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硬脂酸通过表皮脂肪酸结合蛋白诱导促炎巨噬细胞中 CD11c 的表达。

Stearic Acid Induces CD11c Expression in Proinflammatory Macrophages via Epidermal Fatty Acid Binding Protein.

机构信息

Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202.

School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, China 511436.

出版信息

J Immunol. 2018 May 15;200(10):3407-3419. doi: 10.4049/jimmunol.1701416. Epub 2018 Apr 6.

DOI:10.4049/jimmunol.1701416
PMID:29626089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5940522/
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.

摘要

肥胖与游离脂肪酸 (FAs) 水平升高和促炎的 CD11c 巨噬细胞有关。然而,游离脂肪酸是否以及如何促进 CD11c 巨噬细胞分化和促炎功能仍不清楚。在这里,我们报告饮食中的饱和脂肪酸,而不是不饱和脂肪酸,促进了 CD11c 巨噬细胞的分化和功能。具体来说,我们证明硬脂酸 (SA) 通过激活核视黄酸受体显著诱导单核细胞中 CD11c 的表达。更重要的是,我们表明单核细胞/巨噬细胞中胞质表皮 FA 结合蛋白 (E-FABP) 的表达对于介导 SA 诱导的作用至关重要。E-FABP 的耗竭不仅抑制了 SA 诱导的体外巨噬细胞中 CD11c 的上调,而且消除了肥胖小鼠模型中高饱和脂肪饮食诱导的皮肤损伤。总之,我们的数据表明,饱和脂肪酸通过诱导 E-FABP/视黄酸受体介导的 CD11c 巨噬细胞分化,促进肥胖相关炎症的一种新机制。

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