| Literature DB >> 29626089 |
Jun Zeng1,2, Yuwen Zhang1, Jiaqing Hao1, Yanwen Sun1, Shujun Liu3, David A Bernlohr4, Edward R Sauter5, Margot P Cleary3, Jill Suttles1, Bing Li6.
Abstract
Obesity is associated with elevated levels of free fatty acids (FAs) and proinflammatory CD11c+ macrophages. However, whether and how free FAs contribute to CD11c+ macrophage differentiation and proinflammatory functions remain unclear. Here we report that dietary saturated FAs, but not unsaturated FAs, promoted the differentiation and function of CD11c+ macrophages. Specifically, we demonstrated that stearic acid (SA) significantly induced CD11c expression in monocytes through activation of the nuclear retinoid acid receptor. More importantly, cytosolic expression of epidermal FA binding protein (E-FABP) in monocytes/macrophages was shown to be critical to the mediation of the SA-induced effect. Depletion of E-FABP not only inhibited SA-induced CD11c upregulation in macrophages in vitro but also abrogated high-saturated-fat diet-induced skin lesions in obese mouse models in vivo. Altogether, our data demonstrate a novel mechanism by which saturated FAs promote obesity-associated inflammation through inducing E-FABP/retinoid acid receptor-mediated differentiation of CD11c+ macrophages.Entities:
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Year: 2018 PMID: 29626089 PMCID: PMC5940522 DOI: 10.4049/jimmunol.1701416
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422