Macrophages, Meta-Inflammation, and Immuno-Metabolism

Current research depicts specific modes of immunity and energy metabolism as being interrelated at the molecular, cellular, organ and organism level. Hence, whereas M2 (alternatively-activated) macrophages dominate insulin-sensitive adipose tissue in the lean, M1-skewed (classically-activated) macro...

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Main Authors: Haim Shapiro, Aviv Lutaty, Amiram Ariel
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/2011/397971
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spelling doaj-9ee5a5a1086745dd8e878e26e0c175312020-11-25T02:14:10ZengHindawi LimitedThe Scientific World Journal1537-744X2011-01-01112509252910.1100/2011/397971397971Macrophages, Meta-Inflammation, and Immuno-MetabolismHaim Shapiro0Aviv Lutaty1Amiram Ariel2Department of Biology, Faculty of Natural Sciences, University of Haifa, Haifa 31905, IsraelDepartment of Biology, Faculty of Natural Sciences, University of Haifa, Haifa 31905, IsraelDepartment of Biology, Faculty of Natural Sciences, University of Haifa, Haifa 31905, IsraelCurrent research depicts specific modes of immunity and energy metabolism as being interrelated at the molecular, cellular, organ and organism level. Hence, whereas M2 (alternatively-activated) macrophages dominate insulin-sensitive adipose tissue in the lean, M1-skewed (classically-activated) macrophages accumulate in parallel to adiposity in the obese, and promote inflammation and insulin resistance, that is, meta-inflammation. The latest frontier of immuno-metabolism explores the coregulation of energy metabolism and immune function within hematopoietic cells. M1-skewed macrophages are sustained in edematous, hypoxic tissues by anaerobic glycolysis, whereas mitochondrial biogenesis and respiration dominates in M2 cells. We review the underlying mechanisms and the consequences of the transition from M2 to M1 predominance in adipose tissue, as well as the extracellular signals and transcription factors that control macrophage phenotypes and impose distinct metabolic modes.http://dx.doi.org/10.1100/2011/397971
collection DOAJ
language English
format Article
sources DOAJ
author Haim Shapiro
Aviv Lutaty
Amiram Ariel
spellingShingle Haim Shapiro
Aviv Lutaty
Amiram Ariel
Macrophages, Meta-Inflammation, and Immuno-Metabolism
The Scientific World Journal
author_facet Haim Shapiro
Aviv Lutaty
Amiram Ariel
author_sort Haim Shapiro
title Macrophages, Meta-Inflammation, and Immuno-Metabolism
title_short Macrophages, Meta-Inflammation, and Immuno-Metabolism
title_full Macrophages, Meta-Inflammation, and Immuno-Metabolism
title_fullStr Macrophages, Meta-Inflammation, and Immuno-Metabolism
title_full_unstemmed Macrophages, Meta-Inflammation, and Immuno-Metabolism
title_sort macrophages, meta-inflammation, and immuno-metabolism
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2011-01-01
description Current research depicts specific modes of immunity and energy metabolism as being interrelated at the molecular, cellular, organ and organism level. Hence, whereas M2 (alternatively-activated) macrophages dominate insulin-sensitive adipose tissue in the lean, M1-skewed (classically-activated) macrophages accumulate in parallel to adiposity in the obese, and promote inflammation and insulin resistance, that is, meta-inflammation. The latest frontier of immuno-metabolism explores the coregulation of energy metabolism and immune function within hematopoietic cells. M1-skewed macrophages are sustained in edematous, hypoxic tissues by anaerobic glycolysis, whereas mitochondrial biogenesis and respiration dominates in M2 cells. We review the underlying mechanisms and the consequences of the transition from M2 to M1 predominance in adipose tissue, as well as the extracellular signals and transcription factors that control macrophage phenotypes and impose distinct metabolic modes.
url http://dx.doi.org/10.1100/2011/397971
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AT avivlutaty macrophagesmetainflammationandimmunometabolism
AT amiramariel macrophagesmetainflammationandimmunometabolism
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