Vajen T, Mause S F, Koenen R R
Rory R. Koenen, PhD, Department of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands, Tel.: +31 43 3881674, Fax: +31 43 3884159, E-mail:
Thromb Haemost. 2015 Aug;114(2):228-36. doi: 10.1160/TH14-11-0962. Epub 2015 May 21.
Microvesicles are receiving increased attention not only as biomarkers but also as mediators of cell communication and as integral effectors of disease. Platelets present a major source of microvesicles and release these microvesicles either spontaneously or upon activation. Platelet-derived microvesicles retain many features of their parent cells and have been shown to exert modulatory effects on vascular and immune cells. Accordingly, microvesicles from platelets can be measured at increased levels in patients with cardiovascular disease or individuals at risk. In addition, isolated microvesicles from platelets were shown to exert immunomodulatory actions on various cell types. In this review the various aspects of platelet-derived microvesicles including release, clearance, measurement, occurrence during disease and relevance for the pathophysiology of vascular inflammation will be discussed.
微泡不仅作为生物标志物,而且作为细胞通讯的介质和疾病的整体效应物,正受到越来越多的关注。血小板是微泡的主要来源,可自发或在激活后释放这些微泡。血小板衍生的微泡保留了其母细胞的许多特征,并已显示出对血管和免疫细胞具有调节作用。因此,心血管疾病患者或有风险的个体中,血小板来源的微泡水平会升高。此外,从血小板中分离出的微泡对多种细胞类型具有免疫调节作用。在这篇综述中,将讨论血小板衍生微泡的各个方面,包括释放、清除、测量、疾病期间的出现情况以及与血管炎症病理生理学的相关性。