Camacho-Muñoz Dolores, Niven Jennifer, Kucuk Salih, Cucchi Danilo, Certo Michelangelo, Jones Simon W, Fischer Deborah P, Mauro Claudio, Nicolaou Anna
Laboratory for Lipidomics and Lipid Biology, Division of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester M13 9PT, UK.
Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2WB, UK.
Biochem Pharmacol. 2022 Oct;204:115211. doi: 10.1016/j.bcp.2022.115211. Epub 2022 Aug 17.
Western diet (WD), high in sugar and fat, promotes obesity and associated chronic low-grade pro-inflammatory environment, leading to impaired immune function, reprogramming of innate and adaptive immune cells, and development of chronic degenerative diseases, including cardiovascular disease. Increased concentrations of circulating and tissue ceramides contribute to inflammation and cellular dysfunction common in immune metabolic and cardiometabolic disease. Therefore, ceramide-lowering interventions have been considered as strategies to improve adipose tissue health. Here, we report the ability of omega-3 polyunsaturated fatty acids (n-3PUFA) to attenuate inflammatory phenotypes promoted by WD, through ceramide-dependent pathways. Using an animal model, we show that enrichment of WD diet with n-3PUFA, reduced the expression of ceramide synthase 2 (CerS2), and lowered the concentration of long-chain ceramides (C23-C26) in plasma and adipose tissues. N-3PUFA also increased prevalence of the anti-inflammatory CD4Foxp3 and CD4Foxp3CD25 Treg subtypes in lymphoid organs. The CerS inhibitor FTY720 mirrored the effect of n-3PUFA. Treatment of animal and human T cells with ceramide C24 in vitro, reduced CD4Foxp3 Treg polarisation and IL-10 production, and increased IL-17, while it decreased Erk and Akt phosphorylation downstream of T cell antigen receptors (TCR). These findings suggest that molecular mechanisms mediating the adverse effect of ceramides on regulatory T lymphocytes, progress through reduced TCR signalling. Our findings suggest that nutritional enrichment of WD with fish oil n-3PUFA can partially mitigate its detrimental effects, potentially improving the low-grade inflammation associated with immune metabolic disease. Compared to pharmacological interventions, n-3PUFA offer a simpler approach that can be accommodated as lifestyle choice.
富含糖和脂肪的西方饮食(WD)会导致肥胖以及相关的慢性低度促炎环境,进而损害免疫功能,使先天性和适应性免疫细胞发生重编程,并引发包括心血管疾病在内的慢性退行性疾病。循环和组织中神经酰胺浓度的升高会导致免疫代谢和心脏代谢疾病中常见的炎症和细胞功能障碍。因此,降低神经酰胺的干预措施被视为改善脂肪组织健康的策略。在此,我们报告了ω-3多不饱和脂肪酸(n-3PUFA)通过神经酰胺依赖性途径减轻WD引发的炎症表型的能力。使用动物模型,我们发现WD饮食中添加n-3PUFA可降低神经酰胺合酶2(CerS2)的表达,并降低血浆和脂肪组织中长链神经酰胺(C23-C26)的浓度。n-3PUFA还增加了淋巴器官中抗炎性CD4Foxp3和CD4Foxp3CD25 Treg亚型的比例。神经酰胺合成酶抑制剂FTY720的作用与n-3PUFA类似。体外使用神经酰胺C24处理动物和人类T细胞,会降低CD4Foxp3 Treg极化和IL-10的产生,并增加IL-17,同时降低T细胞抗原受体(TCR)下游的Erk和Akt磷酸化。这些发现表明,神经酰胺对调节性T淋巴细胞产生不利影响的分子机制是通过减少TCR信号传导来实现的。我们的研究结果表明,用鱼油n-3PUFA对WD进行营养强化可以部分减轻其有害影响,有可能改善与免疫代谢疾病相关的低度炎症。与药物干预相比,n-3PUFA提供了一种更简单的方法,可以作为一种生活方式选择来采用。