Jenski L J, Bowker G M, Johnson M A, Ehringer W D, Fetterhoff T, Stillwell W
Department of Biology, Indiana University-Purdue University at Indianapolis, IN 46202-5132, USA.
Biochim Biophys Acta. 1995 May 24;1236(1):39-50. doi: 10.1016/0005-2736(95)00034-z.
Here we test whether the incorporation of docosahexaenoic acid (DHA, 22:6), an (n-3) fatty acid, into lymphocyte membranes affects the expression of the surface proteins Thy-1.2 and CD8. DHA was incorporated into splenocytes by three methods: feeding mice diets containing menhaden (fish) oil, fusing splenocytes with DHA-containing phosphatidylcholine vesicles, and culturing splenocytes with DHA. Thy-1.2 and CD8 expression were measured by flow cytometry and complement-mediated lysis using a panel of monoclonal antibodies. As (n-3) fatty acid incorporation into the lymphocytes increased, the expression of one Thy-1.2 epitope and one CD8 epitope decreased; the expression of two CD8 epitopes increased. Although diet-induced changes in surface protein expression may result from selective migration of cell populations or the diet's effect on protein biosynthesis, fusion with lipid vesicles demonstrated that DHA-containing phospholipids can mediate a direct and immediate effect. The decrease in Thy-1.2 expression was sustained for more than a week after removal of (n-3) fatty acids from the diet, most likely due to retention of membrane-bound (n-3) fatty acids. Because Thy-1.2 and CD8 participate in T cell activation, modulation of their expression by DHA suggests that DHA, when serving as a membrane structural element, may alter immune function.
在此,我们测试将一种(n - 3)脂肪酸二十二碳六烯酸(DHA,22:6)掺入淋巴细胞膜中是否会影响表面蛋白Thy - 1.2和CD8的表达。通过三种方法将DHA掺入脾细胞:给小鼠喂食含鲱鱼油的饮食、将脾细胞与含DHA的磷脂酰胆碱囊泡融合,以及用DHA培养脾细胞。使用一组单克隆抗体,通过流式细胞术和补体介导的细胞溶解来测量Thy - 1.2和CD8的表达。随着淋巴细胞中(n - 3)脂肪酸掺入量的增加,一个Thy - 1.2表位和一个CD8表位的表达降低;两个CD8表位的表达增加。尽管饮食诱导的表面蛋白表达变化可能是由于细胞群体的选择性迁移或饮食对蛋白质生物合成的影响,但与脂质囊泡的融合表明含DHA的磷脂可以介导直接且即时的效应。从饮食中去除(n - 3)脂肪酸后,Thy - 1.2表达的降低持续了一周多,这很可能是由于膜结合的(n - 3)脂肪酸的保留。由于Thy - 1.2和CD8参与T细胞活化,DHA对它们表达的调节表明,当DHA作为膜结构元件时,可能会改变免疫功能。