Schneemann M, Schoedon G, Linscheid P, Walter R, Blau N, Schaffner A
Department of Medicine, University of Zurich Medical School, University of Zurich Children's Hospital, Switzerland.
J Infect Dis. 1997 Jan;175(1):130-5. doi: 10.1093/infdis/175.1.130.
The search continues for high-output nitric oxide biosynthesis in human macrophages analogous to murine phagocytes. Recently, generation of nitrite in culture supernatants of human macrophages exposed to interferon-gamma and interleukin-4 (IFN-gamma/IL-4) was reported. The present study reproduces these findings and shows that L-arginine is not consumed and L-citrulline is not produced during this process. Furthermore, the biosynthesis of the obligatory cofactor tetrahydrobiopterin is not coinduced. These biochemical data provide support against a nitric oxide synthase contribution to nitrite accumulation. Nitrite was generated from nitrate salts even in cell-free media. Nitric oxide synthase activity but not nitrate reduction depended on molecular oxygen. Nitrite accumulation in experiments with IFN-gamma/IL-4 in human monocytes appears to be an in vitro artifact produced by nitrate-reducing activities contained in cytokine preparations.
目前仍在寻找人类巨噬细胞中类似于小鼠吞噬细胞的高产量一氧化氮生物合成过程。最近,有报道称,暴露于γ干扰素和白细胞介素-4(IFN-γ/IL-4)的人类巨噬细胞培养上清液中会生成亚硝酸盐。本研究重现了这些发现,并表明在此过程中L-精氨酸未被消耗,L-瓜氨酸也未产生。此外,必需辅助因子四氢生物蝶呤的生物合成也未被共同诱导。这些生化数据支持亚硝酸盐积累并非由一氧化氮合酶导致的观点。即使在无细胞培养基中,亚硝酸盐也是由硝酸盐产生的。一氧化氮合酶活性而非硝酸盐还原依赖于分子氧。在人类单核细胞中使用IFN-γ/IL-4进行的实验中,亚硝酸盐积累似乎是细胞因子制剂中所含的硝酸盐还原活性产生的一种体外假象。