Switzer Kirsten C, McMurray David N, Morris Jeffrey S, Chapkin Robert S
Molecular and Cell Biology Section, Faculty of Nutrition, Texas A&M University, College Station, TX, USA.
J Nutr. 2003 Feb;133(2):496-503. doi: 10.1093/jn/133.2.496.
Previous studies showing dietary (n-3) polyunsaturated fatty acids (PUFA) attenuate T cell immune-mediated inflammatory diseases led us to hypothesize that (n-3) PUFA promote activation-induced cell death (AICD) in T cells. Because T cell subsets display a differential resistance to AICD, we compared the effects of (n-3) PUFA feeding on T cells stimulated in vitro to express different cytokine profiles. Mice were fed either diets lacking (n-3) PUFA (control) or (n-3) PUFA-containing diets for 14 d. Splenic T cells were stimulated with alphaCD3/alphaCD28, phorbol myristate acetate (PMA)/Ionomycin or alphaCD3/PMA for 48 h, followed by reactivation with the same stimuli for 5 h. Apoptosis was measured using Annexin V/propidium iodide. (n-3) PUFA were selectively incorporated into membrane phospholipid pools. Cytokine analyses revealed that (n-3) PUFA enhanced AICD only in T cells expressing a T helper cell (Th)1-like cytokine profile after stimulation with PMA/Ionomycin compared to mice fed the (n-6) PUFA control diet (P = 0.0008). In contrast, no increase in apoptosis was seen in T cells stimulated with alphaCD3/PMA, which exhibited a Th2 cytokine profile. These data demonstrate that the ability of (n-3) PUFA to promote AICD is dependent on the activation stimulus. In conclusion, we have identified a novel mechanism by which (n-3) PUFA modulate T cell-mediated immunity by selective deletion of Th1-like cells while maintaining or enhancing the Th2-mediated humoral immune response.
以往的研究表明,膳食中的(n-3)多不饱和脂肪酸(PUFA)可减轻T细胞免疫介导的炎症性疾病,这使我们推测(n-3)PUFA可促进T细胞中的活化诱导细胞死亡(AICD)。由于T细胞亚群对AICD表现出不同的抗性,我们比较了喂食(n-3)PUFA对体外刺激以表达不同细胞因子谱的T细胞的影响。将小鼠喂食缺乏(n-3)PUFA的饮食(对照)或含(n-3)PUFA的饮食14天。用αCD3/αCD28、佛波酯肉豆蔻酸酯乙酸酯(PMA)/离子霉素或αCD3/PMA刺激脾T细胞48小时,然后用相同刺激物再激活5小时。使用膜联蛋白V/碘化丙啶测量细胞凋亡。(n-3)PUFA被选择性地整合到膜磷脂池中。细胞因子分析显示,与喂食(n-6)PUFA对照饮食的小鼠相比,(n-3)PUFA仅在PMA/离子霉素刺激后表达T辅助细胞(Th)1样细胞因子谱的T细胞中增强了AICD(P = 0.0008)。相反,在用αCD3/PMA刺激的T细胞中未观察到凋亡增加,这些T细胞表现出Th2细胞因子谱。这些数据表明,(n-3)PUFA促进AICD的能力取决于激活刺激。总之,我们确定了一种新机制,通过该机制(n-3)PUFA通过选择性删除Th1样细胞来调节T细胞介导的免疫,同时维持或增强Th2介导的体液免疫反应。