Expression and function of the endothelial protein C receptor in human neutrophils

被引:167
作者
Sturn, DH
Kaneider, NC
Feistritzer, C
Djanani, A
Fukudome, K
Wiedermann, CJ
机构
[1] Univ Innsbruck, Dept Internal Med, Div Gen Internal Med, A-6020 Innsbruck, Austria
[2] Saga Med Sch, Dept Immunol, Nabeshima, Japan
关键词
D O I
10.1182/blood-2002-12-3880
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Activation of protein C by thrombin bound to thrombomodulin is enhanced by endothelial protein C receptor. This pathway may inhibit inflammation. We investigated effects of protein C and activated protein C on neutrophils as well as whether an endothelial protein C receptor is involved in mediating protein C effects. Neutrophils were from venous blood of healthy donors. Cell migration, respiratory burst, phagocytic activity, and apoptosis were studied by micropore filter assays and fluorometry. Receptor expression was investigated by reverse transcriptase-poly m erase chain reaction (PCR) for mRNA, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDSPAGE) and autoradiography of Immunoprecipitated receptor protein, and fluorescence-activated cell-sorter scanner (FACS) analysis using the anti-endothelial protein C receptor antibody RCR-252. Neither protein C nor activated protein C induced migration, yet both of them inhibited neutrophil chemotaxis triggered by interleukin-8, formyl-Met-Leu-Phe, antithrombin, or C5a. A protein C activation-blocking antibody against endothelial protein C receptor diminished inhibitory effects of protein C or activated protein C on migration. No effect of either protein C preparation was seen in neutrophil's respiratory burst, bacterial phagocytosis, or apoptosis assays. Endothelial protein C receptor immunoreactivity was confirmed on neutrophils by FACS. De novo synthesis is suggested by endothelial protein C receptor mRNA expression as demonstrated by reverse transcriptase PCR and immunoprecipitation SDSPAGE analyses. Data suggest that an endothelial protein C receptor is expressed by human neutrophils whose active site ligation with either protein C or activated protein C arrests directed cell migration. Inhibitory effects of these components of the protein C pathway on neutrophil function may play a role in the protein C-based treatment of severe sepsis. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:1499 / 1505
页数:7
相关论文
共 40 条
[1]   Efficacy and safety of recombinant human activated protein C for severe sepsis. [J].
Bernard, GR ;
Vincent, JL ;
Laterre, P ;
LaRosa, SP ;
Dhainaut, JF ;
Lopez-Rodriguez, A ;
Steingrub, JS ;
Garber, GE ;
Helterbrand, JD ;
Ely, EW ;
Fisher, CJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :699-709
[2]   CLONING OF MOUSE MYELOMA CELLS AND DETECTION OF RARE VARIANTS [J].
COFFINO, P ;
BAUMAL, R ;
SCHARFF, MD ;
LASKOV, R .
JOURNAL OF CELLULAR PHYSIOLOGY, 1972, 79 (03) :429-&
[3]  
CONWAY EM, 1992, BLOOD, V80, P1254
[4]   Sol Sherry Lecture in Thrombosis - How thrombin 'talks' to cells - Molecular mechanisms and roles in vivo [J].
Coughlin, SR .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (04) :514-518
[5]  
Coughlin SR, 2001, THROMB HAEMOSTASIS, V86, P298
[6]   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
[7]   TREATMENT OF HOMOZYGOUS PROTEIN-C DEFICIENCY AND NEONATAL PURPURA FULMINANS WITH A PURIFIED PROTEIN-C CONCENTRATE [J].
DREYFUS, M ;
MAGNY, JF ;
BRIDEY, F ;
SCHWARZ, HP ;
PLANCHE, C ;
DEHAN, M ;
TCHERNIA, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (22) :1565-1568
[8]   Cell-surface heparan sulfate proteoglycan-mediated regulation of human neutrophil migration by the serpin antithrombin III [J].
Dunzendorfer, S ;
Kaneider, N ;
Rabensteiner, A ;
Meierhofer, C ;
Reinisch, C ;
Römisch, J ;
Wiedermann, CJ .
BLOOD, 2001, 97 (04) :1079-1085
[9]   The anticoagulant and anti-inflammatory roles of the protein C anticoagulant pathway [J].
Esmon, CT .
JOURNAL OF AUTOIMMUNITY, 2000, 15 (02) :113-116
[10]   THE REGULATION OF NATURAL ANTICOAGULANT PATHWAYS [J].
ESMON, CT .
SCIENCE, 1987, 235 (4794) :1348-1352