Soni Nikul K, Ross Alastair B, Scheers Nathalie, Savolainen Otto I, Nookaew Intawat, Gabrielsson Britt G, Sandberg Ann-Sofie
Division of Food and Nutrition Science, Department of Biology and Biological Engineering, Chalmers University of Technology, SE-41296 Gothenburg, Sweden.
Division of Systems and Synthetic Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, SE-41296 Gothenburg, Sweden.
Nutrients. 2017 Jan 10;9(1):50. doi: 10.3390/nu9010050.
Dietary -3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) are associated with reduction of inflammation, although the mechanisms are poorly understood, especially how the spleen, as a secondary lymphoid organ, is involved. To investigate the effects of EPA and DHA on spleen gene expression, male C57BL/6J mice were fed high fat diets (HFD) differing in fatty acid composition, either based on corn oil (HFD-CO), or CO enriched with 2 g/100 g EPA and DHA (HFD-ED), for eight weeks. Spleen tissue was analyzed using transcriptomics and for fatty acids profiling. Biological processes (BPs) related to the immune response, including T-cell receptor signaling pathway, T-cell differentiation and co-stimulation, myeloid dendritic cell differentiation, antigen presentation and processing, and the toll like receptor pathway were downregulated by HFD-ED compared with control and HFD-CO. These findings were supported by the down-regulation of NF-κB in HFD-ED compared with HFD-CO fed mice. Lower phospholipid arachidonic acid levels in HFD-ED compared with HFD-CO, and control mice suggest attenuation of pathways via prostaglandins and leukotrienes. The HFD-ED also upregulated BPs related to erythropoiesis and hematopoiesis compared with control and HFD-CO fed mice. Our findings suggest that EPA and DHA down-regulate the splenic immune response induced by HFD-CO, supporting earlier work that the spleen is a target organ for the anti-inflammatory effects of these -3 fatty acids.
膳食中的ω-3脂肪酸二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)与炎症减轻有关,尽管其机制尚不清楚,尤其是作为二级淋巴器官的脾脏如何参与其中。为了研究EPA和DHA对脾脏基因表达的影响,将雄性C57BL/6J小鼠喂食脂肪酸组成不同的高脂肪饮食(HFD),一种基于玉米油(HFD-CO),另一种是富含2 g/100 g EPA和DHA的玉米油(HFD-ED),持续八周。使用转录组学和脂肪酸谱分析对脾脏组织进行分析。与对照和HFD-CO相比,HFD-ED下调了与免疫反应相关的生物学过程(BP),包括T细胞受体信号通路、T细胞分化和共刺激、髓样树突状细胞分化、抗原呈递和加工以及Toll样受体途径。与喂食HFD-CO的小鼠相比,HFD-ED中NF-κB的下调支持了这些发现。与HFD-CO和对照小鼠相比,HFD-ED中较低的磷脂花生四烯酸水平表明通过前列腺素和白三烯的途径减弱。与对照和喂食HFD-CO的小鼠相比,HFD-ED还上调了与红细胞生成和造血相关的BP。我们的研究结果表明,EPA和DHA下调了HFD-CO诱导的脾脏免疫反应,支持了早期的研究工作,即脾脏是这些ω-3脂肪酸抗炎作用的靶器官。