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http://purl.uniprot.org/citations/31243731http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31243731http://www.w3.org/2000/01/rdf-schema#comment"Lower respiratory tract infection due to Pseudomonas aeruginosa has become increasingly challenging, resulting in a worse morbidity and mortality. Airway remodeling is a common phenomenon in this process, to which epithelial-mesenchymal transition (EMT) may contribute as an important promoter. Previous studies showed that epithelium-specific integrin αvβ6-mediated EMT was involved in pulmonary fibrosis via transforming growth factor-β1 (TGF-β1) signaling, but whether integrin αvβ6 plays a role in the P. aeruginosa-associated airway remodeling remains unknown. BEAS-2B cells were incubated with lipopolysaccharide (LPS) from P. aeruginosa in the presence or the absence of integrin αvβ6-blocking antibodies. Morphologic changes were observed by an inverted microscopy. The EMT markers were detected using Western blotting and immunofluorescence. The activation of TGF-β1-Smad2/3 signaling pathway was assessed. Furthermore, matrix metalloproteinase (MMP)-2 and -9 in the medium were measured using ELISA. P. aeruginosa's LPS decreased the expression of the epithelial marker E-cadherin and promoted the mesenchymal markers, vimentin and α-smooth muscle actin in BEAS-2B cells. The expression of integrin αvβ6 was significantly increased during EMT process. Blocking integrin αvβ6 could attenuate P. aeruginosa's LPS-induced EMT markers' expression via TGF-β1-Smad2/3 signaling pathway. Furthermore, blocking integrin αvβ6 could prevent morphologic changes and oversecretion of MMP-2 and -9. Integrin αvβ6 mediates epithelial-mesenchymal transition in human bronchial epithelial cells induced by lipopolysaccharides of P. aeruginosa via TGF-β1-Smad2/3 signaling pathway and might be a promising therapeutic target for P. aeruginosa-associated airway remodeling."xsd:string
http://purl.uniprot.org/citations/31243731http://purl.org/dc/terms/identifier"doi:10.1007/s12223-019-00728-w"xsd:string
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/author"Liu W."xsd:string
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/author"Sun T."xsd:string
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/name"Folia Microbiol (Praha)"xsd:string
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/pages"329-338"xsd:string
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/title"Integrin alphavbeta6 mediates epithelial-mesenchymal transition in human bronchial epithelial cells induced by lipopolysaccharides of Pseudomonas aeruginosa via TGF-beta1-Smad2/3 signaling pathway."xsd:string
http://purl.uniprot.org/citations/31243731http://purl.uniprot.org/core/volume"65"xsd:string
http://purl.uniprot.org/citations/31243731http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31243731
http://purl.uniprot.org/citations/31243731http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31243731
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