A mechanism to safeguard platelet adhesion under high shear flow: Von Willebrand factor-glycoprotein Ib and integrin α2 β1-collagen interactions make complementary, collagen-type-specific contributions to adhesion

Abstract

Background: Blood vessels contain different types of collagen, with types I and III being the major components of vascular collagen. Platelet adhesion under high shear stress has been suggested to depend on the binding of von Willebrand factor (VWF) to collagen. Objective: We analyzed the collagen type specificity for the interaction with VWF and high shear stress platelet adhesion. Methods: VWF binding to different types of immobilized collagen and effects of antibodies against glycoprotein Ib (gpIb) and integrin α2β1 on platelet adhesion to type I and III collagens under high shear were analyzed. Results: VWF showed high-affinity, selective binding to human and bovine type III collagens, but weak or no affinity for types I, II, IV and V under static conditions. Anti-integrin α2 β1 markedly inhibited adhesion to type I collagen, but did not affect that to type III collagen. Anti-gpIb antibody significantly inhibited adhesion to type III collagen. Adding both antibodies abrogated the adhesion to either type I or III collagen. Conclusions: Both the gpIb-VWF interaction and the integrin α2β1-collagen interaction contribute to platelet adhesion to collagen under high shear stress, and integrin αIIβ1 makes a greater contribution to adhesion to type I collagen because less VWF is bound to it. © 2007 International Society on Thrombosis and Haemostasis.