What can we learn from senescent platelets, their transcriptomes and proteomes?

被引:5
|
作者
Allan, Harriet E. [1 ]
Vadgama, Ami [1 ]
Armstrong, Paul C. [1 ]
Warner, Timothy D. [1 ,2 ]
机构
[1] Queen Mary Univ London, Blizard Inst, Ctr Immunobiol, London, England
[2] Queen Mary Univ London, Blizard Inst, Ctr Immunobiol, 4 Newark St, London E1 2AT, England
关键词
Platelet aging; reticulated platelets; senescence; RETICULATED PLATELETS; PROTEIN-SYNTHESIS; FRACTION; SIZE; TURNOVER; AGE;
D O I
10.1080/09537104.2023.2200838
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Research into the natural aging process of platelets has garnered much research interest in recent years, and there have long been associations drawn between the proportion of newly formed platelets in the circulation and the risk of thrombosis. However, these observations have largely been demonstrated in patient groups in which there may be underlying systemic changes that effect platelet function. Recent advances in technology have allowed in-depth analysis of differently aged platelets isolated from the peripheral blood of healthy individuals and have demonstrated that aged platelets, often referred to as senescent platelets, undergo extensive changes in the transcriptome and proteome. Ultimately, these changes result in platelets whose functions have deteriorated such that they cannot partake in hemostatic responses to the same extent as newly formed platelets. Here, we review transcriptomic and proteomic research in platelet aging in the context of health and how this research sheds light upon alterations in platelet structure and function.
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收藏
页数:7
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