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PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways

Platelet endothelial cell adhesion molecule-1 (PECAM-1) inhibits platelet response to collagen and may also inhibit two other major platelet agonists ADP and thrombin although this has been less well explored. We hypothesized that the combined effect of inhibiting these three platelet activating pat...

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Autores principales: Jones, Chris I., Garner, Stephen F., Moraes, Leonardo A., Kaiser, William J., Rankin, Angela, Ouwehand, Willem H., Goodall, Alison H., Gibbins, Jonathan M.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2791847/
https://www.ncbi.nlm.nih.gov/pubmed/19850043
http://dx.doi.org/10.1016/j.febslet.2009.10.037
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author Jones, Chris I.
Garner, Stephen F.
Moraes, Leonardo A.
Kaiser, William J.
Rankin, Angela
Ouwehand, Willem H.
Goodall, Alison H.
Gibbins, Jonathan M.
author_facet Jones, Chris I.
Garner, Stephen F.
Moraes, Leonardo A.
Kaiser, William J.
Rankin, Angela
Ouwehand, Willem H.
Goodall, Alison H.
Gibbins, Jonathan M.
author_sort Jones, Chris I.
collection PubMed
description Platelet endothelial cell adhesion molecule-1 (PECAM-1) inhibits platelet response to collagen and may also inhibit two other major platelet agonists ADP and thrombin although this has been less well explored. We hypothesized that the combined effect of inhibiting these three platelet activating pathways may act to significantly inhibit thrombus formation. We demonstrate a negative relationship between PECAM-1 surface expression and platelet response to cross-linked collagen related peptide (CRP-XL) and ADP, and an inhibitory effect of PECAM-1 clustering on platelet response to CRP-XL, ADP and thrombin. This combined inhibition of multiple signaling pathways results in a marked reduction in thrombus formation.
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spelling pubmed-27918472009-12-22 PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways Jones, Chris I. Garner, Stephen F. Moraes, Leonardo A. Kaiser, William J. Rankin, Angela Ouwehand, Willem H. Goodall, Alison H. Gibbins, Jonathan M. FEBS Lett Article Platelet endothelial cell adhesion molecule-1 (PECAM-1) inhibits platelet response to collagen and may also inhibit two other major platelet agonists ADP and thrombin although this has been less well explored. We hypothesized that the combined effect of inhibiting these three platelet activating pathways may act to significantly inhibit thrombus formation. We demonstrate a negative relationship between PECAM-1 surface expression and platelet response to cross-linked collagen related peptide (CRP-XL) and ADP, and an inhibitory effect of PECAM-1 clustering on platelet response to CRP-XL, ADP and thrombin. This combined inhibition of multiple signaling pathways results in a marked reduction in thrombus formation. Elsevier Science B.V 2009-11-19 /pmc/articles/PMC2791847/ /pubmed/19850043 http://dx.doi.org/10.1016/j.febslet.2009.10.037 Text en © 2009 Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Jones, Chris I.
Garner, Stephen F.
Moraes, Leonardo A.
Kaiser, William J.
Rankin, Angela
Ouwehand, Willem H.
Goodall, Alison H.
Gibbins, Jonathan M.
PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways
title PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways
title_full PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways
title_fullStr PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways
title_full_unstemmed PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways
title_short PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways
title_sort pecam-1 expression and activity negatively regulate multiple platelet signaling pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2791847/
https://www.ncbi.nlm.nih.gov/pubmed/19850043
http://dx.doi.org/10.1016/j.febslet.2009.10.037
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