Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland, OH (A.A., C.L.J., S.J.C.).
Case Western Reserve University School of Medicine, Cleveland, OH (E.M., S.J.C.).
Circ Res. 2023 Mar 17;132(6):775-790. doi: 10.1161/CIRCRESAHA.122.321566. Epub 2023 Mar 16.
Platelets are small, anucleate entities that bud from megakaryocytes in the bone marrow. Among circulating cells, platelets are the most abundant cell, traditionally involved in regulating the balance between thrombosis (the terminal event of platelet activation) and hemostasis (a protective response to tissue injury). Although platelets lack the precise cellular control offered by nucleate cells, they are in fact very dynamic cells, enriched in preformed RNA that allows them the capability of de novo protein synthesis which alters the platelet phenotype and responses in physiological and pathological events. Antiplatelet medications have significantly reduced the morbidity and mortality for patients afflicted with thrombotic diseases, including stroke and myocardial infarction. However, it has become apparent in the last few years that platelets play a critical role beyond thrombosis and hemostasis. For example, platelet-derived proteins by constitutive and regulated exocytosis can be found in the plasma and may educate distant tissue including blood vessels. First, platelets are enriched in inflammatory and anti-inflammatory molecules that may regulate vascular remodeling. Second, platelet-derived microparticles released into the circulation can be acquired by vascular endothelial cells through the process of endocytosis. Third, platelets are highly enriched in mitochondria that may contribute to the local reactive oxygen species pool and remodel phospholipids in the plasma membrane of blood vessels. Lastly, platelets are enriched in proteins and phosphoproteins which can be secreted independent of stimulation by surface receptor agonists in conditions of disturbed blood flow. This so-called biomechanical platelet activation occurs in regions of pathologically narrowed (atherosclerotic) or dilated (aneurysmal) vessels. Emerging evidence suggests platelets may regulate the process of angiogenesis and blood flow to tumors as well as education of distant organs for the purposes of allograft health following transplantation. This review will illustrate the potential of platelets to remodel blood vessels in various diseases with a focus on the aforementioned mechanisms.
血小板是从骨髓中的巨核细胞中芽生而来的小型无核实体。在循环细胞中,血小板是最丰富的细胞,传统上参与调节血栓形成(血小板激活的终末事件)和止血(对组织损伤的保护性反应)之间的平衡。虽然血小板缺乏有核细胞提供的精确细胞控制,但实际上它们是非常活跃的细胞,富含预先形成的 RNA,使它们能够从头合成蛋白质,从而改变血小板表型和在生理和病理事件中的反应。抗血小板药物显著降低了患有血栓性疾病(包括中风和心肌梗死)的患者的发病率和死亡率。然而,在过去几年中,人们已经清楚地认识到,血小板在血栓形成和止血之外发挥着关键作用。例如,血小板衍生的蛋白质通过组成型和调节型胞吐作用可以在血浆中找到,并可能对包括血管在内的远处组织进行教育。首先,血小板富含炎症和抗炎分子,这些分子可能调节血管重塑。其次,释放到循环中的血小板衍生的微泡可以通过内吞作用被血管内皮细胞摄取。第三,血小板富含线粒体,可能有助于局部活性氧物质池的形成,并重塑血管内皮细胞的质膜中的磷脂。最后,血小板富含蛋白质和磷酸化蛋白质,这些蛋白质可以在血流紊乱的情况下独立于表面受体激动剂的刺激而分泌。这种所谓的生物力学血小板激活发生在病理性狭窄(动脉粥样硬化)或扩张(动脉瘤)的血管区域。新出现的证据表明,血小板可能调节血管生成和肿瘤血流以及移植后同种异体移植物健康的远处器官的教育过程。本综述将说明血小板在各种疾病中重塑血管的潜力,重点介绍上述机制。