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Macrophage synthesis of nitrite, nitrate, and N-nitrosamines: precursors and role of the respiratory burst.

机译:亚硝酸盐,硝酸盐和N-亚硝胺的巨噬细胞合成:呼吸爆发的前体和作用。

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摘要

The macrophage cell line RAW 264.7 when activated with Escherichia coli lipopolysaccharide and interferon-gamma synthesized nitrite (NO3-) and nitrate (NO3-). Medium change after the activation showed that L-arginine was the only amino acid essential for this synthesis. D-Arginine would not substitute for L-arginine. Other analogues that could replace L-arginine were L-homoarginine, L-arginine methyl ester, L-arginamide, and the peptide L-arginyl-L-aspartate. L-Argininic acid, L-agmatine, L-ornithine, urea, L-citrulline, and ammonia were among the nonprecursors, while L-canavanine inhibited this L-arginine-derived NO2-/NO3- synthesis. When morpholine was added to the culture medium of the activated RAW 264.7 macrophages, N-nitrosation took place, generating N-nitrosomorpholine. GC/MS experiments using L-[guanido-15N2]arginine established that the NO2-/NO3- and the nitrosyl group of N-nitrosomorpholine were derived exclusively from one or both of the terminal guanido nitrogens of arginine. Chromatographic analysis showed that the other product of the L-arginine synthesis of NO2-/NO3- was L-citrulline. The role of the respiratory burst in NO2-/NO3- synthesis was examined using the macrophage cell lines J774.16 and J774 C3C. Both cell lines synthesized similar amounts of NO2-/NO3-. However, J774 C3C cells do not produce superoxide and hence do not exhibit the respiratory burst. Additional experiments also ruled out the involvement of the respiratory burst in NO2-/NO3- synthesis.
机译:当被大肠杆菌脂多糖和干扰素-γ合成的亚硝酸盐(NO3-)和硝酸盐(NO3-)激活时,巨噬细胞系RAW 264.7。活化后的培养基变化表明,L-精氨酸是该合成必需的唯一氨基酸。 D-精氨酸不能代替L-精氨酸。可以代替L-精氨酸的其他类似物是L-高精氨酸,L-精氨酸甲酯,L-精氨酰胺和肽L-精氨酸-L-天冬氨酸。 L-精氨酸,L-胍丁胺,L-鸟氨酸,尿素,L-瓜氨酸和氨属于非前体,而L-黄花氨酸抑制这种L-精氨酸衍生的NO2- / NO3-的合成。当将吗啉加入活化的RAW 264.7巨噬细胞的培养基中时,发生N-亚硝化,生成N-亚硝基吗啉。使用L- [胍基-15N2]精氨酸的GC / MS实验确定,N2-亚硝基吗啉的NO2- / NO3-和亚硝酰基仅来自精氨酸的一个或两个末端胍基氮。色谱分析表明,L 2-精氨酸合成的NO 2-/ NO 3-的另一个产物是L-瓜氨酸。使用巨噬细胞系J774.16和J774 C3C检查了呼吸爆发在NO2- / NO3-合成中的作用。两种细胞系均合成了相似量的NO2- / NO3-。但是,J774 C3C细胞不会产生超氧化物,因此不会表现出呼吸爆发。另外的实验也排除了呼吸爆发参与NO2- / NO3-合成。

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