomy has been proposed for macrophage activation: classic vs. alternative, also M1 and M2, respectively. In view of recent research about macrophage functions and the increasing number of immune-relevant ligands, a revision of the model is needed. Here, we assess how cytokines and pathogen signals influence their functional phenotypes and the evidence for M1 and M2 functions and revisit a paradigm initially based on the role of a restricted set of selected ligands in the immune response.
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spelling pubmed-39447382014-03-25 The M1 and M2 paradigm of macrophage activation: time for reassessment Martinez, Fernando O. Gordon, Siamon F1000Prime Rep Review Article Macrophages are endowed with a variety of receptors for lineage-determining growth factors, T helper (Th) cell cytokines, and B cell, host, and microbial products. In tissues, macrophages mature and are activated in a dynamic response to combinations of these stimuli to acquire specialized functional phenotypes. As for the lymphocyte system, a dichotomy has been proposed for macrophage activation: classic vs. alternative, also M1 and M2, respectively. In view of recent research about macrophage functions and the increasing number of immune-relevant ligands, a revision of the model is needed. Here, we assess how cytokines and pathogen signals influence their functional phenotypes and the evidence for M1 and M2 functions and revisit a paradigm initially based on the role of a restricted set of selected ligands in the immune response. Faculty of 1000 Ltd 2014-03-03 /pmc/articles/PMC3944738/ /pubmed/24669294 http://dx.doi.org/10.12703/P6-13 Text en © 2014 Faculty of 1000 Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode All F1000Prime Reports articles are distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Martinez, Fernando O.
Gordon, Siamon
The M1 and M2 paradigm of macrophage activation: time for reassessment
title The M1 and M2 paradigm of macrophage activation: time for reassessment
title_full The M1 and M2 paradigm of macrophage activation: time for reassessment
title_fullStr The M1 and M2 paradigm of macrophage activation: time for reassessment
title_full_unstemmed The M1 and M2 paradigm of macrophage activation: time for reassessment
title_short The M1 and M2 paradigm of macrophage activation: time for reassessment
title_sort m1 and m2 paradigm of macrophage activation: time for reassessment
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944738/
https://www.ncbi.nlm.nih.gov/pubmed/24669294
http://dx.doi.org/10.12703/P6-13
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