促炎细胞因子
CD11c公司
下调和上调
化学
炎症
硬脂酸
巨噬细胞
细胞生物学
生物
内分泌学
生物化学
体外
免疫学
表型
基因
有机化学
作者
Jun Zeng,Yuwen Zhang,Jiaqing Hao,Yanwen Sun,Shujun Liu,David Bernlohr,Edward R. Sauter,Margot P. Cleary,Jill Suttles,Bing Li
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2018-04-06
卷期号:200 (10): 3407-3419
被引量:39
标识
DOI:10.4049/jimmunol.1701416
摘要
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.
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