Semin Thromb Hemost 2010; 36(2): 146-156
DOI: 10.1055/s-0030-1251498
© Thieme Medical Publishers

Oxidized LDL-Activated Platelets Induce Vascular Inflammation

Karin Daub1 , Peter Seizer1 , Konstantinos Stellos1 , Björn F. Krämer1 , Boris Bigalke1 , Martin Schaller2 , Suzanne Fateh-Moghadam1 , Meinrad Gawaz1 , Stephan Lindemann1
  • 1Medizinische Klinik, Klinik für Kardiologie und Kreislauferkrankungen, Eberhard-Karls-Universität Tübingen, Germany
  • 2Hautklinik, Eberhard-Karls-Universität Tübingen, Germany
Further Information

Publication History

Publication Date:
22 April 2010 (online)

ABSTRACT

Platelets are involved in the initiation of atherosclerosis by adherence to inflamed endothelium. Monocytes bind to these platelets and transmigrate into the vessel wall, transforming into macrophages and foam cells. We have previously shown that lipid-laden platelets are phagocytosed by macrophages. In this study we investigated the functional consequences of oxidized low-density lipoprotein (oxLDL) uptake on platelet function and interaction with the endothelium. Human platelets were isolated from healthy donors and activated by adenosine diphosphate. Immunofluorescence microscopy and flow cytometry revealed that oxLDL is located intracellularly in vesicles. With mepacrine costaining and confocal microtomography, we were able to identify dense granules as the vesicles that contain oxLDL. OxLDL-laden platelets induced intercellular adhesion molecule 1 expression in endothelial cells more than exogenous native LDL, oxLDL, and oxLDL-negative platelets. Furthermore, oxLDL-laden platelets induced foam cell development from CD34+ progenitor cells. On endothelial regeneration, oxLDL-laden platelets had the opposite effect: The number of CD34+ progenitor cells (colony-forming units) able to transform into endothelial cells was significantly reduced in the presence of oxLDL-platelets, whereas native LDL had no effect. Our results demonstrate that activated platelets internalize oxLDL and that oxLDL-laden platelets activate endothelium, inhibit endothelial regeneration, and promote foam cell development. Platelet oxLDL contributes significantly to vascular inflammation and is able to promote atherosclerosis.

