Stearic Acid Induces CD11c Expression in Proinflammatory Macrophages via Epidermal Fatty Acid Binding Protein
Author(s) -
Jun Zeng,
Yuwen Zhang,
Jiaqing Hao,
Yanwen Sun,
Shujun Liu,
David Bernlohr,
Edward R. Sauter,
Margot P. Cleary,
Jill Suttles,
Bing Li
Publication year - 2018
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1701416
Subject(s) - proinflammatory cytokine , cd11c , downregulation and upregulation , chemistry , inflammation , stearic acid , macrophage , microbiology and biotechnology , biology , endocrinology , biochemistry , in vitro , immunology , phenotype , organic chemistry , gene
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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom