Padgett E L, Pruett S B
Department of Biological Sciences, Mississippi State University, Mississippi 39762.
Immunology. 1995 Jan;84(1):135-41.
The role of reactive nitrogen intermediates (RNI) in the antimicrobial activities of neutrophils from various mammalian species is unclear. However, it has been reported that rodent neutrophils possess the inducible form of nitric oxide synthase and that inflammatory neutrophils from rats produce potentially antimicrobial levels of RNI. In the present study, neutrophils from humans, rats and mice were evaluated for production of nitrite, a stable end-product of RNI. Human neutrophil preparations (> 95% neutrophils) isolated from peripheral blood were stimulated for 2-24 hr with agents known to trigger the Ca(2+)-dependent constitutive nitric oxide synthase, or to stimulate synthesis of the inducible nitric oxide synthase. Superoxide dismutase was added to some cultures to decrease the levels of superoxide, a compound reported to react with RNI and yield products other than nitrite. Even though the cells were viable and responsive to stimuli, they did not produce nitrite concentrations indicative of antimicrobial potential. Preparations of inflammatory (casein-elicited) mouse neutrophils also failed to produce high concentrations of nitrite. Inflammatory rat neutrophils (2.5 x 10(6)/ml) produced nitrite concentrations of approximately 40 microM in 24-hr cultures, but plots of nitrite production versus cell number for neutrophil and macrophage preparations indicated that contaminating macrophages could account for all the nitrite production in the neutrophil preparations. Thus, neutrophils from rats, mice and humans seem comparable in their inability to produce high levels of nitrite in response to a variety of stimuli. This suggests that in most circumstances the constitutive nitric oxide synthase known to be present in these cells is limited to the production of low levels of nitric oxide for intercellular signalling. In addition, this raises questions about the presence or functional status of inducible nitric oxide synthase in rodent neutrophils.
活性氮中间体(RNI)在各种哺乳动物中性粒细胞抗菌活性中的作用尚不清楚。然而,据报道啮齿动物的中性粒细胞具有诱导型一氧化氮合酶,并且来自大鼠的炎性中性粒细胞可产生具有潜在抗菌水平的RNI。在本研究中,对来自人、大鼠和小鼠的中性粒细胞进行了亚硝酸盐生成评估,亚硝酸盐是RNI的一种稳定终产物。从外周血中分离的人中性粒细胞制剂(>95%为中性粒细胞)用已知可触发钙依赖性组成型一氧化氮合酶或刺激诱导型一氧化氮合酶合成的试剂刺激2 - 24小时。向一些培养物中添加超氧化物歧化酶以降低超氧化物水平,据报道超氧化物可与RNI反应并产生除亚硝酸盐以外的产物。尽管细胞存活且对刺激有反应,但它们并未产生表明具有抗菌潜力的亚硝酸盐浓度。炎性(酪蛋白诱导)小鼠中性粒细胞制剂也未能产生高浓度的亚硝酸盐。炎性大鼠中性粒细胞(2.5×10⁶/ml)在24小时培养物中产生的亚硝酸盐浓度约为40μM,但中性粒细胞和巨噬细胞制剂中亚硝酸盐生成量与细胞数量的关系图表明,污染的巨噬细胞可解释中性粒细胞制剂中所有的亚硝酸盐生成。因此,大鼠、小鼠和人的中性粒细胞在对各种刺激产生高水平亚硝酸盐的能力方面似乎相当。这表明在大多数情况下,已知存在于这些细胞中的组成型一氧化氮合酶仅限于产生低水平的一氧化氮用于细胞间信号传导。此外,这也引发了关于啮齿动物中性粒细胞中诱导型一氧化氮合酶的存在或功能状态的问题。