Hamilton L M, Puddicombe S M, Dearman R J, Kimber I, Sandström T, Wallin A, Howarth P H, Holgate S T, Wilson S J, Davies D E
The Brooke Laboratories, Mailpoint 888, Southampton General Hospital, Southampton, SO16 6YD, UK.
Eur Respir J. 2005 Jun;25(6):978-85. doi: 10.1183/09031936.05.00098604.
A disease-related, corticosteroid-insensitive increase in the expression of epidermal growth factor (EGF) receptor (EGFR) tyrosine kinase in asthmatic bronchial epithelium has been shown previously by the current authors. To determine whether this is associated with enhanced intracellular signalling, the aim of this study was to evaluate epithelial tyrosine phosphorylation. Bronchial biopsies were analysed for the presence of phosphotyrosine by immunohistochemistry. Bronchial epithelial cells were exposed to EGF, hydrogen peroxide or tumour necrosis factor-alpha in vitro for measurement of tyrosine phosphorylated signalling intermediates and interleukin (IL)-8 release. Phosphotyrosine was increased significantly in the epithelium of severe asthmatics when compared with controls or mild asthmatics; however, in mild asthma, phosphotyrosine levels were significantly decreased when compared with controls. There was no significant difference between phosphotyrosine levels before or after 8 weeks of treatment with budesonide. Stimulation of bronchial epithelial cells resulted in tyrosine phosphorylation of several proteins, including EGFR, Shc and p42/p44 mitogen-activated protein kinase. In the presence of salbutamol, a transient partial suppression of EGFR phosphorylation occurred, whereas dexamethasone was without effect. Neither salbutamol nor dexamethasone inhibited EGF-stimulated IL-8 release. These data indicate that regulation of protein tyrosine kinase activity is abnormal in severe asthma. The epidermal growth factor receptor and/or other tyrosine kinase pathways may contribute to persistent, corticosteroid-unresponsive inflammation in severe asthma.
本文作者之前已表明,哮喘患者支气管上皮中表皮生长因子(EGF)受体(EGFR)酪氨酸激酶的表达出现与疾病相关的、对皮质类固醇不敏感的增加。为了确定这是否与细胞内信号增强有关,本研究的目的是评估上皮酪氨酸磷酸化。通过免疫组织化学分析支气管活检组织中磷酸酪氨酸的存在情况。在体外将支气管上皮细胞暴露于EGF、过氧化氢或肿瘤坏死因子-α,以测量酪氨酸磷酸化信号中间体和白细胞介素(IL)-8的释放。与对照组或轻度哮喘患者相比,重度哮喘患者上皮中的磷酸酪氨酸显著增加;然而,与对照组相比,轻度哮喘患者的磷酸酪氨酸水平显著降低。布地奈德治疗8周前后,磷酸酪氨酸水平无显著差异。刺激支气管上皮细胞导致几种蛋白质的酪氨酸磷酸化,包括EGFR、Shc和p42/p44丝裂原活化蛋白激酶。在沙丁胺醇存在的情况下,EGFR磷酸化出现短暂的部分抑制,而地塞米松则无作用。沙丁胺醇和地塞米松均未抑制EGF刺激的IL-8释放。这些数据表明,重度哮喘中蛋白质酪氨酸激酶活性的调节异常。表皮生长因子受体和/或其他酪氨酸激酶途径可能导致重度哮喘中持续的、对皮质类固醇无反应的炎症。