Sulfatides inhibit platelet adhesion to von Willebrand factor in flowing blood

J Thromb Haemost. 2003 Jun;1(6):1288-95. doi: 10.1046/j.1538-7836.2003.00156.x.

Abstract

Sulfatides are sulfated glycosphingolipids present on cell surfaces that bind to adhesive proteins such as von Willebrand factor (VWF), P-selectin, laminin and thrombospondin. Previous studies have localized the sulfatide-binding site of VWF to amino acid residues Gln626-Val646 in the A1 domain. The A1 domain also contains the binding site for platelet glycoprotein Ib (GP Ib), a site that has been reported to be distinct from the sulfatide-binding site. In this study, we analyzed the interaction of sulfatides with VWF and its effect on GP Ib-mediated platelet adhesion under flow conditions. Recombinant VWF A1 domain (rVWF-A1) bound specifically and saturably to sulfatides (half-maximal concentration of approximately 12.5 microg mL(-1)), binding that was blocked by dextran sulfate (IC(50) approximately equal to 100 microg mL(-1)) but not by heparin at concentrations up to 100 U mL(-1). Furthermore, sulfatides (125 microg mL(-1)) prevented the adhesion of platelets or glycocalicin-coupled polystyrene beads to a rVWF-A1-coated surface under high shear stress. In addition, plasma VWF prebound to a sulfatide-coated surface failed to support subsequent platelet adhesion. These results provide firm evidence that sulfatides bind the VWF A1 domain at a site overlapping the GP Ib-binding site.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cloning, Molecular
  • Humans
  • Kinetics
  • Perfusion
  • Platelet Adhesiveness / drug effects*
  • Platelet Glycoprotein GPIb-IX Complex / metabolism
  • Protein Binding / drug effects
  • Recombinant Proteins / metabolism
  • Sulfoglycosphingolipids / pharmacology*
  • Surface Plasmon Resonance
  • von Willebrand Factor / metabolism*

Substances

  • Platelet Glycoprotein GPIb-IX Complex
  • Recombinant Proteins
  • Sulfoglycosphingolipids
  • glycocalicin
  • von Willebrand Factor