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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculty of 1000 Ltd
2014
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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. |
format | Online Article Text |
id | pubmed-3944738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Faculty of 1000 Ltd |
record_format | MEDLINE/PubMed |
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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