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A dual thrombin receptor system for platelet activation.

Platelet-dependent arterial thrombosis triggers most heart attacks and strokes. Because the coagulation protease thrombin is the most potent activator of platelets, identification of the platelet receptors for thrombin is critical for understanding thrombosis and haemostasis. Protease-activated receptor-1 (PAR1) is important for activation of human platelets by thrombin, but plays no apparent role in mouse platelet activation. PAR3 is a thrombin receptor that is expressed in mouse megakaryocytes. Here we report that thrombin responses in platelets from PAR3-deficient mice were markedly delayed and diminished but not absent. We have also identified PAR4, a new thrombin-activated receptor. PAR4 messenger RNA was detected in mouse megakaryocytes and a PAR4-activating peptide caused secretion and aggregation of PAR3-deficient mouse platelets. Thus PAR3 is necessary for normal thrombin responses in mouse platelets, but a second PAR4-mediated mechanism for thrombin signalling exists. Studies with PAR-activating peptides suggest that PAR4 also functions in human platelets, which implies that an analogous dual-receptor system also operates in humans. The identification of a two-receptor system for platelet activation by thrombin has important implications for the development of antithrombotic therapies.

Pubmed ID: 9716134

Authors

  • Kahn ML
  • Zheng YW
  • Huang W
  • Bigornia V
  • Zeng D
  • Moff S
  • Farese RV
  • Tam C
  • Coughlin SR

Journal

Nature

Publication Data

August 13, 1998

Associated Grants

None

Mesh Terms

  • Amino Acid Sequence
  • Animals
  • Cells, Cultured
  • Cloning, Molecular
  • Female
  • Gene Targeting
  • Humans
  • Ligands
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Peptides
  • Platelet Activation
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, Thrombin
  • Signal Transduction
  • Thrombin
  • Xenopus