Atherosclerosis has an important inflammatory component. Macrophages accumulating in atherosclerotic arteries produce prostaglandin E(2) (PGE(2)), a main inflammatory mediator. Platelets express inhibitory receptors (EP(2), EP(4)) and a stimulatory receptor (EP(3)) for this prostanoid. Recently, it has been reported in ApoE(-/-) mice that PGE(2) accumulating in inflammatory atherosclerotic lesions might contribute to atherothrombosis after plaque rupture by activating platelet EP(3), and EP(3) blockade has been proposed to be a promising new approach in anti-thrombotic therapy. The aim of our investigation was to study the role of PGE(2) in human atherosclerotic plaques on human platelet function and thrombus formation. Plaque PGE(2) might either activate or inhibit platelets depending on stimulation of either EP(3) or EP(4), respectively. We found that the two EP(3)-antagonists AE5-599 (300 nM) and AE3-240 (300 nM) specifically and completely inhibited the synergistic effect of the EP(3)-agonist sulprostone on U46619-induced platelet aggregation in blood. However, these two EP(3)-antagonists neither inhibited atherosclerotic plaque-induced platelet aggregation, GPIIb/IIIa exposure, dense and alpha granule secretion in blood nor reduced plaque-induced platelet thrombus formation under arterial flow. The EP(4)-antagonist AE3-208 (1-3 μM) potentiated in combination with PGE(2) (1 μM) ADP-induced aggregation, demonstrating that PGE(2) enhances platelet aggregation when the inhibitory EP(4)-receptor is inactivated. However, plaque-induced platelet aggregation was not augmented after platelet pre-treatment with AE3-208, indicating that plaque PGE(2) does not stimulate the EP(4)-receptor. We found that PGE(2) was present in plaques only at very low levels (15 pg PGE(2)/mg plaque). We conclude that PGE(2) in human atherosclerotic lesions does not modulate (i.e. stimulate or inhibit) atherothrombosis in blood after plaque rupture.
Dear Sirs, Acute coronary syndromes, myocardial infarction and ischaemic stroke are leading causes of mortality and morbidity. Atherosclerosis, the basis for these diseases, has an important inflammatory component, and macrophages accumulating in atherosclerotic arteries produce prostaglandin E 2 (PGE 2), a major inflammatory mediator (1-3). Recently, it has been reported in mice that PGE 2 accumulating in inflammatory atherosclerotic lesions might contribute to atherothrombosis after plaque rupture (4). Human platelets express different G-protein coupled receptors for this prostanoid, i.e. EP 2 , EP 4 and at least three isoforms of the EP 3 receptor (5). The main activating PGE 2 receptor of mice platelets is the EP 3 receptor which is coupled to G i and lowers cytosolic cAMP-levels (6, 7). Sulprostone is an EP 3-agonist, and it enhances platelet aggregation induced by different agonists in human washed platelets, platelet-rich plasma (PRP), and whole blood (8-10). Several studies have found a potentiating effect of PGE 2 on platelet aggregation and secretion in PRP stimulated by collagen, ADP and U46619 (8-14). However, in some studies, potentiation of PGE 2 was variable between different blood donors (8, 11, 14). We have examined the effects of PGE 2 in comparison to sulprostone on hirudinised and citrated whole blood by using multiple electrode aggregometry (MEA) (15). Platelet aggregation measured by this method is mediated by binding of fibrinogen to the exposed α IIb β 3 integrin and
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.