Platelet Signaling Pathways and New Inhibitors

被引:43
作者
Grover, Steven P. [1 ]
Bergmeier, Wolfgang [2 ,3 ]
Mackman, Nigel [1 ]
机构
[1] Univ North Carolina Chapel Hill, Dept Med, Div Hematol & Oncol, Thrombosis & Hemostasis Program, Chapel Hill, NC USA
[2] Univ North Carolina Chapel Hill, McAllister Heart Inst, Chapel Hill, NC USA
[3] Univ North Carolina Chapel Hill, Dept Biochem & Biophys, Chapel Hill, NC USA
关键词
hemostasis; myocardial infarction; platelet activation; stroke; thrombosis; CLASS-III PI3K; ARTERIAL THROMBOSIS; PHOSPHATIDYLSERINE EXPOSURE; GLYCOPROTEIN VI; PROTECTS MICE; NADPH-OXIDASE; TRPM7; CHANNEL; EX-VIVO; RECEPTOR; ACTIVATION;
D O I
10.1161/ATVBAHA.118.310224
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent studies have revealed a series of novel mechanisms that either positively or negatively regulate signaling events downstream of receptor-mediated platelet activation. In several cases, it seems that disruption of these pathways can selectively inhibit thrombosis while leaving essential hemostatic processes largely intact. These pathways may be of considerable interest as potential targets for development of a new generation of antiplatelet agents. Other work has focused on the development of novel antiplatelet agents that inhibit established targets such as P2Y12, PAR1, and GPVI. These agents may overcome some of the limitations of established therapies. It remains to be determined if these novel agents will find clinical use. © 2018 American Heart Association, Inc.
引用
收藏
页码:e28 / e35
页数:8
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