Pang L, Knox A J
Division of Respiratory Medicine, City Hospital, University of Nottingham, Nottingham, UK.
FASEB J. 2001 Jan;15(1):261-269. doi: 10.1096/fj.00-0103com.
Eotaxin is a potent eosinophil chemoattractant that contributes to the eosinophilia seen in asthma and other allergic disorders. Recent studies have identified human airway smooth muscle (HASM) as a rich source of eotaxin, but the factors regulating its production are poorly understood. Here we describe for the first time that beta2-agonists can inhibit cytokine-induced eotaxin release. We found that TNF-alpha stimulated eotaxin release (assayed by ELISA) from HASM cells and that the release was partially inhibited by salbutamol and salmeterol. The effect of beta2-agonists was mimicked by forskolin and 8-bromo-cAMP and potentiated by the cAMP-dependent phosphodiesterase inhibitor rolipram, suggesting that it is cAMP dependent. We also found that the cAMP inhibition was likely at the transcription stage, although experiments with the PKA inhibitors H-89 and Rp-cAMP or the PKG inhibitor KT5823 suggested that none of these kinases was involved. Partial inhibition of eotaxin release was also seen with the corticosteroids dexamethasone and fluticasone. The combined use of beta2-agonists, rolipram, and steroids abolished TNF-alpha-induced eotaxin release. These results suggest that the combination of a beta2-agonist, PDE inhibitor, and a corticosteroid may have additive beneficial effects in the treatment of the eosinophilia associated with asthma and other allergic diseases.
嗜酸性粒细胞趋化因子是一种强效的嗜酸性粒细胞趋化剂,与哮喘及其他过敏性疾病中所见的嗜酸性粒细胞增多有关。最近的研究已确定人气道平滑肌(HASM)是嗜酸性粒细胞趋化因子的丰富来源,但调节其产生的因素却知之甚少。在此,我们首次描述β2-激动剂可抑制细胞因子诱导的嗜酸性粒细胞趋化因子释放。我们发现肿瘤坏死因子-α(TNF-α)刺激HASM细胞释放嗜酸性粒细胞趋化因子(通过酶联免疫吸附测定法检测),且沙丁胺醇和沙美特罗可部分抑制该释放。福斯可林和8-溴-环磷酸腺苷(8-bromo-cAMP)可模拟β2-激动剂的作用,而环磷酸腺苷依赖性磷酸二酯酶抑制剂咯利普兰可增强该作用,提示其作用依赖于环磷酸腺苷(cAMP)。我们还发现,cAMP抑制可能发生在转录阶段,尽管使用蛋白激酶A(PKA)抑制剂H-89和Rp-cAMP或蛋白激酶G(PKG)抑制剂KT5823进行的实验表明这些激酶均未参与。地塞米松和氟替卡松等皮质类固醇也可部分抑制嗜酸性粒细胞趋化因子释放。β2-激动剂、咯利普兰和类固醇联合使用可消除TNF-α诱导的嗜酸性粒细胞趋化因子释放。这些结果表明,β2-激动剂、磷酸二酯酶抑制剂和皮质类固醇联合使用可能在治疗与哮喘及其他过敏性疾病相关的嗜酸性粒细胞增多方面具有相加的有益作用。