REFERENCES

  • 1 Massberg S, Brand K, Grüner S et al.. A critical role of platelet adhesion in the initiation of atherosclerotic lesion formation.  J Exp Med. 2002;  196(7) 887-896
  • 2 Ruggeri Z M. Platelets in atherothrombosis.  Nat Med. 2002;  8 1227-1234
  • 3 Gawaz M, Langer H, May A E. Platelets in inflammation and atherogenesis.  J Clin Invest. 2005;  115(12) 3378-3384
  • 4 Gawaz M. Role of platelets in coronary thrombosis and reperfusion of ischemic myocardium.  Cardiovasc Res. 2004;  61(3) 498-511
  • 5 Massberg S, Enders G, Leiderer R et al.. Platelet-endothelial cell interactions during ischemia/reperfusion: the role of P-selectin.  Blood. 1998;  92(2) 507-515
  • 6 Burger P C, Wagner D D. Platelet P-selectin facilitates atherosclerotic lesion development.  Blood. 2003;  101(7) 2661-2666
  • 7 Siegel-Axel D, Langer H, Lindemann S, Gawaz M. Role of platelets in atherosclerosis and inflammation [in German].  Med Klin (Munich). 2006;  101(6) 467-475
  • 8 Lusis A J. Atherosclerosis.  Nature. 2000;  407(6801) 233-241
  • 9 Daub K, Langer H, Seizer P et al.. Platelets induce differentiation of human CD34+ progenitor cells into foam cells and endothelial cells.  FASEB J. 2006;  20 2559-2561
  • 10 Engelmann B, Kögl C, Kulschar R, Schaipp B. Transfer of phosphatidylcholine, phosphatidylethanolamine and sphingomyelin from low- and high-density lipoprotein to human platelets.  Biochem J. 1996;  315(Pt 3) 781-789
  • 11 Asch A S, Silbiger S, Heimer E, Nachman R L. Thrombospondin sequence motif (CSVTCG) is responsible for CD36 binding.  Biochem Biophys Res Commun. 1992;  182(3) 1208-1217
  • 12 Tandon N N, Kralisz U, Jamieson G A. Identification of glycoprotein IV (CD36) as a primary receptor for platelet-collagen adhesion.  J Biol Chem. 1989;  264(13) 7576-7583
  • 13 Aiken M L, Ginsberg M H, Byers-Ward V, Plow E F. Effects of OKM5, a monoclonal antibody to glycoprotein IV, on platelet aggregation and thrombospondin surface expression.  Blood. 1990;  76(12) 2501-2509
  • 14 Marcus A J, Silk S T, Safier L B, Ullman H L. Superoxide production and reducing activity in human platelets.  J Clin Invest. 1977;  59(1) 149-158
  • 15 Gawaz M, Neumann F J, Schomig A. Evaluation of platelet membrane glycoproteins in coronary artery disease: consequences for diagnosis and therapy.  Circulation. 1999;  99(1) E1-E11
  • 16 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(18) 2165-2169
  • 17 Roth D R, Axel D I, Betz E L. In vitro model of the inner parts of a vessel wall with cultured human vascular cells.  Coron Artery Dis. 1993;  4 283-291
  • 18 Axel D I, Brehm B R, Wolburg-Buchholz K, Betz E L, Köveker G, Karsch K R. Induction of cell-rich and lipid-rich plaques in a transfilter coculture system with human vascular cells.  J Vasc Res. 1996;  33(4) 327-339
  • 19 Langer H, May A E, Daub K et al.. Adherent platelets recruit and induce differentiation of murine embryonic endothelial progenitor cells to mature endothelial cells in vitro.  Circ Res. 2006;  98(2) e2-e10
  • 20 Gawaz M, Brand K, Dickfeld T et al.. Platelets induce alterations of chemotactic and adhesive properties of endothelial cells mediated through an interleukin-1-dependent mechanism. Implications for atherogenesis.  Atherosclerosis . 2000;  148 75-85
  • 21 Weyrich A, Cipollone F, Mezzetti A et al.. Platelets in atherothrombosis: new and evolving roles.  Curr Pharm Des. 2007;  13 1685-1691
  • 22 Massberg S, Brand K, Grüner S et al.. A critical role of platelet adhesion in the initiation of atherosclerotic lesion formation.  J Exp Med. 2002;  196(7) 887-896
  • 23 Steinberg D. Low density lipoprotein oxidation and its pathobiological significance.  J Biol Chem. 1997;  272(34) 20963-20966
  • 24 Ammon C, Kreutz M, Rehli M, Krause S W, Andreesen R. Platelets induce monocyte differentiation in serum-free coculture.  J Leukoc Biol. 1998;  63(4) 469-476
