Thrombospondin-1 stimulates platelet aggregation by blocking the antithrombotic activity of nitric oxide/cGMP signaling

Blood. 2008 Jan 15;111(2):613-23. doi: 10.1182/blood-2007-06-098392. Epub 2007 Sep 21.

Abstract

Platelet alpha-granules constitute the major rapidly releasable reservoir of thrombospondin-1 in higher animals. Although some fragments and peptides derived from thrombospondin-1 stimulate or inhibit platelet aggregation, its physiologic function in platelets has remained elusive. We now show that endogenous thrombospondin-1 is necessary for platelet aggregation in vitro in the presence of physiologic levels of nitric oxide (NO). Exogenous NO or elevation of cGMP delays thrombin-induced platelet aggregation under high shear and static conditions, and exogenous thrombospondin-1 reverses this delay. Thrombospondin-1-null murine platelets fail to aggregate in response to thrombin in the presence of exogenous NO or 8Br-cGMP. At physiologic concentrations of the NO synthase substrate arginine, thrombospondin-1-null platelets have elevated basal cGMP. Ligation of CD36 or CD47 is sufficient to block NO-induced cGMP accumulation and mimic the effect of thrombospondin-1 on aggregation. Exogenous thrombospondin-1 also reverses the suppression by NO of alphaIIb/beta3 integrin-mediated platelet adhesion on immobilized fibrinogen, mediated in part by increased GTP loading of Rap1. Thrombospondin-1 also inhibits cGMP-mediated activation of cGMP-dependent protein kinase and thereby prevents phosphorylation of VASP. Thus, release of thrombospondin-1 from alpha-granules during activation provides positive feedback to promote efficient platelet aggregation and adhesion by overcoming the antithrombotic activity of physiologic NO.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Arginine / genetics
  • Arginine / metabolism
  • Blood Platelets / cytology
  • Blood Platelets / metabolism*
  • CD36 Antigens / genetics
  • CD36 Antigens / metabolism
  • CD47 Antigen / genetics
  • CD47 Antigen / metabolism
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Cyclic GMP / antagonists & inhibitors
  • Cyclic GMP / genetics
  • Cyclic GMP / metabolism*
  • Cyclic GMP / pharmacology
  • Fibrinolytic Agents / metabolism*
  • Fibrinolytic Agents / pharmacology
  • Immunologic Capping / drug effects
  • Immunologic Capping / physiology
  • Mice
  • Mice, Knockout
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism
  • Nitric Oxide / antagonists & inhibitors
  • Nitric Oxide / genetics
  • Nitric Oxide / metabolism*
  • Peptides / genetics
  • Peptides / metabolism
  • Peptides / pharmacology
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Platelet Adhesiveness / drug effects
  • Platelet Adhesiveness / genetics
  • Platelet Aggregation / drug effects
  • Platelet Aggregation / physiology*
  • Platelet Glycoprotein GPIIb-IIIa Complex / genetics
  • Platelet Glycoprotein GPIIb-IIIa Complex / metabolism
  • Secretory Vesicles / genetics
  • Secretory Vesicles / metabolism
  • Shear Strength
  • Thrombin / genetics
  • Thrombin / metabolism
  • Thrombin / pharmacology
  • Thrombospondin 1 / genetics
  • Thrombospondin 1 / metabolism*
  • Thrombospondin 1 / pharmacology
  • rap1 GTP-Binding Proteins / genetics
  • rap1 GTP-Binding Proteins / metabolism

Substances

  • CD36 Antigens
  • CD47 Antigen
  • Cd47 protein, mouse
  • Cell Adhesion Molecules
  • Fibrinolytic Agents
  • Microfilament Proteins
  • Peptides
  • Phosphoproteins
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Thrombospondin 1
  • vasodilator-stimulated phosphoprotein
  • Nitric Oxide
  • Arginine
  • Thrombin
  • rap1 GTP-Binding Proteins
  • Cyclic GMP