Integrin αIIbβ3 and Its Antagonism

• Published in: Arteriosclerosis, thrombosis, and vascular biology Vol. 23; no. 6; pp. 945 - 952
• Main Authors: Quinn, Martin J, Byzova, Tatiana V, Qin, Jun, Topol, Eric J, Plow, Edward F
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Heart Association, Inc 01.06.2003; Hagerstown, MD Lippincott
• Subjects: Biological and medical sciences; Blood coagulation; Investigative techniques, diagnostic techniques (general aspects); Medical sciences; Human; Membrane protein; platelet function inhibitors; Ligand; Coagulation; Exploration; Activation; aggregation; Biological activity; acute coronary syndromes; platelets; Antagonism; Platelet; Integrin; Structural analysis
• ISSN: 1079-5642; 1524-4636
• DOI: 10.1161/01.ATV.0000066686.46338.F1

αIIbβ3, the major membrane protein on the surface of platelets, is a member of the integrin family of heterodimeric adhesion receptors. The αIIb and β3 subunits are each composed of a short cytoplasmic tail, a single transmembrane domain, and a large, extracellular region that consists of a series of linked domains. Recent structural analyses have provided insights into the organization of this and other integrins and how a signal is initiated at its cytoplasmic tail to transform the extracellular domain of αIIbβ3 into a functional receptor for fibrinogen or von Willebrand factor to support platelet aggregation and thrombus formation. These functions of αIIbβ3 have been targeted for antithrombotic therapy, and intravenous αIIbβ3 antagonists have been remarkably effective in the setting of percutaneous coronary interventions, showing both short-term and long-term mortality benefits. However, the development of oral antagonists has been abandoned on the basis of excess of mortality in clinical trials, and the extension of therapy with existing αIIbβ3 antagonists to broadly treat acute coronary syndromes has not fully met expectations. An in-depth understanding of how antagonists engage and influence the function of αIIbβ3 and platelets in the context of the new structural insights may explain its salutary and potential deleterious effects.