Haemostatic factors and atherogenesis

被引:32
作者
Smith, EB
机构
[1] Department of Clinical Biochemistry, Medical School, Foresterhill
关键词
atherogenesis; fibrin; thrombin; plasminogen activators; plasminogen activator inhibitor;
D O I
10.1016/0021-9150(96)05837-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is increasingly realised that fibrin deposition and fibrin lysis are major factors in vascular pathology. In addition to thrombotic occlusion fibrin is a component of atherosclerotic lesions, but the increased interest in components of the haemostatic system was mainly triggered by clinical use of fibrinolytic agents, and the problems of re-stenosis following angioplasty. This review focuses on the main components of the fibrinolytic system - tissue plasminogen activator (tPA), urokinase (uPA) and plasminogen activator inhibitor (PAI-1) - and on thrombin. These factors are not only involved in fluid phase clotting and clot lysis; they react specifically with cells and matrix components. During the last 5 years, the main period under review, there have been numerous studies on their interactions with endothelial and smooth muscle cells in culture, in whole tissues and in vivo, and with arterial extracellular matrix of which a major component is fibrin. Plasminogen activators bind to cell surface receptors, influence cell migration and release active thrombin from fibrin. Thrombin emerges as a pluripotent factor which modulates many aspects of endothelial and smooth muscle cell behaviour, including release and synthesis of fibrinolytic components, and stimulation of cell proliferation.
引用
收藏
页码:137 / 143
页数:7
相关论文
共 80 条
[11]  
CARMELIET P, 1995, ATHEROSCLEROSIS, V10, P45
[12]   ENHANCEMENT OF INCISIONAL WOUND-HEALING AND NEOVASCULARIZATION IN NORMAL RATS BY THROMBIN AND SYNTHETIC THROMBIN RECEPTOR-ACTIVATING PEPTIDES [J].
CARNEY, DH ;
MANN, R ;
REDIN, WR ;
PERNIA, SD ;
BERRY, D ;
HEGGERS, JP ;
HAYWARD, PG ;
ROBSON, MC ;
CHRISTIE, J ;
ANNABLE, C ;
FENTON, JW ;
GLENN, KC .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (05) :1469-1477
[13]   EFFECT OF FIBRIN STRUCTURE ON PLASMIN-MEDIATED DISSOLUTION OF PLASMA CLOTS [J].
CARR, ME ;
ALVING, BM .
BLOOD COAGULATION & FIBRINOLYSIS, 1995, 6 (06) :567-573
[14]   GROWTH-RELATED RESPONSES IN ARTERIAL SMOOTH-MUSCLE CELLS ARE ARRESTED BY THROMBIN RECEPTOR ANTISENSE SEQUENCES [J].
CHAIKOF, EL ;
CABAN, R ;
YAN, CN ;
RAO, GN ;
RUNGE, MS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) :7431-7436
[15]   SMOOTH-MUSCLE CELLS EXPRESS UROKINASE DURING MITOGENESIS AND TISSUE-TYPE PLASMINOGEN-ACTIVATOR DURING MIGRATION IN INJURED RAT CAROTID-ARTERY [J].
CLOWES, AW ;
CLOWES, MM ;
AU, YPT ;
REIDY, MA ;
BELIN, D .
CIRCULATION RESEARCH, 1990, 67 (01) :61-67
[16]   PHARMACOLOGICAL APPROACHES OF FIBRIN GEL ARCHITECTURE MODULATION AND THROMBUS DEGRADATION - ITS IMPLICATION IN ATHEROGENESIS AND THROMBOEMBOLISM DISEASE [J].
COLLET, JP ;
MISHAL, Z ;
VASSE, M ;
MIRSHAHI, M ;
CAEN, JP ;
SORIA, C ;
SORIA, J .
THROMBOSIS RESEARCH, 1994, 75 (03) :353-359
[17]   ACCESSIBILITY OF RECEPTOR-BOUND UROKINASE TO TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR [J].
CUBELLIS, MV ;
ANDREASEN, P ;
RAGNO, P ;
MAYER, M ;
DANO, K ;
BLASI, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) :4828-4832
[18]  
DAWES KE, 1993, EUR J CELL BIOL, V61, P126
[19]   MODULATION OF VASCULAR ENDOTHELIAL PERMEABILITY BY THROMBIN [J].
DEMICHELE, MAA ;
MINNEAR, FL .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1992, 18 (03) :287-295
[20]   ACCELERATION OF THE THROMBIN INACTIVATION OF SINGLE CHAIN UROKINASE-TYPE PLASMINOGEN-ACTIVATOR (PROUROKINASE) BY THROMBOMODULIN [J].
DEMUNK, GAW ;
GROENEVELD, E ;
RIJKEN, DC .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (05) :1680-1684