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Author Notes:

Correspondence: Lawrence F. Brass, University of Pennsylvania, 915 BRB II/III, 421 Curie Blvd, Philadelphia, PA 19104, USA. Tel.: +1 215–573–3540; fax: +1 215–573–7039. brass@mail.med.upenn.edu.

T.J. Stalker designed and performed experiments, analyzed data and wrote the paper; J. Wu, A. Morgans, E.A. Traxler, L. Wang, M.S. Chatterjee and D. Lee performed experiments and analyzed data; T. Quertermous, R.A. Hall, D.A. Hammer and S.L. Diamond provided vital analytical tools; L.F. Brass designed experiments, analyzed data and wrote the paper.

The authors state that they have no conflict of interest.


Research Funding:

These studies were supported by grant numbers P01-HL040387 (L.F. Brass) and R33-HL087317 (D.A. Hammer, S.L. Diamond and L.F. Brass) from the National Heart, Lung and Blood Institute.

T.J. Stalker was supported by American Heart Association post-doctoral fellowship 0525630U.


  • Science & Technology
  • Life Sciences & Biomedicine
  • Hematology
  • Peripheral Vascular Disease
  • Cardiovascular System & Cardiology
  • ESAM
  • NHERF-1
  • PDZ domain
  • platelets
  • thrombosis

Endothelial cell specific adhesion molecule (ESAM) localizes to platelet-platelet contacts and regulates thrombus formation in vivo

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Journal Title:

Journal of Thrombosis and Haemostasis


Volume 7, Number 11


, Pages 1886-1896

Type of Work:

Article | Post-print: After Peer Review


Background: In resting platelets, endothelial cell specific adhesion molecule (ESAM) is located in alpha granules, increasing its cell surface expression following platelet activation. However, the function of ESAM on platelets is unknown. Objective: To determine whether ESAM has a role in thrombus formation. Methods and results: We found that following platelet activation ESAM localizes to the junctions between adjacent platelets, suggesting a role for this protein in contact-dependent events that regulate thrombus formation. To test this hypothesis we examined the effect of ESAM deletion on platelet function. In vivo, ESAM-/- mice achieved more stable hemostasis than wild-type mice following tail transection, and developed larger thrombi following laser injury of cremaster muscle arterioles. In vitro, ESAM-/- platelets aggregated at lower concentrations of G protein-dependent agonists than wild-type platelets, and were more resistant to disaggregation. In contrast, agonist-induced calcium mobilization, αIIbβ3 activation, alpha-granule secretion and platelet spreading, were normal in ESAM-deficient platelets. To understand the molecular mechanism by which ESAM regulates platelet activity, we utilized a PDZ domain array to identify the scaffold protein NHERF-1 as an ESAM binding protein, and further demonstrated that it associates with ESAM in both resting and activated platelets. Conclusions: These findings support a model in which ESAM localizes to platelet contacts following platelet activation in order to limit thrombus growth and stability so that the optimal hemostatic response occurs following vascular injury.

Copyright information:

© 2009 International Society on Thrombosis and Haemostasis.

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