Spagnuolo P J, Ellner J J, Hassid A, Dunn M J
J Clin Invest. 1980 Sep;66(3):406-14. doi: 10.1172/JCI109870.
We examined the role of prostaglandins and thromboxanes as mediators of plasma-dependent increased polymorphonuclear leukocyte adhesiveness induced by Escherichia coli lipopolysaccharide. The cyclo-oxygenase inhibitors-indomethacin and d,l-6-chloro-alpha-methyl-carbozole-2-acetic acid (R020-5720)-reduced lipopolysaccharide-induced adherence of polymorphonuclear leukocytes by 74 and 62%, respectively. In addition, inhibitors of thromboxane synthetase-imidazole, 9,11-azoprosta-5,13-dienoic acid, and 1-benzylimidazole-suppressed the stimulation of adherence by 31, 66, and 83%, respectively. Exogenous prostaglandins E(1), E(2), and F(2)alpha did not increase polymorphonuclear leukocyte adherence, nor were they detected in significant quantities in supernates of polymorphonuclear leukocytes exposed to lipopolysaccharide. However, inhibitors of both cyclo-oxygenase and thromboxane synthetase reduced increases in adherence induced by arachidonic acid (10 mug/ml), suggesting that lipopolysaccharide-mediated increases in adherence were due to an arachidonic acid product other than prostaglandin E(2) or F(2)alpha. 8,11,14-Eicosatrienoic acid, a precursor of monoenoic prostaglandins, did not enhance polymorphonuclear leukocyte adhesiveness. We next demonstrated lipopolysaccharide-stimulated generation, by polymorphonuclear leukocytes, of a labile, low molecular weight, dialyzable substance capable of enhancing the adherence of unstimulated leukocytes. In parallel experiments, a 10-fold increase in immunoreactive thromboxane B(2) over basal levels was detected after exposure of leukocytes to lipopolysaccharide. The inhibition of lipopolysaccharide enhancement of adherence by specific rabbit antibodies to thromboxane B(2) strongly supported a primary role for thromboxane A(2) as the mediator of the observed increases in adherence. Lipopolysaccharide-stimulated purified platelets did not increase leukocyte adherence, whereas thrombin-stimulated platelets did increase adherence. These studies suggest that lipopolysaccharide stimulates polymorphonuclear leukocytes to produce thromboxane A(2), which enhances their adhesiveness to nylon.
我们研究了前列腺素和血栓素作为大肠杆菌脂多糖诱导的血浆依赖性多形核白细胞黏附性增加的介质的作用。环氧化酶抑制剂——吲哚美辛和d,l-6-氯-α-甲基-咔唑-2-乙酸(R020-5720)——分别使脂多糖诱导的多形核白细胞黏附减少了74%和62%。此外,血栓素合成酶抑制剂——咪唑、9,11-氮杂前列腺素-5,13-二烯酸和1-苄基咪唑——分别使黏附刺激减少了31%、66%和83%。外源性前列腺素E(1)、E(2)和F(2)α并未增加多形核白细胞黏附性,在暴露于脂多糖的多形核白细胞的上清液中也未检测到大量的这些物质。然而,环氧化酶和血栓素合成酶的抑制剂均减少了花生四烯酸(10微克/毫升)诱导的黏附增加,这表明脂多糖介导的黏附增加是由于除前列腺素E(2)或F(2)α之外的花生四烯酸产物所致。8,11,14-二十碳三烯酸,一种单烯前列腺素的前体,并未增强多形核白细胞黏附性。接下来,我们证明了脂多糖刺激多形核白细胞产生一种不稳定的、低分子量的、可透析的物质,该物质能够增强未刺激白细胞的黏附性。在平行实验中,白细胞暴露于脂多糖后,免疫反应性血栓素B(2)比基础水平增加了10倍。用针对血栓素B(2)的特异性兔抗体抑制脂多糖增强的黏附性,有力地支持了血栓素A(2)作为观察到的黏附增加的介质的主要作用。脂多糖刺激的纯化血小板并未增加白细胞黏附性,而凝血酶刺激的血小板确实增加了黏附性。这些研究表明,脂多糖刺激多形核白细胞产生血栓素A(2),从而增强其对尼龙的黏附性。