Garrelds I M, van Hal P T, Haakmat R C, Hoogsteden H C, Saxena P R, Zijlstra F J
Institute of Pharmacology, Faculty of Medicine, Erasmus University Rotterdam, The Netherlands.
Mediators Inflamm. 1999;8(4-5):229-35. doi: 10.1080/09629359990397.
In the present study the human monoblast cell line U937 has been used as a model to study the function of human mononuclear phagocytes in asthma. The kinetics of the production of eicosanoids and cytokines, which are thought to play a role in the pathogenesis of asthma, were studied. In addition, the effects of glucocorticosteroids were investigated, as these drugs are of great importance for the treatment of asthmatic patients. After stimulation with phorbol-12 myristate acetate (PMA) for 24 h, U937 cells were cultured in the absence or presence of lipopolysaccharide (LPS: 1 and 5 microg ml(-1)) and glucocorticosteroids (budesonide, fluticasone propionate and prednisolone: 10(-11), 10(-9) and 10(-7) M) for 96 h. The production of interleukin-1beta (IL-1beta), interleukin-6 (IL-6), prostaglandin E2 (PGE2) and thromboxane B2 (TxB2) gradually increased in time after stimulation with LPS, whereas the transient production of tumor necrosis factor alpha (TNF-alpha) reached its maximum between 6 and 12 h. Interferon-gamma (IFN-gamma), interleukin-10 (IL-10) and leukotriene B4 (LTB4) were not detectable. All three glucocorticosteroids (budesonide, fluticasone propionate and prednisolone) completely inhibited the production of both eicosanoids and cytokines. The production of eicosanoids was more sensitive to these glucocorticoids than the production of cytokines. The observed differences in the kinetics of the production of eicosanoids and cytokines stress the importance of time course experiments in studies on the effect of drugs on mononuclear cells.
在本研究中,人单核细胞系U937被用作模型,以研究人单核吞噬细胞在哮喘中的功能。研究了被认为在哮喘发病机制中起作用的类花生酸和细胞因子的产生动力学。此外,还研究了糖皮质激素的作用,因为这些药物对哮喘患者的治疗非常重要。在用佛波酯-12-肉豆蔻酸酯-13-乙酸酯(PMA)刺激24小时后,将U937细胞在不存在或存在脂多糖(LPS:1和5微克/毫升)和糖皮质激素(布地奈德、丙酸氟替卡松和泼尼松龙:10^(-11)、10^(-9)和10^(-7)摩尔)的情况下培养96小时。在用LPS刺激后,白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、前列腺素E2(PGE2)和血栓素B2(TxB2)的产生随时间逐渐增加,而肿瘤坏死因子α(TNF-α)的瞬时产生在6至12小时之间达到最大值。未检测到干扰素-γ(IFN-γ)、白细胞介素-10(IL-10)和白三烯B4(LTB4)。所有三种糖皮质激素(布地奈德、丙酸氟替卡松和泼尼松龙)均完全抑制类花生酸和细胞因子的产生。类花生酸的产生比细胞因子的产生对这些糖皮质激素更敏感。观察到的类花生酸和细胞因子产生动力学的差异强调了在研究药物对单核细胞作用时进行时间进程实验的重要性。