Palazzolo-Ballance Amy M, Suquet Christine, Hurst James K
Department of Chemistry, Washington State University, Pullman, Washington 99164-4630, USA.
Biochemistry. 2007 Jun 26;46(25):7536-48. doi: 10.1021/bi700123s. Epub 2007 May 27.
Two transformed murine macrophage cell lines (RAW 264.7 ATCC TIB-71 and CRL-2278) were examined for oxidant production at various times following activation by using a set of fluorescence and ESR-active probes. Stimulation with a soluble agonist or activation with bacterial lipopolysaccharide plus gamma-interferon caused only very small initial increases in O2 consumption above basal rates; however, at 2-4 h post-activation, respiration increased to 2-3-fold and remained at these elevated levels over the subsequent lifetime of the cell (20-30 h). Oxidation reactions were confined primarily within the cell, as was demonstrated by using phagocytosable dichlorodihydrofluorescein-conjugated latex beads and cyclic hydroxylamines with differing membrane permeabilities. From the intrinsic reactivities of these probes and the time course of their oxidations, one infers the induction of apparent peroxidase activity beginning at approximately 2 h post-activation coinciding with the increase in overall respiratory rate; this acquired capability was accompanied by accumulation of a stable horseradish peroxidase-reactive oxidant, presumably H2O2, in the extracellular medium. Nitrite ion rapidly accumulated in the extracellular medium over a period of 5-8 h post-activation in both cell lines, indicating the presence of active nitric oxide synthase (iNOS) during that period. Prostaglandin endoperoxide H synthase (COX-2) activity was detected at 15-20 h post-activation by the use of a sensitive peroxide assay in conjunction with a COX-2 specific inhibitor (DuP-697). Superoxide formation was detected by reaction with hydroethidine within the first hour following activation, but not thereafter. Consistent with the absence of significant respiratory stimulation, the amount of O2*- formed was very small; comparative reactions of cyclic hydroxylamine probes indicated that virtually none of the O2*- was discharged into the external medium. Myeloperoxidase (MPO) activity was probed at various times post-activation by using fluorescein-conjugated polyacrylamide beads, which efficiently trap MPO-generated HOCl in neutrophils to give stable chlorofluorescein products. However, chlorination of the dye was not detected under any conditions in RAW cells, virtually precluding MPO involvement in their intracellular reactions. This same probe was used to determine changes in intraphagosomal pH, which increased slowly from approximately 6.5 to approximately 8.2 over a 20 h post-phagocytosis period. The cumulative data suggest that activation is followed by sequential induction of an endogenous peroxidase, iNOS, and COX-2, with NADPH oxidase-derived O2*- playing a minimal role in the direct generation of intracellular oxidants. To account for reported observations of intracellular tyrosine nitration late in the life cycles of macrophages, we propose a novel mechanism wherein iNOS-generated NO2- is used by COX-2 to produce NO2* as a terminal microbicidal oxidant and nitrating agent.
使用一组荧光和电子自旋共振(ESR)活性探针,检测了两种转化的小鼠巨噬细胞系(RAW 264.7 ATCC TIB - 71和CRL - 2278)在激活后不同时间的氧化剂产生情况。用可溶性激动剂刺激或用细菌脂多糖加γ - 干扰素激活,仅使初始耗氧量比基础速率略有增加;然而,在激活后2 - 4小时,呼吸作用增加到2 - 3倍,并在细胞的后续存活期(20 - 30小时)内维持在这些升高的水平。氧化反应主要局限于细胞内,这通过使用可吞噬的二氯二氢荧光素共轭乳胶珠和具有不同膜通透性的环状羟胺得以证明。根据这些探针的固有反应性及其氧化的时间进程,可以推断在激活后约2小时开始诱导明显的过氧化物酶活性,这与总体呼吸速率的增加同时发生;这种获得的能力伴随着细胞外培养基中稳定的辣根过氧化物酶反应性氧化剂(可能是H2O2)的积累。在激活后5 - 8小时内,两种细胞系的细胞外培养基中亚硝酸根离子迅速积累,表明在此期间存在活性一氧化氮合酶(iNOS)。通过使用灵敏的过氧化物测定法结合COX - 2特异性抑制剂(DuP - 697),在激活后15 - 20小时检测到前列腺素内过氧化物H合酶(COX - 2)活性。在激活后的第一小时内通过与氢乙锭反应检测到超氧阴离子的形成,但此后未检测到。与缺乏显著的呼吸刺激一致,形成的O2*-量非常小;环状羟胺探针的比较反应表明,几乎没有O2*-释放到外部培养基中。在激活后的不同时间,使用荧光素共轭的聚丙烯酰胺珠检测髓过氧化物酶(MPO)活性,该珠子可有效捕获中性粒细胞中MPO产生的HOCl以产生稳定的氯荧光素产物。然而,在RAW细胞的任何条件下均未检测到染料的氯化,实际上排除了MPO参与其细胞内反应。使用相同的探针来确定吞噬体内pH的变化,在吞噬后20小时内,pH从约6.5缓慢增加到约8.2。累积数据表明,激活后依次诱导内源性过氧化物酶、iNOS和COX - 2,而NADPH氧化酶衍生的O2*-在细胞内氧化剂的直接产生中起最小作用。为了解释巨噬细胞生命周期后期细胞内酪氨酸硝化的报道观察结果,我们提出了一种新机制,其中iNOS产生的NO2-被COX - 2用于产生NO2*作为终末杀菌氧化剂和硝化剂。