Cyclooxygenase-2-derived prostacyclin regulates arterial thrombus formation by suppressing tissue factor in a sirtuin-1-dependent-manner
Articolo
Data di Pubblicazione:
2012
Citazione:
Cyclooxygenase-2-derived prostacyclin regulates arterial thrombus formation by suppressing tissue factor in a sirtuin-1-dependent-manner / S. Barbieri, P. Amadio, S. Gianellini, E. Tarantino, E. Zacchi, F. Veglia, L. Howe, B. Weksler, L. Mussoni, E. Tremoli. - In: CIRCULATION. - ISSN 0009-7322. - 126:11(2012 Sep 11), pp. 1373-1384.
Abstract:
BACKGROUND:
Selective inhibitors of cyclooxygenase (COX)-2 increase the risk of myocardial infarction We found that ferric chloride-induced arterial thrombus formation was significantly and thrombotic events, but the responsible mechanisms are not fully understood.
METHODS AND RESULTS:
greater in COX-2 knockout compared with wild-type mice. Cross-transfusion experiments excluded the likelihood that COX-2 knockout platelets, despite enhanced aggregation responses to collagen and thrombin, are responsible for increased arterial thrombus formation in COX-2 knockout mice. Importantly, we observed that COX-2 deletion decreased prostacyclin synthase and production and peroxisome proliferator-activated receptor- and sirtuin-1 (SIRT1) expression, with consequent increased upregulation of tissue factor (TF), the primary initiator of blood coagulation. Treatment of wild-type mice with a prostacyclin receptor antagonist or a peroxisome proliferator-activated receptor-δ antagonist, which predisposes to arterial thrombosis, decreased SIRT1 expression and increased TF activity. Conversely, exogenous prostacyclin or peroxisome proliferator-activated receptor-δ agonist completely reversed the thrombotic phenotype in COX-2 knockout mice, restoring normal SIRT1 levels and reducing TF activity. Furthermore, inhibition of SIRT1 increased TF expression and activity and promoted generation of occlusive thrombi in wild-type mice, whereas SIRT1 activation was sufficient to decrease abnormal TF activity and prothrombotic status in COX-2 knockout mice.
CONCLUSIONS:
Modulation of SIRT1 and hence TF by prostacyclin/peroxisome proliferator-activated receptor-δ pathways not only represents a new mechanism in controlling arterial thrombus formation but also might be a useful target for therapeutic intervention in the atherothrombotic complications associated with COX-2 inhibitors.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
blood coagulation; carotid arteries; prostacyclin; signal transduction; thrombosis
Elenco autori:
S. Barbieri, P. Amadio, S. Gianellini, E. Tarantino, E. Zacchi, F. Veglia, L. Howe, B. Weksler, L. Mussoni, E. Tremoli
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