Proteolytically activated receptor-3 - A member of an emerging gene family of protease receptors expressed on vascular endothelial cells and platelets

被引:31
作者
Cupit, LD
Schmidt, VA
Bahou, WF
机构
[1] SUNY Stony Brook, Dept Med, Stony Brook, NY 11794 USA
[2] Amer Heart Assoc, Dallas, TX 75231 USA
[3] SUNY Stony Brook, Genet Program, Stony Brook, NY 11794 USA
关键词
D O I
10.1016/S1050-1738(99)00005-5
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Macromolecular assembly and generation of serine proteases on cellular surfaces is critically involved in regulation of hemostatic, inflammatory, or fibrinolytic pathways. The concept that a number of these serine proteases may effect cellular activation and proliferative responses has engendered an emerging paradigm focusing on the molecular mechanisms regulating cellular/protease interactions. Previous data suggest that some of these cellular responses are mediated by a novel class of G protein-coupled proteolytically activated receptors. Proteolytically activated receptor-3 (PAR-3) is the third member of this vapidly emerging gene family, all three of which (PAR-I, PAR-2, PAR-3) are known to co-cluster in the human genome, an are expressed on vascular endothelial cells, cells which critically regulate the hemostatic repertoire. This review will focus on the genetics of these receptors (emphasizing recent advances in the identification and characterization of PAR-3), review known structure/function similarities, and outline potential links in regulation of the hemostatic response by protease generation on the endothelial cell surface. (C) 1999, Elsevier Science Inc.
引用
收藏
页码:42 / 48
页数:7
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