  • 25 Relou I A, Hackeng C M, Akkerman J W, Malle E. Low-density lipoprotein and its effect on human blood platelets.  Cell Mol Life Sci. 2003;  60(5) 961-971
  • 26 Pedreño J, Hurt-Camejo E, Wiklund O, Badimón L, Masana L. Low-density lipoprotein (LDL) binds to a G-protein coupled receptor in human platelets. Evidence that the proaggregatory effect induced by LDL is modulated by down-regulation of binding sites and desensitization of its mediated signaling.  Atherosclerosis. 2001;  155(1) 99-112
  • 27 Hartwich J, Dembinska-Kieć A, Gruca A et al.. Regulation of platelet adhesion by oxidized lipoproteins and oxidized phospholipids.  Platelets. 2002;  13(3) 141-151
  • 28 Dardik R, Varon D, Tamarin I et al.. Homocysteine and oxidized low density lipoprotein enhanced platelet adhesion to endothelial cells under flow conditions: distinct mechanisms of thrombogenic modulation.  Thromb Haemost. 2000;  83(2) 338-344
  • 29 Carnevale R, Pignatelli P, Lenti L et al.. LDL are oxidatively modified by platelets via GP91(phox) and accumulate in human monocytes.  FASEB J. 2007;  21(3) 927-934
  • 30 Korporaal S J, Gorter G, van Rijn H J, Akkerman J W. Effect of oxidation on the platelet-activating properties of low-density lipoprotein.  Arterioscler Thromb Vasc Biol. 2005;  25(4) 867-872
  • 31 Krötz F, Sohn H Y, Gloe T et al.. NAD(P)H oxidase-dependent platelet superoxide anion release increases platelet recruitment.  Blood. 2002;  100(3) 917-924
  • 32 Pignatelli P, Sanguigni V, Lenti L et al.. Oxidative stress-mediated platelet CD40 ligand upregulation in patients with hypercholesterolemia: effect of atorvastatin.  J Thromb Haemost. 2007;  5 1170-1178
  • 33 Puccetti L, Pasqui A L, Pastorelli M et al.. Platelet hyperactivity after statin treatment discontinuation.  Thromb Haemost. 2003;  90(3) 476-482
  • 34 Aviram M, Fuhrman B. LDL oxidation by arterial wall macrophages depends on the oxidative status in the lipoprotein and in the cells: role of prooxidants vs. antioxidants.  Mol Cell Biochem. 1998;  188(1-2) 149-159
  • 35 Martinovic I, Abegunewardene N, Seul M et al.. Elevated monocyte chemoattractant protein-1 serum levels in patients at risk for coronary artery disease.  Circ J. 2005;  69(12) 1484-1489
  • 36 Tabata T, Mine S, Kawahara C, Okada Y, Tanaka Y. Monocyte chemoattractant protein-1 induces scavenger receptor expression and monocyte differentiation into foam cells.  Biochem Biophys Res Commun. 2003;  305(2) 380-385
  • 37 Stellos K, Langer H, Daub K et al.. Platelet-derived stromal cell-derived factor-1 regulates adhesion and promotes differentiation of human CD34+ cells to endothelial progenitor cells.  Circulation. 2008;  117(2) 206-215
  • 38 Ma F X, Zhou B, Chen Z et al.. Oxidized low density lipoprotein impairs endothelial progenitor cells by regulation of endothelial nitric oxide synthase.  J Lipid Res. 2006;  47(6) 1227-1237
  • 39 Vainio S, Ikonen E. Macrophage cholesterol transport: a critical player in foam cell formation.  Ann Med. 2003;  35(3) 146-155
  • 40 Keiper T, Al-Fakhri N, Chavakis E et al.. The role of junctional adhesion molecule-C (JAM-C) in oxidized LDL-mediated leukocyte recruitment.  FASEB J. 2005;  19(14) 2078-2080
  • 41 Ostermann G, Fraemohs L, Baltus T et al.. Involvement of JAM-A in mononuclear cell recruitment on inflamed or atherosclerotic endothelium: inhibition by soluble JAM-A.  Arterioscler Thromb Vasc Biol. 2005;  25(4) 729-735
  • 42 Chen T, Febbraio M, Li W, Silverstein R L. A specific CD36 dependent signaling pathway is required for platelet activation by oxidized low-density lipopiotein.  Circ Res. 2008;  102(12) 1512-1519

Stephan LindemannM.D. 

Medizinische Klinik, Abt. III, Kardiologie und Kreislauferkrankungen

Eberhard-Karls-Universität Tübingen, Otfried-Müller-Str.10, D-72076 Tübingen, Germany

Email: Stephan.lindemann@med.uni-tuebingen.de

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