Specific binding of hypochlorite-oxidized HDL to platelet CD36 triggers proinflammatory and procoagulant effects

Atherosclerosis. 2010 Sep;212(1):153-60. doi: 10.1016/j.atherosclerosis.2010.05.010. Epub 2010 May 13.

Abstract

Objective: Oxidative stress and systemic inflammation negatively affect several protective functions of high density lipoproteins (HDL) and oxidative modification of HDL by the inflammation-derived oxidant hypochlorite converts HDL into a potent platelet agonist. Therefore it was the aim of this work to clarify if these platelet-activating effects result from specific binding of hypochlorite-oxidized HDL (hyp-OxHDL) to the platelet surface and to identify responsible receptors.

Methods: Binding and functional studies were performed with hyp-OxHDL in absence and presence of (potential) competitors in normal and CD36-deficient human platelets. Platelet aggregation was quantified by light transmission aggregometry. Surface expression of CD62P, phosphatidylserine and CD40L was quantified by flow cytometry.

Results: Binding studies reveal that hyp-OxHDL show specific and saturable high-affinity binding to the platelet surface. Hyp-OxHDL trigger platelet aggregation and in a dose dependent way provoke the release of significant amounts of CD40L as well as phosphatidylserine on the platelet surface. Blocking specific binding of hyp-OxHDL to the platelet surface interferes with the ability of hyp-OxHDL to stimulate human platelets. CD36-deficient human platelets show markedly reduced binding of hyp-OxHDL. Upon addition of hypochlorite-oxidized HDL, CD36-deficient platelets do not aggregate and completely fail to release CD40L or phosphatidylserine.

Conclusions: From these results we conclude that specific binding of hyp-OxHDL to platelet CD36 is essential for the proinflammatory and procoagulant effects of hyp-OxHDL shown within this work. The contribution of other receptors besides CD36 to specific binding of hyp-OxHDL to the platelet membrane appears to be minimal, at best.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding, Competitive
  • Blood Coagulation*
  • Blood Platelets / immunology
  • Blood Platelets / metabolism*
  • CD36 Antigens / blood*
  • CD36 Antigens / deficiency
  • CD40 Ligand / blood
  • Calcium Signaling
  • Flow Cytometry
  • Humans
  • Hypochlorous Acid / chemistry*
  • Inflammation / blood*
  • Inflammation / immunology
  • Inflammation Mediators / blood*
  • Lipoproteins, HDL / blood*
  • Male
  • Oxidants / chemistry*
  • Oxidation-Reduction
  • P-Selectin / blood
  • Phosphatidylserines / blood
  • Platelet Aggregation
  • Platelet Function Tests
  • Protein Binding
  • Reactive Oxygen Species / blood
  • Time Factors

Substances

  • CD36 Antigens
  • Inflammation Mediators
  • Lipoproteins, HDL
  • Oxidants
  • P-Selectin
  • Phosphatidylserines
  • Reactive Oxygen Species
  • CD40 Ligand
  • Hypochlorous Acid