Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Eur Respir J ; 32(6): 1591-8, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18684846

ABSTRACT

The present study addressed the question whether ExoU, a Pseudomonas aeruginosa toxin with phospholipase A2 (PLA2) activity, may induce airway epithelial cells to overexpress tissue factor (TF) and exhibit a procoagulant phenotype. Cells from the human bronchial epithelial BEAS-2B line were infected with an ExoU-producing P. aeruginosa strain, pre-treated or not with the cytosolic PLA2 inhibitor methylarachidonyl fluorophosphate (MAFP), or with two ExoU-deficient mutants. Control noninfected and infected cells were assessed for the expression of: 1) TF mRNA by RT-PCR; 2) cell-associated TF by enzyme immunoassay and flow cytometry; 3) procoagulant activity by a colorimetric assay; and 4) microparticle-associated TF by flow cytometry. An enzyme immunoassay was also used to assess cell-associated TF in lung extracts from mice infected intratracheally with ExoU-producing and -deficient bacteria. Cells infected with the wild-type bacteria had higher levels of TF mRNA, cell-associated TF expression, procoagulant activity and released microparticle-associated TF than cells infected with the mutants. Bacterial treatment with MAFP significantly reduced the expression of TF by infected cells. Lung samples from mice infected with the wild-type bacteria exhibited higher levels of cell-associated TF and procoagulant activity. The present results demonstrate that ExoU may contribute to the pathogenesis of lung injury by inducing a tissue factor-dependent procoagulant activity in airway epithelial cells.


Subject(s)
Bacterial Proteins/physiology , Bronchi/microbiology , Coagulants/metabolism , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/metabolism , Animals , Arachidonic Acids/metabolism , Bacterial Proteins/metabolism , Bronchi/cytology , Cytosol/metabolism , Female , Humans , Mice , Models, Biological , Mutation , Organophosphonates/metabolism , Phospholipases A2/metabolism , Pseudomonas Infections/diagnosis , Thromboplastin/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...