Pseudomonas aeruginosa Exotoxin Pyocyanin Causes Cystic Fibrosis Airway Pathogenesis

被引:136
|
作者
Caldwell, Charles C. [2 ]
Chen, Yi [3 ]
Goetzmann, Holly S. [2 ]
Hao, Yonghua [1 ]
Borchers, Michael T. [4 ]
Hassett, Daniel J. [5 ]
Young, Lisa R. [3 ,6 ]
Mavrodi, Dmitri [7 ]
Thomashow, Linda [7 ]
Lau, Gee W. [1 ]
机构
[1] Univ Illinois, Dept Pathobiol, Urbana, IL 61802 USA
[2] Univ Cincinnati, Coll Med, Dept Surg, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Coll Med, Div Pulm & Crit Care Med, Cincinnati, OH USA
[4] Univ Cincinnati, Coll Med, Dept Environm Hlth, Cincinnati, OH 45267 USA
[5] Univ Cincinnati, Coll Med, Dept Mol Genet Biochem & Microbiol, Cincinnati, OH 45267 USA
[6] Cincinnati Childrens Hosp, Div Pulm Med, Cincinnati, OH USA
[7] Washington State Univ, Dept Plant Pathol, Agr Res Serv, Pullman, WA 99164 USA
来源
AMERICAN JOURNAL OF PATHOLOGY | 2009年 / 175卷 / 06期
关键词
GOBLET CELL HYPERPLASIA; MUCIN GENE-EXPRESSION; NF-KAPPA-B; EPITHELIAL-CELLS; PULMONARY-FIBROSIS; ENDOTHELIAL-CELLS; PHENAZINE-1-CARBOXYLIC ACID; NEUTROPHIL APOPTOSIS; OXIDATIVE STRESS; LUNG-DISEASE;
D O I
10.2353/ajpath.2009.090166
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The cystic fibrosis (CF) airway bacterial pathogen Pseudomonas aeruginosa secretes multiple virulence factors. Among these, the redox active exotoxin pyocyanin (PCN) is produced in concentrations up to 100 mu mol/L during infection of CF and other bronchiectatic airways. However, the contributions of PCN during infection of bronchiectatic airways are not appreciated. in this study, we demonstrate that PCN is critical for chronic infection in mouse airways and orchestrates adaptive immune responses that mediate lung damage. Wild-type FVBN mice chronically exposed to PCN developed goblet cell hyperplasia and metaplasia, airway fibrosis, and alveolar airspace destruction. Furthermore, after 12 weeks of exposure to PCN, mouse lungs down-regulated the expression of T helper (Th) type 1 cytokines and polarized toward a Th2 response. Cellular analyses indicated that chronic exposure to PCN profoundly increased the lung population of recruited macrophages, CD4(+) T cells. and neutrophils responsible for the secretion of these cytokines. PCN-mediated goblet cell hyperplasia and metaplasia required Th2 cytokine signaling through the Stat6 pathway. In summary, this study establishes that PCN is an important P. aeruginosa virulence factor capable of directly inducing pulmonary pathophysiology in mice, consistent with changes observed in CF and other bronchiectasis lungs. (Am J Pathol 2009, 175:2473-2488: DOI: 10.2353/ajpath.2009.090166))
引用
收藏
页码:2473 / 2488
页数:16
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