Calder P C, Yaqoob P, Harvey D J, Watts A, Newsholme E A
Department of Biochemistry, University of Oxford, U.K.
Biochem J. 1994 Jun 1;300 ( Pt 2)(Pt 2):509-18. doi: 10.1042/bj3000509.
The fatty acid compositions of the neutral lipid and phospholipid fractions of rat lymph node lymphocytes were characterized. Stimulation of rat lymphocytes with the T-cell mitogen concanavalin A resulted in significant changes in the fatty acid composition of both neutral lipids and phospholipids (a decrease in the proportions of stearic, linoleic and arachidonic acids and an increase in the proportion of oleic acid). Membrane fluidity was measured using nitroxide spin-label e.s.r., and increased during culture with concanavalin A. Culturing the lymphocytes in the absence of mitogen did not affect fatty acid composition or membrane fluidity. The uptake and fate of palmitic, oleic, linoleic and arachidonic acids were studied in detail; there was a time-dependent incorporation of each fatty acid into all lipid classes but each fatty acid had a characteristic fate. Palmitic and arachidonic acids were incorporated principally into phospholipids whereas oleic and linoleic acids were incorporated in similar proportions into phospholipids and triacylglycerols. Oleic acid was incorporated mainly into phosphatidylcholine, palmitic and linoleic acids were incorporated equally into phosphatidylcholine and phosphatidylethanolamine, and arachidonic acid was incorporated mainly into phosphatidylethanolamine. Supplementation of the culture medium with particular fatty acids (myristic, palmitic, stearic, oleic, linoleic, alpha-linolenic, arachidonic, eicosapentaenoic or docosahexaenoic acid) led to enrichment of that fatty acid in both neutral lipids and phospholipids. This generated lymphocytes with phospholipids differing in saturated/unsaturated fatty acid ratio, degree of polyunsaturation, index of unsaturation and n - 6/n - 3 ratio. This method allowed the introduction into lymphocyte phospholipids of fatty acids not normally present (e.g. alpha-linolenic) or usually present in low proportions (eicosapentaenoic and docosahexaenoic). These three n - 3 polyunsaturated fatty acids replaced arachidonic acid in lymphocyte phospholipids. Fatty acid incorporation led to an alteration in lymphocyte membrane fluidity: palmitic and stearic acids decreased fluidity whereas the unsaturated fatty acids increased fluidity. It is proposed that the changes in lymphocyte phospholipid fatty acid composition and membrane fluidity brought about by culture in the presence of polyunsaturated fatty acids are responsible for the inhibition of lymphocyte functions caused by these fatty acids.
对大鼠淋巴结淋巴细胞中性脂质和磷脂部分的脂肪酸组成进行了表征。用T细胞丝裂原伴刀豆球蛋白A刺激大鼠淋巴细胞,导致中性脂质和磷脂的脂肪酸组成发生显著变化(硬脂酸、亚油酸和花生四烯酸的比例降低,油酸比例增加)。使用氮氧化物自旋标记电子顺磁共振测量膜流动性,在伴刀豆球蛋白A培养期间膜流动性增加。在无丝裂原的情况下培养淋巴细胞不影响脂肪酸组成或膜流动性。详细研究了棕榈酸、油酸、亚油酸和花生四烯酸的摄取和去向;每种脂肪酸都有时间依赖性地掺入所有脂质类别,但每种脂肪酸都有其特征性去向。棕榈酸和花生四烯酸主要掺入磷脂中,而油酸和亚油酸以相似比例掺入磷脂和三酰甘油中。油酸主要掺入磷脂酰胆碱,棕榈酸和亚油酸等量掺入磷脂酰胆碱和磷脂酰乙醇胺,花生四烯酸主要掺入磷脂酰乙醇胺。在培养基中添加特定脂肪酸(肉豆蔻酸、棕榈酸、硬脂酸、油酸、亚油酸、α-亚麻酸、花生四烯酸、二十碳五烯酸或二十二碳六烯酸)导致该脂肪酸在中性脂质和磷脂中均富集。这产生了饱和/不饱和脂肪酸比例、多不饱和程度、不饱和指数和n-6/n-3比例不同的淋巴细胞磷脂。该方法允许将通常不存在(如α-亚麻酸)或通常含量低(二十碳五烯酸和二十二碳六烯酸)的脂肪酸引入淋巴细胞磷脂中。这三种n-3多不饱和脂肪酸取代了淋巴细胞磷脂中的花生四烯酸。脂肪酸掺入导致淋巴细胞膜流动性改变:棕榈酸和硬脂酸降低流动性,而不饱和脂肪酸增加流动性。有人提出,在多不饱和脂肪酸存在下培养引起的淋巴细胞磷脂脂肪酸组成和膜流动性变化是这些脂肪酸抑制淋巴细胞功能的原因。