Lipid body mobilization in the ExoU-induced release of inflammatory mediators by airway epithelial cells
This report addressed the question whether ExoU stimulation of airway epithelial cells may contribute to the inflammatory response detected in the course of Pseudomonas aeruginosa respiratory infections. Infection with PA103 P. aeruginosa elicited a potent release of IL-6 and IL-8, as well as of ara...
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Published in | Microbial pathogenesis Vol. 45; no. 1; pp. 30 - 37 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier India Pvt Ltd
01.07.2008
Elsevier |
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Abstract | This report addressed the question whether ExoU stimulation of airway epithelial cells may contribute to the inflammatory response detected in the course of
Pseudomonas aeruginosa respiratory infections. Infection with PA103
P. aeruginosa elicited a potent release of IL-6 and IL-8, as well as of arachidonic acid (AA) and PGE
2 that was reduced by the bacterial treatment with MAFP, a cPLA
2 inhibitor. Airway cells from the BEAS-2B line and in primary culture were shown to be enriched in lipid bodies (LBs), that are cytoplasmic domains implicated in AA transformation into eicosanoids. However, cells infected with PA103 and with a mutant deficient in
exoU but complemented with a functional gene exhibited reduced contents of LBs, and this reduction was inhibited by MAFP. FACS analysis showed that the decrease in the LB content correlated with the presence of intracellular PGE
2. Also, in PA103-infected cells, PGE
2 was immunolocalized in LBs, suggesting that the reduction in the cell content of the organelles was due to consumption of their glycerolipids, resulting in local synthesis of the prostanoid. In conclusion, we showed the ExoU ability to induce airway epithelial cells to overproduce PGE
2 and we speculate that LB may represent intracellular loci involved in ExoU-induced eicosanoid synthesis. |
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AbstractList | This report addressed the question whether ExoU stimulation of airway epithelial cells may contribute to the inflammatory response detected in the course of Pseudomonas aeruginosa respiratory infections. Infection with PA103 P. aeruginosa elicited a potent release of IL-6 and IL-8, as well as of arachidonic acid (AA) and PGE(2) that was reduced by the bacterial treatment with MAFP, a cPLA(2) inhibitor. Airway cells from the BEAS-2B line and in primary culture were shown to be enriched in lipid bodies (LBs), that are cytoplasmic domains implicated in AA transformation into eicosanoids. However, cells infected with PA103 and with a mutant deficient in exoU but complemented with a functional gene exhibited reduced contents of LBs, and this reduction was inhibited by MAFP. FACS analysis showed that the decrease in the LB content correlated with the presence of intracellular PGE(2). Also, in PA103-infected cells, PGE(2) was immunolocalized in LBs, suggesting that the reduction in the cell content of the organelles was due to consumption of their glycerolipids, resulting in local synthesis of the prostanoid. In conclusion, we showed the ExoU ability to induce airway epithelial cells to overproduce PGE(2) and we speculate that LB may represent intracellular loci involved in ExoU-induced eicosanoid synthesis. This report addressed the question whether ExoU stimulation of airway epithelial cells may contribute to the inflammatory response detected in the course of Pseudomonas aeruginosa respiratory infections. Infection with PA103 P. aeruginosa elicited a potent release of IL-6 and IL-8, as well as of arachidonic acid (AA) and PGE sub(2) that was reduced by the bacterial treatment with MAFP, a cPLA sub(2) inhibitor. Airway cells from the BEAS-2B line and in primary culture were shown to be enriched in lipid bodies (LBs), that are cytoplasmic domains implicated in AA transformation into eicosanoids. However, cells infected with PA103 and with a mutant deficient in exoU but complemented with a functional gene exhibited reduced contents of LBs, and this reduction was inhibited by MAFP. FACS analysis showed that the decrease in the LB content correlated with the presence of intracellular PGE sub(2). Also, in PA103-infected cells, PGE sub(2) was immunolocalized in LBs, suggesting that the reduction in the cell content of the organelles was due to consumption of their glycerolipids, resulting in local synthesis of the prostanoid. In conclusion, we showed the ExoU ability to induce airway epithelial cells to overproduce PGE sub(2) and we speculate that LB may represent intracellular loci involved in ExoU-induced eicosanoid synthesis. This report addressed the question whether ExoU stimulation of airway epithelial cells may contribute to the inflammatory response detected in the course of Pseudomonas aeruginosa respiratory infections. Infection with PA103 P. aeruginosa elicited a potent release of IL-6 and IL-8, as well as of arachidonic acid (AA) and PGE 2 that was reduced by