Signal-dependent protein synthesis by activated platelets - New pathways to altered phenotype and function

被引:150
作者
Zimmerman, Guy A. [1 ,2 ,3 ]
Weyrich, Andrew S. [1 ,2 ,3 ]
机构
[1] Univ Utah, Sch Med, Eccles Inst Human Genet, Dept Internal Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Sch Med, Eccles Inst Human Genet, Dept Neurobiol Anat, Salt Lake City, UT 84132 USA
[3] Univ Utah, Sch Med, Program Human Mol Biol & Genet, Salt Lake City, UT 84132 USA
关键词
platelets; translation; protein synthesis; transcriptome; proteome; thrombosis;
D O I
10.1161/ATVBAHA.107.160218
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
New biologic activities of platelets continue to be discovered, indicating that concepts of platelet function in hemostasis, thrombosis, and inflammation require reconsideration as new paradigms evolve. Studies done over 3 decades ago demonstrated that mature circulating platelets have protein synthetic capacity, but it was thought to be low level and inconsequential. In contrast, recent discoveries demonstrate that platelets synthesize protein products with important biologic activities in a rapid and sustained fashion in response to cellular activation. This process, termed signal-dependent translation, uses a constitutive transcriptome and specialized pathways, and can alter platelet phenotype and functions in a fashion that can have clinical relevance. Signal-dependent translation and consequent protein synthesis are examples of a diverse group of posttranscriptural mechanisms in activated platelets that are now being revealed.
引用
收藏
页码:S17 / S24
页数:8
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