von Willebrand factor release and P-selectin expression is stimulated by thrombin and trypsin but not IL-1 in cultured human endothelial cells

• Published in: Thrombosis and haemostasis Vol. 70; no. 2; p. 346
• Main Authors: Collins, P W, Macey, M G, Cahill, M R, Newland, A C
• Format: Journal Article
• Language: English
• Published: Germany 02-08-1993
• Subjects: Cells, Cultured; Endothelium, Vascular - cytology; Endothelium, Vascular - drug effects; Endothelium, Vascular - secretion; Flow Cytometry; Fluorescent Antibody Technique; Gene Expression Regulation - drug effects; Humans; Infant, Newborn; Interleukin-1 - pharmacology; P-Selectin; Platelet Membrane Glycoproteins - biosynthesis; Stimulation, Chemical; Thrombin - pharmacology; Trypsin - pharmacology; Umbilical Veins; von Willebrand Factor - secretion
• ISSN: 0340-6245
• DOI: 10.1055/s-0038-1649578

The stimulated release of von Willebrand factor (vWF) from endothelial cells by secretagogues such as thrombin is associated with the translocation of Weibel-Palade bodies to the cell membrane and the surface expression of P-selectin (also known as GMP 140, PADGEM and CD 62). P-selectin, which is stored in Weibel-Palade bodies, is a neutrophil and monocyte adhesion molecule important in the initiation of inflammation. We have developed a simple assay for the detection of P-selectin on endothelial cells using indirect immunofluorescence and flow cytometry and have confirmed that this is temporally related to vWF release. The assay has been used to demonstrate that IL-1 does not cause Weibel-Palade body degranulation but that trypsin does. This has implications for the use of passaged endothelial cells in the study of vWF release and the assay has numerous possible applications in study of mechanisms of stimulated vWF release.