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Disabled homolog 2 controls macrophage phenotypic polarization and adipose tissue inflammation
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Disabled homolog 2 controls macrophage phenotypic polarization and adipose tissue inflammation
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Journal Article
Disabled homolog 2 controls macrophage phenotypic polarization and adipose tissue inflammation
2016
Overview
Acute and chronic tissue injury results in the generation of a myriad of environmental cues that macrophages respond to by changing their phenotype and function. This phenotypic regulation is critical for controlling tissue inflammation and resolution. Here, we have identified the adaptor protein disabled homolog 2 (DAB2) as a regulator of phenotypic switching in macrophages. Dab2 expression was upregulated in M2 macrophages and suppressed in M1 macrophages isolated from both mice and humans, and genetic deletion of Dab2 predisposed macrophages to adopt a proinflammatory M1 phenotype. In mice with myeloid cell-specific deletion of Dab2 (Dab2fl/fl Lysm-Cre), treatment with sublethal doses of LPS resulted in increased proinflammatory gene expression and macrophage activation. Moreover, chronic high-fat feeding exacerbated adipose tissue inflammation, M1 polarization of adipose tissue macrophages, and the development of insulin resistance in DAB2-deficient animals compared with controls. Mutational analyses revealed that DAB2 interacts with TNF receptor-associated factor 6 (TRAF6) and attenuates IκB kinase β-dependent (IKKβ-dependent) phosphorylation of Ser536 in the transactivation domain of NF-κB p65. Together, these findings reveal that DAB2 is critical for controlling inflammatory signaling during phenotypic polarization of macrophages and suggest that manipulation of DAB2 expression and function may hold therapeutic potential for the treatment of acute and chronic inflammatory disorders.
Publisher
American Society for Clinical Investigation
Subject
Adaptor Proteins, Signal Transducing - biosynthesis
/ Adaptor Proteins, Signal Transducing - genetics
/ Adaptor Proteins, Vesicular Transport - biosynthesis
/ Adaptor Proteins, Vesicular Transport - genetics
/ Animals
/ Body fat
/ Cellular signal transduction
/ Grants
/ Humans
/ I-kappa B Kinase - metabolism
/ Intracellular Signaling Peptides and Proteins - genetics
/ Intracellular Signaling Peptides and Proteins - metabolism
/ Kinases
/ Ligands
/ Mice
/ Neoplasm Proteins - genetics
/ Neoplasm Proteins - metabolism
/ Software
/ Transcription Factor RelA - genetics
/ Transcription Factor RelA - metabolism
