von Bredow C, Birrer P, Griese M
Children's Clinic of Ludwig-Maximilians-University, Munich, Germany.
Eur Respir J. 2001 Apr;17(4):716-22. doi: 10.1183/09031936.01.17407160.
Inflammation and proteolytic processes play an important role in the progression of cystic fibrosis (CF) lung disease. The goal of this study was to describe bronchoalveolar lavage fluid (BALF) protein pattern of CF patients in comparison to controls and to assess if there is proteolytic degradation of surfactant protein A (SP-A), an important innate host defence component of the lungs. BALFs from 17 clinically stable CF patients and from eight healthy children were separated by two-dimensional gel electrophoresis. Silver staining was used to show BALF proteins and Western blotting to detect SP-A isoforms. In CF, BALF proteins of a low molecular weight < or = 20 kD were more abundant than in controls. Various proteins were seen in CF which were not present in controls and vice versa. Degradation of SP-A was present in 15 of 17 CF BALFs but in none of the controls, in contrast polymeric isoforms were seen in all controls and in four of 17 CF patients. Proteolytic damage to surfactant protein A and significant changes of normal bronchoalveolar lavage fluid proteins occur in lungs of cystic fibrosis patients. Identification of altered bronchoalveolar lavage fluid proteins may give new insights into pathogenic mechanisms and provide new targets for therapy.
炎症和蛋白水解过程在囊性纤维化(CF)肺部疾病的进展中起重要作用。本研究的目的是描述CF患者支气管肺泡灌洗液(BALF)的蛋白质图谱,并与对照组进行比较,同时评估肺的重要固有宿主防御成分表面活性蛋白A(SP-A)是否存在蛋白水解降解。对17例临床稳定的CF患者和8名健康儿童的BALF进行二维凝胶电泳分离。用银染显示BALF蛋白,用蛋白质印迹法检测SP-A异构体。在CF患者中,分子量≤20 kD的低分子量BALF蛋白比对照组更丰富。在CF患者中可见到对照组中不存在的多种蛋白质,反之亦然。17份CF BALF中有15份存在SP-A降解,而对照组中均未出现,相反,所有对照组以及17例CF患者中的4例均可见到聚合物异构体。囊性纤维化患者的肺中发生了表面活性蛋白A的蛋白水解损伤以及正常支气管肺泡灌洗液蛋白的显著变化。鉴定支气管肺泡灌洗液中改变的蛋白质可能为致病机制提供新的见解,并为治疗提供新的靶点。