PPAR beta/delta Agonists Modulate Platelet Function via a Mechanism Involving PPAR Receptors and Specific Association/Repression of PKC alpha-Brief Report

Détails

ID Serval
serval:BIB_D41B87AC2474
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
PPAR beta/delta Agonists Modulate Platelet Function via a Mechanism Involving PPAR Receptors and Specific Association/Repression of PKC alpha-Brief Report
Périodique
Arteriosclerosis Thrombosis and Vascular Biology
Auteur⸱e⸱s
Ali F.Y., Hall M.G., Desvergne B., Warner T.D., Mitchell J.A.
ISSN
1079-5642
Statut éditorial
Publié
Date de publication
2009
Peer-reviewed
Oui
Volume
29
Numéro
11
Pages
1871-1873
Langue
anglais
Résumé
Objectives-Peroxisome proliferator-activated receptor beta/delta (PPAR beta/delta) is a nuclear receptor found in platelets. PPAR beta/delta agonists acutely inhibit platelet function within a few minutes of addition. As platelets are anucleated, the effects of PPAR beta/delta agonists on platelets must be nongenomic. Currently, the particular role of PPAR beta/delta receptors and their intracellular signaling pathways in platelets are not known.
Methods and Results-We have used mice lacking PPAR beta/delta (PPAR beta/delta(-/-)) to show the effects of the PPAR beta/delta agonist GW501516 on platelet adhesion and cAMP levels are mediated specifically by PPAR beta/delta, however GW501516 had no PPAR beta/delta-specific effect on platelet aggregation. Studies in human platelets showed that PKC alpha, which can mediate platelet activation, was bound and repressed by PPAR beta/delta after platelets were treated with GW501516.
Conclusions-These data provide evidence of a novel mechanism by which PPAR receptors influence platelet activity and thereby thrombotic risk. (Arterioscler Thromb Vasc Biol. 2009; 29: 1871-1873.)
Mots-clé
Platelets, PPAR beta/delta, PKC alpha, Knockout mice, Protein-Kinase-C, Fibroblasts
Web of science
Open Access
Oui
Création de la notice
04/11/2009 14:16
Dernière modification de la notice
20/08/2019 15:54
Données d'usage