Acute and persistent platelet and coagulant activities in atherothrombosis

T. G. Mastenbroek, J. P. Van Geffen, J. W. M. Heemskerk, J. M. E. M. Cosemans*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

The potential relevance of murine atherothrombosis models for understanding human disease has been debated in the past. Despite this, in the last decade, many thrombosis studies with atherogenic Apoe(-/-) mice have been performed, which provide novel insight into the molecular mechanisms by which platelet and coagulation processes accomplish acute thrombus formation after plaque disruption invivo. Support for these mechanisms has come from whole blood flow perfusion studies over plaque material invitro, which are also reviewed in this study. The main plaque-derived triggers for thrombus formation appear to be collagen and tissue factor, next to bioactive mediators such as prostaglandin E2. The atherothrombotic process relies on collagen- and ADP-receptor-induced platelet activation as well as on thrombin/fibrin generation via the extrinsic and intrinsic coagulation pathways. Less is known of the persistent effects of a thrombus on atherosclerosis progression, but evidence suggests roles herein of activated platelets and ongoing thrombin generation.
Original languageEnglish
Pages (from-to)S272-S280
JournalJournal of Thrombosis and Haemostasis
Volume13
DOIs
Publication statusPublished - Jun 2015

Keywords

  • atherosclerotic plaque
  • blood coagulation
  • mouse
  • platelets
  • rupture
  • thrombosis

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