Henderson S A, Lee P H, Aeberhard E E, Adams J W, Ignarro L J, Murphy W J, Sherman M P
Department of Physiological Science, UCLA 90024.
J Biol Chem. 1994 Oct 14;269(41):25239-42.
Since early growth response-1 (Egr-1) is required for macrophage differentiation and nitric oxide (NO) is immunosuppressive, we hypothesized that NO would reduce Egr-1 expression in rat lung macrophages. The inflammatory stimuli interferon-gamma and lipopolysaccharide induced an early, transient increase in Egr-1 mRNA (> 5-fold at 2 h) and a sustained, high level of inducible NO synthase mRNA (> 100-fold from 4 to 24 h). The NO metabolites nitrite and nitrate rose > 10-fold in medium from stimulated versus unstimulated cells over 24 h. Concomitant with elevated nitrogen oxides, Egr-1 mRNA levels declined to 80% below unstimulated cells at 24 h. This decline was blocked by an inhibitor of NO production, NG-monomethyl-L-arginine. Further, the NO donor S-nitroso-N-acetylpenicillamine inhibited Egr-1 expression in a dose-dependent manner, producing complete inhibition at 0.5 mM. The effect of S-nitroso-N-acetylpenicillamine was not due to reduced macrophage viability. We conclude that Egr-1 induction precedes inducible NO synthase induction in stimulated rat macrophages and that subsequent NO production reduces macrophage expression of Egr-1. We propose that this mechanism is used to regulate macrophage differentiation in human immunodeficiency virus infection and other inflammatory states.
由于早期生长反应因子-1(Egr-1)是巨噬细胞分化所必需的,且一氧化氮(NO)具有免疫抑制作用,我们推测NO会降低大鼠肺巨噬细胞中Egr-1的表达。炎性刺激物γ干扰素和脂多糖诱导Egr-1 mRNA早期短暂增加(2小时时增加超过5倍)以及诱导型一氧化氮合酶mRNA持续高水平表达(4至24小时增加超过100倍)。在24小时内,受刺激细胞培养基中的NO代谢产物亚硝酸盐和硝酸盐比未受刺激细胞升高了10倍以上。与氮氧化物升高相伴,Egr-1 mRNA水平在24小时时降至未受刺激细胞的80%以下。这种下降被NO生成抑制剂NG-单甲基-L-精氨酸阻断。此外,NO供体S-亚硝基-N-乙酰青霉胺以剂量依赖方式抑制Egr-1表达,在0.5 mM时产生完全抑制。S-亚硝基-N-乙酰青霉胺的作用并非由于巨噬细胞活力降低。我们得出结论,在受刺激的大鼠巨噬细胞中,Egr-1的诱导先于诱导型一氧化氮合酶的诱导,随后产生的NO降低了巨噬细胞中Egr-1的表达。我们提出,这种机制用于调节人类免疫缺陷病毒感染和其他炎症状态下的巨噬细胞分化。