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dc.creatorPeppa, V. I.en
dc.creatorArsenopoulou, Z. V.en
dc.creatorZarogiannis, S. G.en
dc.creatorDeligiorgi, T.en
dc.creatorJagirdar, R.en
dc.creatorMakantasis, I.en
dc.creatorStefanidis, I.en
dc.creatorLiakopoulos, V.en
dc.creatorMolyvdas, P. A.en
dc.creatorGourgoulianis, K. I.en
dc.creatorHatzoglou, C.en
dc.date.accessioned2015-11-23T10:45:20Z
dc.date.available2015-11-23T10:45:20Z
dc.date.issued2014
dc.identifier10.1016/j.cyto.2014.06.014
dc.identifier.issn1043-4666
dc.identifier.urihttp://hdl.handle.net/11615/32146
dc.description.abstractVascular endothelial growth factor (VEGF), a cytokine that increases vascular permeability to water and proteins and induces angiogenesis, has been implicated in the development of pleural effusions. Inflammatory and malignant pleural effusions are rich in VEGF content while mesothelial cells produce and excrete VEGF. In this report we aimed at investigating by means of electrophysiology the direct effects of VEGF on the parietal and visceral sheep pleura as well as the type of receptors that mediate this effect. Our findings show that VEGF has a direct effect on the pleural mesothelium rendering it more permeable and this effect is mediated through the stimulation of VEGF receptor 2. Our findings shed more light to the role of VEGF in the pathogenesis of pleural effusions and provide functional evidence for a role of VEGFR2 on the pleural mesothelium that has never been studied before. (C) 2014 Elsevier Ltd. All rights reserved.en
dc.sourceCytokineen
dc.source.uri<Go to ISI>://WOS:000341478100017
dc.subjectMesotheliumen
dc.subjectPermeabilityen
dc.subjectPleuraen
dc.subjectVEGFen
dc.subjectVEGF receptorsen
dc.subjectENDOTHELIAL GROWTH-FACTORen
dc.subjectDIAPHRAGMATIC PARIETAL PLEURAen
dc.subjectCHAMBERen
dc.subjectEXPERIMENTSen
dc.subjectEFFUSIONSen
dc.subjectPLEURODESISen
dc.subjectPERITONEUMen
dc.subjectRESISTANCEen
dc.subjectCELLSen
dc.subjectLUNGen
dc.subjectBiochemistry & Molecular Biologyen
dc.subjectCell Biologyen
dc.subjectImmunologyen
dc.titleVEGF increases the permeability of sheep pleura ex vivo through VEGFR2 stimulationen
dc.typejournalArticleen


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