Dohrman A, Miyata S, Gallup M, Li J D, Chapelin C, Coste A, Escudier E, Nadel J, Basbaum C
Department of Anatomy, University of California San Francisco, San Francisco CA 94143, USA.
Biochim Biophys Acta. 1998 Apr 28;1406(3):251-9. doi: 10.1016/s0925-4439(98)00010-6.
Bacterial infection of the lung is associated with mucin overproduction. In partial explanation of this phenomenon, we recently reported that supernatant from the Gram-negative organism Pseudomonas (P.) aeruginosa contained an activity that upregulated transcription of the MUC 2 mucin gene [J.-D. Li, A. Dohrman, M. Gallup, S. Miyata, J. Gum, Y. Kim, J. Nadel, A. Prince, C. Basbaum, Transcriptional activation of mucin by P. aeruginosa lipopolysaccharide in the pathogenesis of cystic fibrosis lung disease, Proc. Natl. Acad. Sci. U.S.A., 94 (1997) 967-972]. The purpose of the present study was to determine whether mucin genes other than MUC 2 are so regulated and whether Gram-positive organisms also contain mucin stimulatory activity. Results from in situ hybridization and RNase protection assays showed that P. aeruginosa upregulates MUC 5AC as well as MUC 2 in both bronchial explants and cultured airway epithelial cells. The upregulation of both genes by P. aeruginosa can be mimicked by lipopolysaccharide (LPS) and can be blocked by the tyrosine kinase inhibitor genistein. In addition, both genes are upregulated by a variety of Gram-positive as well as Gram-negative organisms showing the same rank order of potency. These data indicate the existence of a general mechanism by which epithelial cells respond to the presence of bacteria by increasing mucin synthesis.
肺部细菌感染与粘蛋白过度产生有关。作为对这一现象的部分解释,我们最近报道,革兰氏阴性菌铜绿假单胞菌(P. aeruginosa)的上清液含有一种能上调MUC 2粘蛋白基因转录的活性物质[J.-D. 李、A. 多尔曼、M. 盖洛普、S. 宫田、J. 古姆、Y. 金、J. 纳德尔、A. 普林斯、C. 巴斯鲍姆,铜绿假单胞菌脂多糖在囊性纤维化肺病发病机制中对粘蛋白的转录激活,《美国国家科学院院刊》,94 (1997) 967 - 972]。本研究的目的是确定除MUC 2之外的其他粘蛋白基因是否也受到如此调控,以及革兰氏阳性菌是否也含有粘蛋白刺激活性。原位杂交和核糖核酸酶保护分析结果表明,铜绿假单胞菌在支气管外植体和培养的气道上皮细胞中均上调MUC 5AC以及MUC 2。铜绿假单胞菌对这两个基因的上调作用可被脂多糖(LPS)模拟,并可被酪氨酸激酶抑制剂染料木黄酮阻断。此外,多种革兰氏阳性菌和革兰氏阴性菌均能上调这两个基因,且呈现相同的效力等级顺序。这些数据表明存在一种普遍机制,上皮细胞通过该机制对细菌的存在做出反应,增加粘蛋白合成。