1
Medizinische Klinik III, Eberhard Karls University Tuebingen, Tuebingen, Germany
,
Björn Krämer
1
Medizinische Klinik III, Eberhard Karls University Tuebingen, Tuebingen, Germany
,
Boris Bigalke
1
Medizinische Klinik III, Eberhard Karls University Tuebingen, Tuebingen, Germany
,
Berthold Büchele
4
Institute of Pharmacololgy of Natural Products and Clinical Pharmacology, Ulm University, Ulm, Germany
,
Max G. Bachem
5
Department of Clinical Chemistry and Pathobiochemistry, University of Ulm, Ulm, Germany
,
Dietmar Vestweber
6
Department of Vascular Cell Biology, Max-Planck Institute for Molecular Biomedicine, Münster, Germany
,
Thomas Simmet
4
Institute of Pharmacololgy of Natural Products and Clinical Pharmacology, Ulm University, Ulm, Germany
,
Meinrad Gawaz
1
Medizinische Klinik III, Eberhard Karls University Tuebingen, Tuebingen, Germany
,
Andreas E. May
1
Medizinische Klinik III, Eberhard Karls University Tuebingen, Tuebingen, Germany
› Author AffiliationsFinancial support: Financial support: This study was supported by the Wilhelm-Sander-Stiftung Nr. 2006.059.1 (to PS, AEM), the Novartis-Stiftung (to HL, AEM and MG), the Deutsche Forschungsgemeinschaft SFB-TR19 (to AEM and MG) and by a research grant from the German Cardiac Society (Pfizer Stipendium) to HL.
The Extracellular Matrix Metalloproteinase Inducer (EMMPRIN, CD147, basigin) is an immunoglobulin-like receptor expressed in various cell types. During cellular interactions homotypic EMMPRIN-EMMPRIN interactions are known to induce the synthesis of matrix metalloproteinases. Recently, we have identified EMMPRIN as a novel receptor on platelets. To our knowledge EMMPRIN has not been shown to serve as adhesion receptor, yet. Here we characterise platelet glycoprotein VI (GPVI) as a novel adhesion receptor for EMMPRIN. Human platelets were prestimulated with ADP and perfused over immobilised recombinant EMMPRIN-Fc or Fc-fragments under arterial shear conditions. ADP-stimulated platelets showed significantly enhanced rolling (but not enhanced firm adhesion) on immobilised EMMPRIN-Fc compared to Fc. Pretreatment of platelets with blocking mAbs anti-EMMPRIN or anti-GPVI leads to a significant reduction of rolling platelets on immobilised EMMPRIN-Fc, whereas pretreatment with blocking mAbs anti-p-selectin, anti-α4-integrin or anti-GPIIb/IIIa complex (20 μg/ml each) had no effect. Consistently, chinese hamster ovary (CHO) cells stably transfected with GPVI showed enhanced rolling (but not adhesion) on immobilised EMMPRIN-Fc in comparison to nontransfected CHO cells. Similarly, CHO cells stably transfected with EMMPRIN showed enhanced rolling on immobilised GPVIFc (or EMMPRIN-Fc) compared to non transfected CHO-cells. Finally, specific binding of EMMPRIN to GPVI was demonstrated by a modified ELISA and surface plasmon resonance technology with a dissociation constant of 88 nM. Platelet GPVI is a novel receptor for EMMPRIN and can mediate platelet rolling via GPVIEMMPRIN interaction.
Keywords
EMMPRIN, GPVI, platelets, atherosclerosis
References
1
Toole BP.
Emmprin (CD147), a cell surface regulator of matrix metalloproteinase production and function. Curr Top Dev Biol 2003; 54: 371-389.
2
Schmidt R,
Bultmann A,
Fischel S.
et al.
Extracellular matrix metalloproteinase inducer (CD147) is a novel receptor on platelets, activates platelets, and augments nuclear factor kappaB-dependent inflammation in monocytes. Circ Res 2008; 102: 302-309.
3
Massberg S,
Konrad I,
Bultmann A.
et al.
Soluble glycoprotein VI dimer inhibits platelet adhesion and aggregation to the injured vessel wall in vivo. FASEB J 2004; 18: 397-399.
4
Guo H,
Zucker S,
Gordon MK.
et al.
Stimulation of matrix metalloproteinase production by recombinant extracellular matrix metalloproteinase inducer from transfected Chinese hamster ovary cells. J Biol Chem 1997; 272: 24-27.
6
Hahne M,
Jager U,
Isenmann S.
et al.
Five tumor necrosis factor-inducible cell adhesion mechanisms on the surface of mouse endothelioma cells mediate the binding of leukocytes. J Cell Biol 1993; 121: 655-664.
7
Schneiderhan W,
Diaz F,
Fundel M.
et al.
Pancreatic stellate cells are an important source of MMP-2 in human pancreatic cancer and accelerate tumor progression in a murine xenograft model and CAM assay. J Cell Sci 2007; 120: 512-519.
9
Bigalke B,
Lindemann S,
Ehlers R.
et al.
Expression of platelet collagen receptor glycoprotein VI is associated with acute coronary syndrome. Eur Heart J 2006; 27: 2165-2169.