<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>205(12)</volume><submitter>Nottebaum AF</submitter><pubmed_abstract>We have shown recently that vascular endothelial protein tyrosine phosphatase (VE-PTP), an endothelial-specific membrane protein, associates with vascular endothelial (VE)-cadherin and enhances VE-cadherin function in transfected cells (Nawroth, R., G. Poell, A. Ranft, U. Samulowitz, G. Fachinger, M. Golding, D.T. Shima, U. Deutsch, and D. Vestweber. 2002. EMBO J. 21:4885-4895). We show that VE-PTP is indeed required for endothelial cell contact integrity, because down-regulation of its expression enhanced endothelial cell permeability, augmented leukocyte transmigration, and inhibited VE-cadherin-mediated adhesion. Binding of neutrophils as well as lymphocytes to endothelial cells triggered rapid (5 min) dissociation of VE-PTP from VE-cadherin. This dissociation was only seen with tumor n</pubmed_abstract><journal>The Journal of experimental medicine</journal><pagination>2929-45</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2585844</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>VE-PTP maintains the endothelial barrier via plakoglobin and becomes dissociated from VE-cadherin by leukocytes and by VEGF.</pubmed_title><pmcid>PMC2585844</pmcid><pubmed_authors>Bixel MG</pubmed_authors><pubmed_authors>Cagna G</pubmed_authors><pubmed_authors>Filippova K</pubmed_authors><pubmed_authors>Butz S</pubmed_authors><pubmed_authors>Lyck R</pubmed_authors><pubmed_authors>Winderlich M</pubmed_authors><pubmed_authors>Vestweber D</pubmed_authors><pubmed_authors>Engelhardt B</pubmed_authors><pubmed_authors>Gamp AC</pubmed_authors><pubmed_authors>Polaschegg C</pubmed_authors><pubmed_authors>Kamenyeva O</pubmed_authors><pubmed_authors>Linnepe R</pubmed_authors><pubmed_authors>Nottebaum AF</pubmed_authors></additional><is_claimable>false</is_claimable><name>VE-PTP maintains the endothelial barrier via plakoglobin and becomes dissociated from VE-cadherin by leukocytes and by VEGF.</name><description>We have shown recently that vascular endothelial protein tyrosine phosphatase (VE-PTP), an endothelial-specific membrane protein, associates with vascular endothelial (VE)-cadherin and enhances VE-cadherin function in transfected cells (Nawroth, R., G. Poell, A. Ranft, U. Samulowitz, G. Fachinger, M. Golding, D.T. Shima, U. Deutsch, and D. Vestweber. 2002. EMBO J. 21:4885-4895). We show that VE-PTP is indeed required for endothelial cell contact integrity, because down-regulation of its expression enhanced endothelial cell permeability, augmented leukocyte transmigration, and inhibited VE-cadherin-mediated adhesion. Binding of neutrophils as well as lymphocytes to endothelial cells triggered rapid (5 min) dissociation of VE-PTP from VE-cadherin. This dissociation was only seen with tumor n</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Nov</publication><modification>2025-04-05T11:51:51.822Z</modification><creation>2019-03-27T00:19:27Z</creation></dates><accession>S-EPMC2585844</accession><cross_references><pubmed>19015309</pubmed><doi>10.1084/jem.20080406</doi></cross_references></HashMap>