Pseudomonas aeruginosa pyocyanin inactivates lung epithelial vaculoar ATPase-dependent cystic fibrosis transmembrane conductance regulator expression and localization
Open Access
- 24 February 2006
- journal article
- Published by Hindawi Limited in Cellular Microbiology
- Vol. 8 (7), 1121-1133
- https://doi.org/10.1111/j.1462-5822.2006.00696.x
Abstract
Pseudomonas aeruginosa (PA) is a major pathogen causing morbidity and ultimately mortality in patients afflicted with cystic fibrosis (CF) lung disease. One important virulence factor, pyocyanin (PCN), is a blue, redox‐active compound that is secreted in such copious amounts by PA in the CF lungs that it determines the colour of expectorated sputum. In this study, we discovered that physiological concentrations of PCN inactivate the airway epithelial vacuolar ATPase, resulting in reduced expression and trafficking of the cystic fibrosis transmembrane conductance regulator in cultured lung and primary nasal epithelial cells. Our study supports the notion that PCN contributes significantly to the pathogenesis of CF and other bronchiectasis patients infected by PA.Keywords
This publication has 50 references indexed in Scilit:
- Pseudomonas aeruginosa Flagella Activate Airway Epithelial Cells through asialoGM1 and Toll-Like Receptor 2 as well as Toll-Like Receptor 5American Journal of Respiratory Cell and Molecular Biology, 2004
- Role of MDR1 and MRP1 in trophoblast cells, elucidated using retroviral gene transferAmerican Journal of Physiology-Cell Physiology, 2003
- Association of L-Type Calcium Channels with a Vacuolar H+-ATPase G2 SubunitBiochemical and Biophysical Research Communications, 2000
- Regulated trafficking of the CFTR chloride channelEuropean Journal of Cell Biology, 2000
- Interleukin-8 Production by Cystic Fibrosis Nasal Epithelial Cells after Tumor Necrosis Factor- α and Respiratory Syncytial Virus StimulationAmerican Journal of Respiratory Cell and Molecular Biology, 1998
- The Effect of Bacterial Toxins on Levels of Intracellular Adenosine Nucleotides and Human Ciliary Beat FrequencyPulmonary Pharmacology, 1996
- Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitiveNature, 1992
- Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutationNature, 1991
- Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2.Molecular and Cellular Biology, 1991
- Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisCell, 1990