John M, Au B T, Jose P J, Lim S, Saunders M, Barnes P J, Mitchell J A, Belvisi M G, Chung K F
Thoracic Medicine and Applied Pharmacology, National Heart and Lung Institute, Imperial College School of Medicine, London, United Kingdom.
Am J Respir Cell Mol Biol. 1998 Jan;18(1):84-90. doi: 10.1165/ajrcmb.18.1.2813.
Interleukin (IL)-8 is a C-X-C chemokine that potently chemoattracts and activates neutrophils. We determined whether IL-8 could be produced by human airway smooth muscle cells in culture and examined its regulation. TNF-alpha stimulated IL-8 mRNA expression and protein release in a time- and dose-dependent manner, whereas IFN-gamma alone had no effect. Both cytokines together did not induce greater IL-8 release compared to TNF-alpha alone. IL-1beta was more potent in inducing IL-8 release and, together with TNF-alpha, there was a synergistic augmentation of IL-8 release. IL-8 release induced by TNF-alpha and IFN-gamma was partly inhibited by the Th-2-derived cytokines IL-4, IL-10, and IL-13, as well as by dexamethasone. In addition to its contractile responses, airway smooth muscle cells have synthetic and secretory potential with the release of IL-8 and subsequent recruitment and activation of neutrophils in the airways. Release of IL-8 can be modulated by Th-2-derived cytokines and corticosteroids.
白细胞介素(IL)-8是一种C-X-C趋化因子,能有效地趋化和激活中性粒细胞。我们确定了培养的人气道平滑肌细胞是否能产生IL-8,并研究了其调控机制。肿瘤坏死因子-α(TNF-α)以时间和剂量依赖的方式刺激IL-8信使核糖核酸(mRNA)表达和蛋白质释放,而单独的γ干扰素(IFN-γ)则无作用。与单独使用TNF-α相比,两种细胞因子共同作用并未诱导更多的IL-8释放。白细胞介素-1β(IL-1β)在诱导IL-8释放方面更有效,并且与TNF-α一起,IL-8释放有协同增强作用。TNF-α和IFN-γ诱导的IL-8释放被Th-2衍生的细胞因子IL-4、IL-10和IL-13以及地塞米松部分抑制。除了其收缩反应外,气道平滑肌细胞具有合成和分泌潜能,可释放IL-8并随后在气道中募集和激活中性粒细胞。IL-8的释放可被Th-2衍生的细胞因子和皮质类固醇调节。