Bastian N R, Hibbs J B
Division of Infectious Diseases, University of Utah, School of Medicine, Salt Lake City 84132.
Curr Opin Immunol. 1994 Feb;6(1):131-9. doi: 10.1016/0952-7915(94)90044-2.
Research over the past year has revealed several interesting advances in the biosynthesis of the superoxide anion and nitric oxide. Highlights include the demonstration that the G protein Rac 2 is required for NADPH oxidase activation, the finding that nitric oxide is a feedback inhibitor of nitric oxide synthase isoforms, and the discovery that the continuous catalytic activity of the immune/inflammatory nitric oxide synthase is due to strong calmodulin binding, which is independent of elevated calcium levels. Interferon-gamma primes neutrophils and macrophages for both O2- and nitric oxide synthesis. However, NADPH oxidase and immune/inflammatory nitric oxide synthase are differentially regulated such that their activities are not simultaneously induced.
过去一年的研究揭示了超氧阴离子和一氧化氮生物合成方面的几项有趣进展。重点包括:证明G蛋白Rac 2是NADPH氧化酶激活所必需的;发现一氧化氮是一氧化氮合酶同工型的反馈抑制剂;以及发现免疫/炎症性一氧化氮合酶的持续催化活性归因于与钙调蛋白的强结合,这与钙水平升高无关。干扰素-γ使中性粒细胞和巨噬细胞对O2-和一氧化氮的合成做好准备。然而,NADPH氧化酶和免疫/炎症性一氧化氮合酶受到不同调节,因此它们的活性不会同时被诱导。