Doran O, Stahl J, Cook E, Buckner C K, Graziano F M
Department of Medicine, University of Wisconsin, Madison 53706.
Inflammation. 1994 Feb;18(1):89-97. doi: 10.1007/BF01534601.
Guinea pig lung mast cells can be isolated and purified to high purity. This has given us the opportunity to study in greater detail mediator release from these cells. Both immunologic (ovalbumin sensitized) and nonimmunologic (calcium ionophore, CaI) stimuli caused a dose-dependent release of histamine and pLT from monodispersed lung cells and highly purified lung mast cells. Examination of the time release curve for pLT revealed a 5-min lag in the release of this mediator and a peak release at 60 min after challenge with antigen. Verification of pLT release was obtained by use of the 5-lipoxygenase inhibitor A64077 (Zileuton). Pretreatment of lung mast cells with the 5-lipoxygenase inhibitor prevented release of pLT by either antigen or CaI but had no appreciable effect on histamine release (HR). The pulmonary mast cell appears to be an important contributor to pLT release in the guinea pig lung.
豚鼠肺肥大细胞可以被分离并纯化至高纯度。这使我们有机会更详细地研究这些细胞的介质释放。免疫(卵清蛋白致敏)和非免疫(钙离子载体,CaI)刺激均导致组胺和pLT从单分散肺细胞和高度纯化的肺肥大细胞中呈剂量依赖性释放。对pLT的时间释放曲线的检查显示,该介质的释放在5分钟时有一个延迟,在用抗原攻击后60分钟时释放达到峰值。通过使用5-脂氧合酶抑制剂A64077(齐留通)来验证pLT的释放。用5-脂氧合酶抑制剂对肺肥大细胞进行预处理可防止抗原或CaI诱导的pLT释放,但对组胺释放(HR)没有明显影响。肺肥大细胞似乎是豚鼠肺中pLT释放的一个重要贡献者。