Serpins in thrombosis, hemostasis and fibrinolysis

被引:246
作者
Rau, J. C.
Beaulieu, L. M.
Huntington, J. A.
Church, F. C.
机构
[1] Univ N Carolina, Dept Pathol & Lab Med, Carolina Cardiovasc Biol Ctr, Sch Med, Chapel Hill, NC 27599 USA
[2] Univ Cambridge, Dept Haematol, Div Struct Med, Thrombosis Res Unit,Cambridge Inst Med Res,Wellco, Cambridge, England
基金
英国医学研究理事会;
关键词
alpha(1)-protease inhibitor; alpha(2)-antiplasmin; antithrombin; fibrinolysis; hemostasis; heparin; heparin cofactor II; plasminogen activator inhibitor-1; protein C inhibitor; protein Z-dependent protease inhibitor; serpins; thrombosis;
D O I
10.1111/j.1538-7836.2007.02516.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hemostasis and fibrinolysis, the biological processes that maintain proper blood flow, are the consequence of a complex series of cascading enzymatic reactions. Serine proteases involved in these processes are regulated by feedback loops, local cofactor molecules, and serine protease inhibitors (serpins). The delicate balance between proteolytic and inhibitory reactions in hemostasis and fibrinolysis, described by the coagulation, protein C and fibrinolytic pathways, can be disrupted, resulting in the pathological conditions of thrombosis or abnormal bleeding. Medicine capitalizes on the importance of serpins, using therapeutics to manipulate the serpin-protease reactions for the treatment and prevention of thrombosis and hemorrhage. Therefore, investigation of serpins, their cofactors, and their structure-function relationships is imperative for the development of state-of-the-art pharmaceuticals for the selective fine-tuning of hemostasis and fibrinolysis. This review describes key serpins important in the regulation of these pathways: antithrombin, heparin cofactor II, protein Z-dependent protease inhibitor, alpha(1)-protease inhibitor, protein C inhibitor, alpha(2)-antiplasmin and plasminogen activator inhibitor-1. We focus on the biological function, the important structural elements, their known non-hemostatic roles, the pathologies related to deficiencies or dysfunction, and the therapeutic roles of specific serpins.
引用
收藏
页码:102 / 115
页数:14
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