细菌脂多糖刺激人中性粒细胞表达前列腺素G/H合成酶2基因

Mary B. Fasano , Jon D. Wells, Charles E. McCall
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引用次数: 25

摘要

人血液中性粒细胞(PMN)在体外用多种炎症激动剂刺激时,从细胞磷脂中迅速释放花生四烯酸(AA)。然后,游离AA通过5 ' -脂氧合酶代谢产生生物活性介质,如白三烯b4和5-羟基二糖四烯酸酯。花生四烯酸也可以通过环加氧酶或前列腺素G/H合成酶(PGHS)途径代谢,形成前列腺素和凝血素。我们在这里表明,当受到细菌脂多糖(LPS)刺激时,人血液PMN表达PGHS 2基因。PGHS 2 mRNA在LPS刺激后30分钟内升高,5小时后可检测到PGHS 2免疫反应蛋白。尽管PMN中可检测到PGHS 1 mRNA,但在静息或LPS刺激的细胞中均未观察到免疫反应蛋白。在LPS刺激和pghs2表达后,PMN增加前列腺素E2的分泌。PMN的这种表型变化可能是调节炎症的重要机制。
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Human Neutrophils Express the Prostaglandin G/H Synthase 2 Gene When Stimulated with Bacterial Lipopolysaccharide

Human blood neutrophils (PMN) rapidly release arachidonic acid (AA) from cellular phospholipids when stimulatedin vitrowith a variety of inflammatory agonists. Free AA is then metabolized via 5′-lipoxygenase to produce bioactive mediators such as leukotriene B4and 5-hydroxyeicosatetraenoate. Arachidonic acid can also be metabolized via the cyclooxygenase or prostaglandin G/H synthase (PGHS) pathway to form prostaglandins and thromboxane. We show here that human blood PMN express the PGHS 2 gene when stimulated with bacterial lipopolysaccharide (LPS). PGHS 2 mRNA increases within 30 min after LPS stimulation and PGHS 2 immunoreactive protein is detectable by 5 h. Although PGHS 1 mRNA is detectable in PMN, no immunoreactive protein is observed in either resting or LPS-stimulated cells. Following stimulation with LPS and expression of PGHS 2, PMN increase secretion of prostaglandin E2. This phenotypic change in PMN could be an important mechanism for regulating inflammation.

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