Regulation of coagulation by protein S

被引:108
作者
Castoldi, Elisabetta [1 ]
Hackeng, Tilman M. [1 ]
机构
[1] Maastricht Univ, Dept Biochem, Cardiovasc Res Inst Maastricht CARIM, NL-6200 MD Maastricht, Netherlands
关键词
activated protein C; protein S deficiency; protein S-C4b-binding protein; thrombosis; tissue factor pathway inhibitor;
D O I
10.1097/MOH.0b013e328309ec97
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Protein S has been one of the least mechanistically understood amongst the vitamin K-dependent coagulation proteins, and diagnosis of protein S deficiency and quantification of the associated thrombotic risk are not straightforward. In this review, the regulation of thrombin generation by protein S and the pathophysiological implications of protein S deficiency are discussed in the light of recent findings on the anticoagulant function(s) of protein S. Recent findings Protein S expresses both activated protein C-dependent and activated protein C-independent anticoagulant activities, but the former is generally believed to be lost upon binding of protein S to C4b-binding protein. Recently it has been shown that protein S acts as a cofactor of tissue factor pathway inhibitor in the down regulation of factor X-activation, which provides a mechanistic basis for the activated protein C-independent anticoagulant activity of protein S in plasma. In addition, reevaluation of the role of the protein S/C4b-binding protein complex has demonstrated that C4b-binding protein-bound protein S does express activated protein C-cofactor activity, especially during the inactivation of factor Va Leiden. Summary These findings underscore the central role of protein S in the regulation of coagulation and may have important implications for the evaluation of the thrombotic risk associated with protein S deficiency.
引用
收藏
页码:529 / 536
页数:8
相关论文
共 96 条
[1]   A quantitative trait locus influencing free plasma protein S levels on human chromosome 1q -: Results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) project [J].
Almasy, L ;
Soria, JM ;
Souto, JC ;
Bacq, ICD ;
Faure, A ;
Mateo, J ;
Borrell, M ;
Muñoz, X ;
Sala, N ;
Stone, WH ;
Lathrop, M ;
Fontcuberta, J ;
Blangero, J .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (03) :508-511
[2]   Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function [J].
Baroni, M ;
Mazzola, G ;
Kaabache, T ;
Borgel, D ;
Gandrille, S ;
D'Angelo, SV ;
Marchetti, G ;
di Iasio, MG ;
Pinotti, M ;
D'Angelo, A ;
Bernardi, F .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (01) :186-191
[3]  
Beauchamp NJ, 1996, BLOOD, V88, P1700
[4]   The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population [J].
Beauchamp, NJ ;
Dykes, AC ;
Parikh, N ;
Tait, RC ;
Daly, ME .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 125 (05) :647-654
[5]  
BERTINA RM, 1990, BLOOD, V76, P538
[6]   Molecular diversity and thrombotic risk in Protein S deficiency: The PROSIT study [J].
Biguzzi, E ;
Razzari, C ;
Lane, DA ;
Castaman, G ;
Cappellari, A ;
Bucciarelli, P ;
Fontana, G ;
Margaglione, M ;
D'Andrea, G ;
Simmonds, RE ;
Rezende, SM ;
Preston, R ;
Prisco, D ;
Faioni, EM .
HUMAN MUTATION, 2005, 25 (03) :259-269
[7]   Cleaved protein S (PS), total PS, free PS, and activated protein C cofactor activity as risk factors for venous thromboembolism [J].
Borgel, D ;
Reny, JL ;
Fischelis, D ;
Gandrille, S ;
Emmerich, J ;
Fiessinger, JN ;
Aiach, M .
CLINICAL CHEMISTRY, 2003, 49 (04) :575-580
[8]   Difference in absolute risk of venous and arterial thrombosis between familial protein S deficiency type I and type III. Results from a family cohort study to assess the clinical impact of a laboratory test-based classification [J].
Brouwer, JLP ;
Veeger, NJGM ;
van der Schaaf, W ;
Kluin-Nelemans, HC ;
van der Meer, J .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 128 (05) :703-710
[9]  
BROZE GJ, 1988, BLOOD, V71, P335
[10]   Protein S levels modulate the activated protein C resistance phenotype induced by elevated prothrombin levels [J].
Brugge, JM ;
Tans, G ;
Rosing, J ;
Castoldi, E .
THROMBOSIS AND HAEMOSTASIS, 2006, 95 (02) :236-242