Platelet proteomics: from discovery to diagnosis

被引:20
作者
Loosse, Christina [1 ]
Swieringa, Frauke [1 ]
Heemskerk, Johan W. M. [2 ]
Sickmann, Albert [1 ,3 ,4 ]
Lorenz, Christin [1 ]
机构
[1] Leibniz Inst Analyt Wissensch ISAS eV, Bunsen Kirchhoff Str 11, D-44139 Dortmund, Germany
[2] Maastricht Univ, Dept Biochem, CARIM, Maastricht, Netherlands
[3] Ruhr Univ Bochum, Med Fak, Med Proteom Ctr, Bochum, Germany
[4] Univ Aberdeen, Coll Phys Sci, Dept Chem, Aberdeen, Scotland
关键词
Cardiovascular disease; hemostasis; mass spectrometry; platelets; proteomics; quantification; ELEVATION MYOCARDIAL-INFARCTION; THROMBUS FORMATION; ACTIVATED PLATELETS; MASS-SPECTROMETRY; PROTEIN QUANTITATION; O-GLYCOSYLATION; GLOBAL PROTEOME; SCOTT SYNDROME; IN-VIVO; REVEALS;
D O I
10.1080/14789450.2018.1480111
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Platelets are the smallest cells within the circulating blood with key roles in physiological hemostasis and pathological thrombosis regulated by the onset of activating/inhibiting processes via receptor responses and signaling cascades.Areas covered: Proteomics as well as genomic approaches have been fundamental in identifying and quantifying potential targets for future diagnostic strategies in the prevention of bleeding and thrombosis, and uncovering the complexity of platelet functions in health and disease. In this article, we provide a critical overview on current functional tests used in diagnostics and the future perspectives for platelet proteomics in clinical applications.Expert commentary: Proteomics represents a valuable tool for the identification of patients with diverse platelet associated defects. In-depth validation of identified biomarkers, e.g. receptors, signaling proteins, post-translational modifications, in large cohorts is decisive for translation into routine clinical diagnostics.
引用
收藏
页码:467 / 476
页数:10
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