Key result
Targeting glycoprotein VI suppresses thrombosis and thrombo-inflammation without impairing hemostasis.
Why the study?
Novel pharmacological targets for platelet inhibition are needed due to the negative effects of existing antiplatelet drugs on primary hemostasis.
Glycoprotein VI represents a promising novel pharmacological target for platelet inhibition that may prevent thrombosis without the negative effect on primary hemostasis seen with existing antiplatelet drugs.
Coronary artery thrombosis and ischemic stroke are often initiated by the disruption of an atherosclerotic plaque and consequent intravascular platelet activation. Thus, antiplatelet drugs are central in the treatment and prevention of the initial, and subsequent, vascular events. However, novel pharmacological targets for platelet inhibition remain an important goal of cardiovascular research because of the negative effect of existing antiplatelet drugs on primary hemostasis. One promising target is the platelet collagen receptor glycoprotein VI. Blockade or antibody-mediated depletion of this receptor in circulating platelets is beneficial in experimental models of thrombosis and thrombo-inflammatory diseases, such as stroke, without impairing hemostasis. In this review, we summarize the importance of glycoprotein VI and (hem)immunoreceptor tyrosine-based activation motif signaling in hemostasis, thrombosis, and thrombo-inflammatory processes and discuss the targeting strategies currently under development for inhibiting glycoprotein VI and its signaling.
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Stegner et al. (2014) conducted a review in Thrombosis and thrombo-inflammatory diseases. Glycoprotein VI and ITAM signaling pathway targeting was evaluated. Targeting the platelet collagen receptor glycoprotein VI and its signaling pathway is a promising strategy for treating thrombosis and thrombo-inflammatory diseases without impairing hemostasis.
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