Plasmin-platelet interaction involves cleavage of functional thrombin receptor

被引:29
作者
Kimura, M
Andersen, TT
Fenton, JW
Bahou, WF
Aviv, A
机构
[1] ALBANY MED COLL UNION UNIV, ALBANY MED COLL, DEPT BIOCHEM & MOLEC BIOL, ALBANY, NY 12208 USA
[2] NEW YORK STATE DEPT HLTH, WADSWORTH CTR LABS & RES, ALBANY, NY 12201 USA
[3] SUNY STONY BROOK, DEPT MED, STONY BROOK, NY 11794 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1996年 / 271卷 / 01期
关键词
serine protease; cytosolic calcium; tethered peptide;
D O I
10.1152/ajpcell.1996.271.1.C54
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We tested the hypothesis that the inhibition of thrombin-induced platelet activation by plasmin is mediated via the enzymatic action of plasmin on the functional thrombin receptor. We monitored the binding of the anti-thrombin receptor antibody [anti-TR-(34-46)] to platelets; this binding is sensitive to the cleavage of the thrombin receptor at amino acid residues Arg-41 to Ser-42. Plasmin inhibited anti-TR-(34-46) binding in dose- and time-dependent manners. The inactive synthetic peptide with the amino acid sequence 40-55 of the thrombin receptor (D-FPRSFLLRNPNDKYEPF) was similarly cleaved by thrombin and plasmin to an active peptide (SFLLRNPNDKYEPF) that produced robust cytosolic Ca2+ responses. At high concentrations, plasmin itself can activate platelets. We explored this effect with the use of anti-TR-(1-160). This antibody abolished the cytosolic Ca2+ responses to thrombin and to the thrombin receptor-activating peptide SFLLRN but did not attenuate the plasmin-induced cytosolic Ca2+ response. Thus plasmin inhibits thrombin-evoked platelet activation by cleaving the thrombin receptor, but the plasmin-induced cytosolic Ca2+ response is not due to the generation of the tethered peptide of the thrombin receptor.
引用
收藏
页码:C54 / C60
页数:7
相关论文
共 21 条
[1]   THE THROMBIN RECEPTOR EXTRACELLULAR DOMAIN CONTAINS SITES CRUCIAL FOR PEPTIDE LIGAND INDUCED ACTIVATION [J].
BAHOU, WF ;
COLLER, BS ;
POTTER, CL ;
NORTON, KJ ;
KUTOK, JL ;
GOLIGORSKY, MS .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) :1405-1413
[2]   RAPID ANALYSIS OF AMINO-ACIDS USING PRE-COLUMN DERIVATIZATION [J].
BIDLINGMEYER, BA ;
COHEN, SA ;
TARVIN, TL .
JOURNAL OF CHROMATOGRAPHY, 1984, 336 (01) :93-104
[3]  
BRASS LF, 1994, J BIOL CHEM, V269, P2943
[4]   CHARACTERIZATION OF A FUNCTIONAL THROMBIN RECEPTOR - ISSUES AND OPPORTUNITIES [J].
COUGHLIN, SR ;
VU, TKH ;
HUNG, DT ;
WHEATON, VI .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (02) :351-355
[5]  
CRAMER EM, 1991, BLOOD, V77, P694
[6]  
ISHII K, 1993, J BIOL CHEM, V268, P9780
[7]  
KIMURA M, 1994, AM J PHYSIOL-CELL PH, V267, pC1543, DOI 10.1152/ajpcell.1994.267.6.C1543
[8]   SOLID PHASE PEPTIDE SYNTHESIS .1. SYNTHESIS OF A TETRAPEPTIDE [J].
MERRIFIELD, RB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (14) :2149-&
[9]   The proteinase activated receptor-2 (PAR-2) mediates mitogenic responses in human vascular endothelial cells - Molecular characterization and evidence for functional coupling to the thrombin receptor [J].
Mirza, H ;
Yatsula, V ;
Bahou, WF .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (07) :1705-1714
[10]   DUALITY OF PLASMIN EFFECT ON CYTOSOLIC-FREE CALCIUM IN HUMAN PLATELETS [J].
NAKAMURA, K ;
KIMURA, M ;
FENTON, JW ;
ANDERSEN, TT ;
AVIV, A .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 268 (04) :C958-C967