[HTML][HTML] The infection of microvascular endothelial cells with ExoU-producing Pseudomonas aeruginosa triggers the release of von Willebrand factor and platelet …

C Freitas, MC Assis, AM Saliba, VM Morandi… - Memórias do Instituto …, 2012 - SciELO Brasil
C Freitas, MC Assis, AM Saliba, VM Morandi, CC Figueiredo, M Pereira, MC Plotkowski
Memórias do Instituto Oswaldo Cruz, 2012SciELO Brasil
An increased plasma concentration of von Willebrand factor (vWF) is detected in individuals
with many infectious diseases and is accepted as a marker of endothelium activation and
prothrombotic condition. To determine whether ExoU, a Pseudomonas aeruginosa cytotoxin
with proinflammatory activity, enhances the release of vWF, microvascular endothelial cells
were infected with the ExoU-producing PA103 P. aeruginosa strain or an exoU-deficient
mutant. Significantly increased vWF concentrations were detected in conditioned medium …
An increased plasma concentration of von Willebrand factor (vWF) is detected in individuals with many infectious diseases and is accepted as a marker of endothelium activation and prothrombotic condition. To determine whether ExoU, a Pseudomonas aeruginosa cytotoxin with proinflammatory activity, enhances the release of vWF, microvascular endothelial cells were infected with the ExoU-producing PA103 P. aeruginosa strain or an exoU-deficient mutant. Significantly increased vWF concentrations were detected in conditioned medium and subendothelial extracellular matrix from cultures infected with the wild-type bacteria, as determined by enzyme-linked immunoassays. PA103-infected cells also released higher concentrations of procoagulant microparticles containing increased amounts of membrane-associated vWF, as determined by flow cytometric analyses of cell culture supernatants. Both flow cytometry and confocal microscopy showed that increased amounts of vWF were associated with cytoplasmic membranes from cells infected with the ExoU-producing bacteria. PA103-infected cultures exposed to platelet suspensions exhibited increased percentages of cells with platelet adhesion. Because no modulation of the vWF mRNA levels was detected by reverse transcription-polymerase chain reaction assays in PA103-infected cells, ExoU is likely to have induced the release of vWF from cytoplasmic stores rather than vWF gene transcription. Such release is likely to modify the thromboresistance of microvascular endothelial cells.
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