Protease-activated Receptors in Vascular Biology
- 1 January 2001
- journal article
- research article
- Published by Georg Thieme Verlag KG in Thrombosis and Haemostasis
- Vol. 86 (07) , 298-307
- https://doi.org/10.1055/s-0037-1616227
Abstract
G protein-coupled protease-activated receptors (PARs) provide one answer to the question of how coagulation factors and other proteases regulate cellular behaviors. In concert with the coagulation cascade, these receptors provide an elegant mechanism that links mechanical information in the form of tissue injury or vascular leak to cellular responses. Roles for PARs in hemostasis and thrombosis, inflammation, and perhaps even blood vessel development are beginning to emerge. Our current understanding of the role of PARs in platelet and endothelial cell activation and their potential importance in normal and disease states is discussed.Keywords
This publication has 54 references indexed in Scilit:
- Binding of Thrombin to Glycoprotein Ib Accelerates the Hydrolysis of Par-1 on Intact PlateletsPublished by Elsevier ,2001
- Direct Stimulation of the Guanine Nucleotide Exchange Activity of p115 RhoGEF by Gα 13Science, 1998
- Protease-activated receptor 3 is a second thrombin receptor in humansNature, 1997
- Coagulation Factors VII and X Induce Ca2+ Oscillations in Madin-Darby Canine Kidney Cells Only When Proteolytically ActiveJournal of Biological Chemistry, 1996
- Fatal haemorrhage and incomplete block to embryogenesis in mice lacking coagulation factor VNature, 1996
- Thrombin functions as an inflammatory mediator through activation of its receptor.The Journal of Experimental Medicine, 1996
- Thrombin Primes Responsiveness of Selective Chemoattractant Receptors at a Site Distal to G Protein ActivationJournal of Biological Chemistry, 1996
- Domains specifying thrombin–receptor interactionNature, 1991
- Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activationCell, 1991
- Variant Bernard-Soulier syndrome type bolzano. A congenital bleeding disorder due to a structural and functional abnormality of the platelet glycoprotein Ib-IX complex.Journal of Clinical Investigation, 1990