Failure of heparin to inhibit the expression of the thrombin receptor following endothelial injury of the rabbit carotid artery

被引:7
作者
Guitteny, AF [1 ]
Herbert, JM [1 ]
机构
[1] SANOFI RECH,HAEMOBIOL RES DEPT,F-31036 TOULOUSE,FRANCE
关键词
thrombin receptor; in situ hybridization; heparin; arterial injury;
D O I
10.1016/S0014-2999(97)89655-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of heparin on thrombin receptor expression was evaluated in an experimental model of myointimal smooth muscle cell proliferation in rabbits. Myointimal hyperplasia was induced by an air-drying injury of the carotid artery and thrombin receptor expression following endothelial injury was measured by in situ hybridisation and immunohistochemistry. In healthy arteries, thrombin receptor mRNA and protein were detected in the endothelial cells only. In contrast, 14 days after endothelial injury, thrombin receptor mRNA expression increased in the smooth muscle cells present in the neointima, predominantly in areas of active cell proliferation. A 2-week subcutaneous treatment with heparin (10 mg/kg per day, s.c.) inhibited smooth muscle cell hyperplasia occurring in the intima following deendothelialization (80 +/- 7.8% inhibition, P < 0.001). The 14-day heparin treatment strongly reduced thrombin receptor gene and protein expression observed in the endothelial cells in healthy arteries but did not affect thrombin receptor expression which occurred in smooth muscle cells which have proliferated in the neointima as a consequence of endothelial injury. These results therefore establish that thrombin receptor expression during intimal hyperplasia is an heparin-insensitive event.
引用
收藏
页码:157 / 162
页数:6
相关论文
共 35 条
[1]  
AU YPT, 1992, J BIOL CHEM, V267, P3438
[2]   CHARACTERIZATION OF RAT AORTIC SMOOTH-MUSCLE CELLS RESISTANT TO THE ANTIPROLIFERATIVE ACTIVITY OF HEPARIN FOLLOWING LONG-TERM HEPARIN TREATMENT [J].
BARZU, T ;
HERBERT, JM ;
DESMOULIERE, A ;
CARAYON, P ;
PASCAL, M .
JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 160 (02) :239-248
[3]   INSITU HYBRIDIZATION HISTOCHEMISTRY FOR THE ANALYSIS OF GENE-EXPRESSION IN THE ENDOCRINE AND CENTRAL-NERVOUS-SYSTEM TISSUES - A 3-YEAR EXPERIENCE [J].
BLOCH, B ;
POPOVICI, T ;
LEGUELLEC, D ;
NORMAND, E ;
CHOUHAM, S ;
GUITTENY, AF ;
BOHLEN, P .
JOURNAL OF NEUROSCIENCE RESEARCH, 1986, 16 (01) :183-200
[4]  
BRASS LF, 1992, J BIOL CHEM, V267, P13795
[5]  
CADROY Y, 1995, THROMB HAEMOSTASIS, V75, P190
[6]   MITOGENICITY OF THROMBIN AND SURFACE ALTERATIONS ON MOUSE SPLENOCYTES [J].
CHEN, LB ;
TENG, NNH ;
BUCHANAN, JM .
EXPERIMENTAL CELL RESEARCH, 1976, 101 (01) :41-46
[7]   MITOGENIC ACTIVITY OF BLOOD COMPONENTS .1. THROMBIN AND PROTHROMBIN [J].
CHEN, LB ;
BUCHANAN, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (01) :131-135
[8]   HEPARIN INHIBITS THE EXPRESSION OF TISSUE-TYPE PLASMINOGEN-ACTIVATOR BY SMOOTH-MUSCLE CELLS IN INJURED RAT CAROTID-ARTERY [J].
CLOWES, AW ;
CLOWES, MM ;
KIRKMAN, TR ;
JACKSON, CL ;
AU, YPT ;
KENAGY, R .
CIRCULATION RESEARCH, 1992, 70 (06) :1128-1136
[9]   KINETICS OF CELLULAR PROLIFERATION AFTER ARTERIAL INJURY .4. HEPARIN INHIBITS RAT SMOOTH-MUSCLE MITOGENESIS AND MIGRATION [J].
CLOWES, AW ;
CLOWES, MM .
CIRCULATION RESEARCH, 1986, 58 (06) :839-845
[10]   THROMBIN IS AN IMPORTANT MEDIATOR OF PLATELET-AGGREGATION IN STENOSED CANINE CORONARY-ARTERIES WITH ENDOTHELIAL INJURY [J].
EIDT, JF ;
ALLISON, P ;
NOBLE, S ;
ASHTON, J ;
GOLINO, P ;
MCNATT, J ;
BUJA, LM ;
WILLERSON, JT .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (01) :18-27