Chapkin R S, Arrington J L, Apanasovich T V, Carroll R J, McMurray D N
Faculty of Nutrition, Center for Environmental and Rural, Health and Department of Statistics, Texas 77843-1114, USA.
Clin Exp Immunol. 2002 Oct;130(1):12-8. doi: 10.1046/j.1365-2249.2002.01951.x.
Diets enriched in n-3 polyunsaturated fatty acids (PUFA) suppress several functions of murine splenic T cells by acting directly on the T cells and/or indirectly on accessory cells. In this study, the relative contribution of highly purified populations of the two cell types to the dietary suppression of T cell function was examined. Mice were fed diets containing different levels of n-3 PUFA; safflower oil (SAF; control containing no n-3 PUFA), fish oil (FO) at 2% and 4%, or 1% purified docosahexaenoic acid (DHA) for 2 weeks. Purified (>90%) T cells were obtained from the spleen, and accessory cells (>95% adherent, esterase-positive) were obtained by peritoneal lavage. Purified T cells or accessory cells from each diet group were co-cultured with the alternative cell type from every other diet group, yielding a total of 16 different co-culture combinations. The T cells were stimulated with either concanavalin A (ConA) or antibodies to the T cell receptor (TcR)/CD3 complex and the costimulatory molecule CD28 (alphaCD3/alphaCD28), and proliferation was measured after four days. Suppression of T cell proliferation in the co-cultures was dependent upon the dose of dietary n-3 PUFA fed to mice from which the T cells were derived, irrespective of the dietary treatment of accessory cell donors. The greatest dietary effect was seen in mice consuming the DHA diet (P = 0.034 in the anova; P=0.0053 in the Trend Test), and was observed with direct stimulation of the T cell receptor and CD28 costimulatory ligand, but not with ConA. A significant dietary effect was also contributed accessory cells (P = 0.033 in the Trend Test). We conclude that dietary n-3 PUFA affect TcR-mediated by T cell activation by both direct and indirect (accessory cell) mechanisms.
富含n-3多不饱和脂肪酸(PUFA)的饮食通过直接作用于T细胞和/或间接作用于辅助细胞来抑制小鼠脾脏T细胞的多种功能。在本研究中,研究了这两种细胞类型的高度纯化群体对饮食抑制T细胞功能的相对贡献。给小鼠喂食含有不同水平n-3 PUFA的饮食;红花油(SAF;不含n-3 PUFA的对照)、2%和4%的鱼油(FO)或1%的纯化二十二碳六烯酸(DHA),持续2周。从脾脏中获得纯化的(>90%)T细胞,并通过腹腔灌洗获得辅助细胞(>95%贴壁,酯酶阳性)。将每个饮食组的纯化T细胞或辅助细胞与其他每个饮食组的另一种细胞类型共培养,总共产生16种不同的共培养组合。用刀豆蛋白A(ConA)或针对T细胞受体(TcR)/CD3复合物和共刺激分子CD28(αCD3/αCD28)的抗体刺激T细胞,并在四天后测量增殖。共培养中T细胞增殖的抑制取决于喂食T细胞来源小鼠的饮食中n-3 PUFA的剂量,而与辅助细胞供体的饮食处理无关。在食用DHA饮食的小鼠中观察到最大的饮食效应(方差分析中P = 0.034;趋势检验中P = 0.0053),并且在直接刺激T细胞受体和CD28共刺激配体时观察到,但用ConA刺激时未观察到。辅助细胞也对饮食有显著影响(趋势检验中P = 0.033)。我们得出结论,饮食中的n-3 PUFA通过直接和间接(辅助细胞)机制影响TcR介导的T细胞活化。