Switzer Kirsten C, Fan Yang-Yi, Wang Naisyin, McMurray David N, Chapkin Robert S
Molecular and Cell Biology Section, Faculty of Nutrition, Texas A&M University, College Station, TX, USA.
J Lipid Res. 2004 Aug;45(8):1482-92. doi: 10.1194/jlr.M400028-JLR200. Epub 2004 May 16.
Dietary n-3 PUFAs have been shown to attenuate T-cell-mediated inflammation. To investigate whether dietary n-3 PUFAs promote activation-induced cell death (AICD) in CD4+ T-cells induced in vitro to a polarized T-helper1 (Th1) phenotype, C57BL/6 mice were fed diets containing either 5% corn oil (CO; n-6 PUFA control) or 4% fish oil (FO) plus 1% CO (n-3 PUFA) for 2 weeks. Splenic CD4+ T-cells were cultured with alpha-interleukin-4 (alphaIL-4), IL-12, and IL-2 for 2 days and then with recombinant (r) IL-12 and rIL-2 for 3 days in the presence of diet-matched homologous mouse serum (HMS) to prevent loss of cell membrane fatty acids, or with fetal bovine serum. After polarization, Th1 cells were reactivated and analyzed for interferon-gamma and IL-4 by intracellular cytokine staining and for apoptosis by Annexin V/propidium iodide. Dietary FO enhanced Th1 polarization by 49% (P = 0.0001) and AICD by 24% (P = 0.0001) only in cells cultured in the presence of HMS. FO enhancement of Th1 polarization and AICD after culture was associated with the maintenance of eicosapentaenoic acid (20:5n-3) and docosahexaenoic acid (22:6n-3) in plasma membrane lipid rafts. In conclusion, n-3 PUFAs enhance the polarization and deletion of proinflammatory Th1 cells, possibly as a result of alterations in membrane microdomain fatty acid composition.
膳食中的n-3多不饱和脂肪酸(PUFAs)已被证明可减轻T细胞介导的炎症。为了研究膳食n-3 PUFAs是否能促进体外诱导为极化T辅助1(Th1)表型的CD4+ T细胞中的活化诱导细胞死亡(AICD),给C57BL/6小鼠喂食含5%玉米油(CO;n-6 PUFA对照)或4%鱼油(FO)加1% CO(n-3 PUFA)的饮食2周。脾CD4+ T细胞先用α-白细胞介素-4(αIL-4)、IL-12和IL-2培养2天,然后在饮食匹配的同源小鼠血清(HMS)存在下用重组(r)IL-12和rIL-2培养3天,以防止细胞膜脂肪酸丢失,或用胎牛血清培养。极化后,重新激活Th1细胞,并通过细胞内细胞因子染色分析干扰素-γ和IL-4,通过膜联蛋白V/碘化丙啶分析细胞凋亡。仅在HMS存在下培养的细胞中,膳食FO使Th1极化增强49%(P = 0.0001),AICD增强24%(P = 0.0001)。培养后FO对Th1极化和AICD的增强与质膜脂筏中二十碳五烯酸(20:5n-3)和二十二碳六烯酸(22:6n-3)的维持有关。总之,n-3 PUFAs可能由于膜微区脂肪酸组成的改变而增强促炎性Th1细胞的极化和清除。