The Novel Oral Syk Inhibitor, Bl1002494, Protects Mice From Arterial Thrombosis and Thromboinflammatory Brain Infarction
Author(s) -
Judith M.M. van Eeuwijk,
David Stegner,
David Lamb,
Peter Kraft,
Sarah Beck,
Ina Thielmann,
Friedemann Kiefer,
Barbara Walzog,
Guido Stoll,
Bernhard Nieswandt
Publication year - 2016
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.115.306883
Subject(s) - syk , gpvi , medicine , thrombosis , stroke (engine) , thrombus , hemostasis , platelet , platelet activation , platelet membrane glycoprotein , receptor , tyrosine kinase , mechanical engineering , engineering
Ischemic stroke, which is mainly caused by thromboembolic occlusion of brain arteries, is the second leading cause of death and disability worldwide with limited treatment options. The platelet collagen receptor glycoprotein VI (GPVI) is a key player in arterial thrombosis and a critical determinant of stroke outcome, making its signaling pathway an attractive target for pharmacological intervention. The spleen tyrosine kinase (Syk) is an essential signaling mediator downstream of not only GPVI but also other platelet and immune cell receptors. We sought to assess whether Syk might be an effective antithrombotic target.
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