Endothelial protein C receptor-dependent inhibition of migration of human lymphocytes by protein C involves epidermal growth factor receptor

被引:41
作者
Feistritzer, C
Mosheimer, BA
Sturn, DH
Riewald, M
Patsch, JR
Wiedermann, CJ
机构
[1] Med Univ Innsbruck, Dept Internal Med, Div Gen Internal Med, A-6020 Innsbruck, Austria
[2] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
D O I
10.4049/jimmunol.176.2.1019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The protein C pathway is an important regulator of the blood coagulation system. Protein C may also play a role in inflammatory and immunomodulatory processes. Whether protein C or activated protein C affects lymphocyte migration and possible mechanisms involved was tested. Lymphocyte migration was studied by micropore filter assays. Lymphocytes that were pretreated with protein C (Ceprotin) or activated protein C (Xigris) significantly reduced their migration toward IL-8, RANTES, MCP-1, and substance P, but not toward spbingosine-1-phosphate. The inhibitory effects of protein C or activated protein C were reversed by Abs against endothelial protein C receptor and epidermal growth factor receptor. Evidence for the synthesis of endothelial protein C receptor by lymphocytes is shown by demonstration of receptor mRNA expression and detection of endothelial protein C receptor immuno reactivity on the cells' surface. Data suggest that an endothelial protein C receptor is expressed by lymphocytes whose activation with protein C or activated protein C arrests directed migration. Exposure of lymphocytes to protein C or activated protein C stimulates phosphorylation of Tyr(845) of epidermal growth factor receptor, which may be relevant for cytoprotective effects of the protein C pathway.
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收藏
页码:1019 / 1025
页数:7
相关论文
共 43 条
[1]   Signalling pathways induced by protease-activated receptors and integrins in T cells [J].
Bar-Shavit, R ;
Maoz, M ;
Yin, YJ ;
Groysman, M ;
Dekel, I ;
Katzav, S .
IMMUNOLOGY, 2002, 105 (01) :35-46
[2]   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
[3]   Activated protein C blocks p53-mediated apoptosis in ischemic human brain endothelium and is neuroprotective [J].
Cheng, T ;
Liu, D ;
Griffin, JH ;
Fernández, JA ;
Castellino, F ;
Rosen, ED ;
Fukudome, K ;
Zlokovic, BV .
NATURE MEDICINE, 2003, 9 (03) :338-342
[4]   THE WHEN AND HOW OF SRC REGULATION [J].
COOPER, JA ;
HOWELL, B .
CELL, 1993, 73 (06) :1051-1054
[5]   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
[6]  
Coughlin SR, 2001, THROMB HAEMOSTASIS, V86, P298
[7]   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
[8]   Role of transactivation of the EGF receptor in signalling by G-protein-coupled receptors [J].
Daub, H ;
Weiss, FU ;
Wallasch, C ;
Ullrich, A .
NATURE, 1996, 379 (6565) :557-560
[9]   Signal characteristics of G protein-transactivated EGF receptor [J].
Daub, H ;
Wallasch, C ;
Lankenau, A ;
Herrlich, A ;
Ullrich, A .
EMBO JOURNAL, 1997, 16 (23) :7032-7044
[10]   Protein C pathway in sepsis [J].
Esmon, CT .
ANNALS OF MEDICINE, 2002, 34 (7-8) :598-605