1995
Hydrogen peroxide-induced endothelial retraction is accompanied by a loss of the normal spatial organization of endothelial cell adhesion molecules.
Bradley JR, Thiru S, Pober JS. Hydrogen peroxide-induced endothelial retraction is accompanied by a loss of the normal spatial organization of endothelial cell adhesion molecules. American Journal Of Pathology 1995, 147: 627-41. PMID: 7677177, PMCID: PMC1870992.Peer-Reviewed Original ResearchConceptsMembrane protein distributionFocal adhesion plaquesAdjacent cellsNormal spatial organizationNew protein synthesisEndothelial cellsSurface protein expressionBeta 3 integrinActin organizationDendrite-like processesCell peripheryEndothelial retractionCell adhesion moleculeHuman umbilical vein endothelial cellsAdhesion plaquesUmbilical vein endothelial cellsCellular metabolismActin filamentsProtein distributionProtein synthesisVein endothelial cellsNormal endothelial cell functionEndothelial cell functionApical capCell retraction
1986
Recombinant tumor necrosis factor and immune interferon act singly and in combination to reorganize human vascular endothelial cell monolayers.
Stolpen AH, Guinan EC, Fiers W, Pober JS. Recombinant tumor necrosis factor and immune interferon act singly and in combination to reorganize human vascular endothelial cell monolayers. American Journal Of Pathology 1986, 123: 16-24. PMID: 2421578, PMCID: PMC1888144.Peer-Reviewed Original ResearchConceptsRecombinant tumor necrosis factorHuman endothelial cellsTumor necrosis factorNecrosis factorMorphologic changesRecombinant immune interferonSimilar morphologic changesUnique morphologic changesVascular endothelial cell monolayersVascular responsesEndothelial cell monolayersPrimary human endothelial cellsEndothelial cell morphologyVascular liningConfluent primary culturesEpithelioid organizationImmune interferonEndothelial cellsSpinelike processesPrimary cultures
1981
Purification of HLA-A2 antigen, fluorescent labeling of its intracellular region, and demonstration of an interaction between fluorescently labeled HLA-A2 antigen and lymphoblastoid cell cytoskeleton proteins in vitro.
Pober J, Guild B, Strominger J, Veatch W. Purification of HLA-A2 antigen, fluorescent labeling of its intracellular region, and demonstration of an interaction between fluorescently labeled HLA-A2 antigen and lymphoblastoid cell cytoskeleton proteins in vitro. Biochemistry 1981, 20: 5625-33. PMID: 6975122, DOI: 10.1021/bi00522a042.Peer-Reviewed Original Research