Rockett K A, Brookes R, Udalova I, Vidal V, Hill A V, Kwiatkowski D
Molecular Infectious Disease Group, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom.
Infect Immun. 1998 Nov;66(11):5314-21. doi: 10.1128/IAI.66.11.5314-5321.1998.
Inducible synthesis of nitric oxide (NO) by macrophages is an important mechanism of the host defense against intracellular infection in mice, but the evidence for significant levels of inducible NO production by human macrophages is controversial. Here we report that the human promyelocytic cell line HL-60, when differentiated to a macrophage-like phenotype, acquires the ability to produce substantial amounts of NO on stimulation with LPS or 1, 25-dihydroxyvitamin D3 (1,25-D3) in the absence of activating factors such as gamma interferon. Expression of the inducible nitric oxide synthase (NOS2) was confirmed by sequencing of the reverse transcription-PCR product from stimulated HL-60 cells. Kinetic studies after lipopolysaccharide stimulation show that NOS2 mRNA levels rise within 3 to 6 h, that conversion of [14C]arginine to [14C]citrulline is maximal at 5 to 6 days, and that levels of reactive nitrogen intermediates stabilize at around 20 microM at 7 to 8 days. We find that 1,25-D3 acts to suppress the growth of Mycobacterium tuberculosis in these cells and that this effect is inhibited by NG-monomethyl-L-arginine, suggesting that vitamin D-induced NO production may play a role in the host defense against human tuberculosis.
巨噬细胞诱导性合成一氧化氮(NO)是小鼠宿主抵御细胞内感染的重要机制,但关于人类巨噬细胞可诱导产生大量NO的证据存在争议。在此我们报告,人类早幼粒细胞系HL-60分化为巨噬细胞样表型后,在无γ干扰素等激活因子的情况下,经脂多糖(LPS)或1,25-二羟维生素D3(1,25-D3)刺激,获得了产生大量NO的能力。通过对受刺激HL-60细胞逆转录-聚合酶链反应(RT-PCR)产物测序,证实了诱导型一氧化氮合酶(NOS2)的表达。脂多糖刺激后的动力学研究表明,NOS2 mRNA水平在3至6小时内升高,[14C]精氨酸向[14C]瓜氨酸的转化在5至6天时达到最大值,活性氮中间体水平在7至8天时稳定在约20微摩尔。我们发现1,25-D3可抑制这些细胞中结核分枝杆菌的生长,且该效应被NG-单甲基-L-精氨酸抑制,这表明维生素D诱导的NO产生可能在宿主抵御人类结核病中发挥作用。