A SULFATED RABBIT ENDOTHELIAL-CELL GLYCOPROTEIN THAT INHIBITS FACTOR-VIIA TISSUE FACTOR IS FUNCTIONALLY AND IMMUNOLOGICALLY IDENTICAL TO RABBIT EXTRINSIC PATHWAY INHIBITOR (EPI)

被引:23
作者
WARNCRAMER, BJ [1 ]
MAKI, SL [1 ]
RAPAPORT, SI [1 ]
机构
[1] UNIV CALIF SAN DIEGO,DEPT PATHOL,LA JOLLA,CA 92093
关键词
EXTRINSIC PATHWAY INHIBITOR; FACTOR-VII; TISSUE FACTOR; FACTOR-X; ENDOTHELIAL CELLS; RABBITS;
D O I
10.1016/0049-3848(91)90159-T
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Colburn and Buonassisi (In Vitro Cell Dev. Biol. 24, 1133-1136, 1988) have isolated a single chain sulfated glycoprotein inhibitor of factor VIIa/tissue factor-catalyzed activation of factor X from conditioned media of an established rabbit endothelial cell line. We report herein that their endothelial cell-derived inhibitor and extrinsic pathway inhibitor (EPI) isolated from rabbit plasma have identical functional properties with respect to their interactions with factor Xa and with factor VIIa/tissue factor. In addition, the endothelial cell inhibitor and rabbit plasma EPI migrate with the same apparent molecular weights on non-reduced SDS-PAGE and contain similar amounts of N-linked carbohydrate. Like the endothelial cell inhibitor the EPI of rabbit plasma exists as a single chain molecule. Furthermore, the endothelial cell inhibitor is recognized and neutralized by a polyclonal antibody raised against rabbit plasma EPI. We therefore conclude that cultured rabbit endothelial cells produce an inhibitor of factor VIIa/tissue factor activity that is functionally and immunologically identical to rabbit plasma EPI.
引用
收藏
页码:515 / 527
页数:13
相关论文
共 29 条
[1]   INHIBITOR OF THE FACTOR-VIIA-TISSUE FACTOR COMPLEX IS REDUCED IN PATIENTS WITH DISSEMINATED INTRAVASCULAR COAGULATION BUT NOT IN PATIENTS WITH SEVERE HEPATOCELLULAR DISEASE [J].
BAJAJ, MS ;
RANA, SV ;
WYSOLMERSKI, RB ;
BAJAJ, SP .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (06) :1874-1878
[2]   A SIMPLIFIED PROCEDURE FOR PURIFICATION OF HUMAN-PROTHROMBIN, FACTOR-IX AND FACTOR-X [J].
BAJAJ, SP ;
RAPAPORT, SI ;
PRODANOS, C .
PREPARATIVE BIOCHEMISTRY, 1981, 11 (04) :397-412
[3]  
BROZE GJ, 1988, BLOOD, V71, P335
[4]   REGULATION OF COAGULATION BY A MULTIVALENT KUNITZ-TYPE INHIBITOR [J].
BROZE, GJ ;
GIRARD, TJ ;
NOVOTNY, WF .
BIOCHEMISTRY, 1990, 29 (33) :7539-7546
[5]  
BROZE GJ, 1987, BLOOD, V69, P150
[6]   ISOLATION OF THE TISSUE FACTOR INHIBITOR PRODUCED BY HEPG2 HEPATOMA-CELLS [J].
BROZE, GJ ;
MILETICH, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (07) :1886-1890
[7]  
COLBURN P, 1988, IN VITRO CELL DEV B, V24, P1133
[8]   FUNCTIONAL-SIGNIFICANCE OF THE KUNITZ-TYPE INHIBITORY DOMAINS OF LIPOPROTEIN-ASSOCIATED COAGULATION INHIBITOR [J].
GIRARD, TJ ;
WARREN, LA ;
NOVOTNY, WF ;
LIKERT, KM ;
BROWN, SG ;
MILETICH, JP ;
BROZE, GJ .
NATURE, 1989, 338 (6215) :518-520
[9]   INHIBITION OF THE TISSUE FACTOR-FACTOR-VII COMPLEX - INVOLVEMENT OF FACTOR XA AND LIPOPROTEINS [J].
HUBBARD, AR ;
JENNINGS, CA .
THROMBOSIS RESEARCH, 1987, 46 (04) :527-537
[10]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+