the bacterial treatment with MAFP, a cPLA 2 inhibitor. Airway cells from the BEAS-2B line and in primary culture were shown to be enriched in lipid bodies (LBs), that are cytoplasmic domains implicated in AA transformation into eicosanoids. However, cells infected with PA103 and with a mutant deficient in exoU but complemented with a functional gene exhibited reduced contents of LBs, and this reduction was inhibited by MAFP. FACS analysis showed that the decrease in the LB content correlated with the presence of intracellular PGE 2. Also, in PA103-infected cells, PGE 2 was immunolocalized in LBs, suggesting that the reduction in the cell content of the organelles was due to consumption of their glycerolipids, resulting in local synthesis of the prostanoid. In conclusion, we showed the ExoU ability to induce airway epithelial cells to overproduce PGE 2 and we speculate that LB may represent intracellular loci involved in ExoU-induced eicosanoid synthesis. |
Author | de Assis, Maria-Cristina Raymond, Benoit Bozza, Patrícia T. Plotkowski, Maria-Cristina Freitas, Carla Touqui, Lhousseine Saliba, Alessandra M. Brandão, Bruno A. Feliciano, Luis-Filipe P. Zahm, Jean Marie |
Author_xml | – sequence: 1 givenname: Maria-Cristina surname: Plotkowski fullname: Plotkowski, Maria-Cristina email: crisplot@yahoo.com.br organization: Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Avenue 28 de Setembro, 87 Fundos, 3° andar, 20 551-030, Rio de Janeiro, Brazil – sequence: 2 givenname: Bruno A. surname: Brandão fullname: Brandão, Bruno A. organization: Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Avenue 28 de Setembro, 87 Fundos, 3° andar, 20 551-030, Rio de Janeiro, Brazil – sequence: 3 givenname: Maria-Cristina surname: de Assis fullname: de Assis, Maria-Cristina organization: Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Avenue 28 de Setembro, 87 Fundos, 3° andar, 20 551-030, Rio de Janeiro, Brazil – sequence: 4 givenname: Luis-Filipe P. surname: Feliciano fullname: Feliciano, Luis-Filipe P. organization: Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Avenue 28 de Setembro, 87 Fundos, 3° andar, 20 551-030, Rio de Janeiro, Brazil – sequence: 5 givenname: Benoit surname: Raymond fullname: Raymond, Benoit organization: Institut Pasteur, Unité de Defense Innée et Inflammation, INSERM U 874, Paris, France – sequence: 6 givenname: Carla surname: Freitas fullname: Freitas, Carla organization: Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Avenue 28 de Setembro, 87 Fundos, 3° andar, 20 551-030, Rio de Janeiro, Brazil – sequence: 7 givenname: Alessandra M. surname: Saliba fullname: Saliba, Alessandra M. organization: Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Avenue 28 de Setembro, 87 Fundos, 3° andar, 20 551-030, Rio de Janeiro, Brazil – sequence: 8 givenname: Jean Marie surname: Zahm fullname: Zahm, Jean Marie organization: INSERM U 903, Université de Reims Champagne-Ardenne, Reims, France – sequence: 9 givenname: Lhousseine surname: Touqui fullname: Touqui, Lhousseine organization: Institut Pasteur, Unité de Defense Innée et Inflammation, INSERM U 874, Paris, France – sequence: 10 givenname: Patrícia T. surname: Bozza fullname: Bozza, Patrícia T. organization: Departamento de Fisiologia e Farmacodinâmica, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro, Brazil |
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Keywords | ExoU PGE2 Pseudomonas aeruginosa Inflammatory response Lipid body Arachidonic acid Pseudomonadales Microbiology Lipids Inflammation Respiratory system Pseudomonas aeruginosa,ExoU,Lipid body,Inflammatory response,Arachidonic acid,PGE2 Respiratory tract Bacteria Pseudomonadaceae Epithelial cell Inflammatory cell Release |
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SubjectTerms | Arachidonic Acid Arachidonic Acid - metabolism Arachidonic Acids Arachidonic Acids - pharmacology Bacterial Proteins Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacteriology Biological and medical sciences Bronchi Bronchi - cytology Bronchi - drug effects Bronchi - metabolism Bronchi - microbiology Cell Line Cytokines Cytokines - metabolism Enzyme Inhibitors Enzyme Inhibitors - pharmacology Epithelial Cells Epithelial Cells - cytology Epithelial Cells - drug effects Epithelial Cells - metabolism Epithelial Cells - microbiology ExoU Fundamental and applied biological sciences. Psychology Human health and pathology Humans Inclusion Bodies Inclusion Bodies - metabolism Inflammation Mediators Inflammation Mediators - metabolism Inflammatory response Life Sciences Lipid body Lipid Metabolism Microbiology Miscellaneous Organophosphonates - pharmacology PGE2 Phosphonic Acids Prostaglandins E Prostaglandins E - metabolism Pseudomonas aeruginosa Pseudomonas aeruginosa - drug effects Pseudomonas aeruginosa - metabolism Pseudomonas Infections Pseudomonas Infections - metabolism Pulmonology and respiratory tract |
Title | Lipid body mobilization in the ExoU-induced release of inflammatory mediators by airway epithelial cells |
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