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The Metabolic Prospective and Redox Regulation of Macrophage Polarization

Macrophage plasticity is an important feature of these innate immune cells. Macrophage phenotypes are divided into two categories, the classically activated macrophages (CAM, M1 phenotype) and the alternatively activated macrophages (AAM, M2 phenotype). M1 macrophages are commonly associated with th...

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Detalles Bibliográficos
Autores principales: He, Chao, Carter, A Brent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780841/
https://www.ncbi.nlm.nih.gov/pubmed/26962470
http://dx.doi.org/10.4172/2155-9899.1000371
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author He, Chao
Carter, A Brent
author_facet He, Chao
Carter, A Brent
author_sort He, Chao
collection PubMed
description Macrophage plasticity is an important feature of these innate immune cells. Macrophage phenotypes are divided into two categories, the classically activated macrophages (CAM, M1 phenotype) and the alternatively activated macrophages (AAM, M2 phenotype). M1 macrophages are commonly associated with the generation of proinflammatory cytokines, whereas M2 macrophages are anti-inflammatory and often associated with tumor progression and fibrosis development. Macrophages produce high levels of reactive oxygen species (ROS). Recent evidence suggests ROS can potentially regulate macrophage phenotype. In addition, macrophages phenotypes are closely related to their metabolic patterns, particularly fatty acid/cholesterol metabolism. In this review, we briefly summarize recent advances in macrophage polarization with special attention to their relevance to specific disease conditions and metabolic regulation of polarization. Understanding these metabolic switches can facilitate the development of targeted therapies for various diseases.
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spelling pubmed-47808412016-03-07 The Metabolic Prospective and Redox Regulation of Macrophage Polarization He, Chao Carter, A Brent J Clin Cell Immunol Article Macrophage plasticity is an important feature of these innate immune cells. Macrophage phenotypes are divided into two categories, the classically activated macrophages (CAM, M1 phenotype) and the alternatively activated macrophages (AAM, M2 phenotype). M1 macrophages are commonly associated with the generation of proinflammatory cytokines, whereas M2 macrophages are anti-inflammatory and often associated with tumor progression and fibrosis development. Macrophages produce high levels of reactive oxygen species (ROS). Recent evidence suggests ROS can potentially regulate macrophage phenotype. In addition, macrophages phenotypes are closely related to their metabolic patterns, particularly fatty acid/cholesterol metabolism. In this review, we briefly summarize recent advances in macrophage polarization with special attention to their relevance to specific disease conditions and metabolic regulation of polarization. Understanding these metabolic switches can facilitate the development of targeted therapies for various diseases. 2015-11-30 2015-12 /pmc/articles/PMC4780841/ /pubmed/26962470 http://dx.doi.org/10.4172/2155-9899.1000371 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
He, Chao
Carter, A Brent
The Metabolic Prospective and Redox Regulation of Macrophage Polarization
title The Metabolic Prospective and Redox Regulation of Macrophage Polarization
title_full The Metabolic Prospective and Redox Regulation of Macrophage Polarization
title_fullStr The Metabolic Prospective and Redox Regulation of Macrophage Polarization
title_full_unstemmed The Metabolic Prospective and Redox Regulation of Macrophage Polarization
title_short The Metabolic Prospective and Redox Regulation of Macrophage Polarization
title_sort metabolic prospective and redox regulation of macrophage polarization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780841/
https://www.ncbi.nlm.nih.gov/pubmed/26962470
http://dx.doi.org/10.4172/2155-9899.1000371
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