Lefkowith J B, Jakschik B A, Stahl P, Needleman P
J Biol Chem. 1987 May 15;262(14):6668-75.
Essential fatty acid (EFA) deficiency has been shown to protect against the glomerulonephritis in a murine model of systemic lupus erythematosus. Since macrophages are an important cellular constituent of the inflammatory lesion, the effects of EFA deficiency on the eicosanoid metabolism and function of these cells were determined. EFA-deficient macrophages exhibited a depletion of phospholipid arachidonate and an accumulation of 20:3(n-9); phosphatidylinositol was the phospholipid most affected. When these macrophages were stimulated with unopsonized zymosan, they produced markedly less leukotriene C4 and B4 than control macrophages. EFA-deficient macrophages also synthesized leukotriene C3 from endogenous 20:3(n-9). No leukotriene B3 was detected. In contrast to the effects on leukotriene production, prostaglandin and thromboxane production were only minimally affected by EFA deficiency. When challenged with zymosan, EFA-deficient macrophages released less arachidonate relative to control macrophages and released half again as much 20:3(n-9) as arachidonate. Release of arachidonate from phosphatidylcholine in the EFA-deficient cells was highly selective for arachidonate; however, release of arachidonate from phosphatidylinositol was depressed relative to control and was not selective. Incubation of macrophages with exogenous arachidonate and 20:3(n-9) established that 20:3(n-9) decreased leukotriene C4 and B4 synthesis from arachidonate but did not affect prostaglandin production. To determine the functional effects of the deficiency state, receptor-mediated pinocytosis and phagocytosis were also examined in EFA-deficient cells. EFA-deficient macrophages exhibited a marked reduction in receptor-mediated pinocytosis. Phagocytosis, however, was unaffected by the deficiency state. These effects on macrophage eicosanoid metabolism and function may comprise a significant component of the anti-inflammatory effect of EFA deficiency.
在系统性红斑狼疮的小鼠模型中,已证明必需脂肪酸(EFA)缺乏可预防肾小球肾炎。由于巨噬细胞是炎症病变的重要细胞成分,因此确定了EFA缺乏对这些细胞类花生酸代谢和功能的影响。EFA缺乏的巨噬细胞表现出磷脂花生四烯酸的消耗和20:3(n-9)的积累;磷脂酰肌醇是受影响最大的磷脂。当用未调理的酵母聚糖刺激这些巨噬细胞时,它们产生的白三烯C4和B4明显少于对照巨噬细胞。EFA缺乏的巨噬细胞还从内源性20:3(n-9)合成白三烯C3。未检测到白三烯B3。与对白三烯产生的影响相反,EFA缺乏对前列腺素和血栓素产生的影响很小。当受到酵母聚糖攻击时,EFA缺乏的巨噬细胞相对于对照巨噬细胞释放的花生四烯酸较少,并且释放的20:3(n-9)是花生四烯酸的1.5倍。EFA缺乏细胞中花生四烯酸从磷脂酰胆碱的释放对花生四烯酸具有高度选择性;然而,相对于对照,花生四烯酸从磷脂酰肌醇的释放受到抑制且没有选择性。用外源性花生四烯酸和20:3(n-9)孵育巨噬细胞表明,20:3(n-9)减少了花生四烯酸合成白三烯C4和B4,但不影响前列腺素的产生。为了确定缺乏状态的功能影响,还在EFA缺乏的细胞中检查了受体介导的胞饮作用和吞噬作用。EFA缺乏的巨噬细胞表现出受体介导的胞饮作用明显降低。然而,吞噬作用不受缺乏状态的影响。这些对巨噬细胞类花生酸代谢和功能的影响可能是EFA缺乏抗炎作用的重要组成部分。