Dynamic microvesicle release and clearance within the cardiovascular system: triggers and mechanisms

被引:51
作者
Ayers, Lisa [1 ,2 ]
Nieuwland, Rienk [3 ]
Kohler, Malcolm [4 ,5 ]
Kraenkel, Nicolle [6 ]
Ferry, Berne [2 ]
Leeson, Paul [1 ]
机构
[1] Univ Oxford, Oxford Cardiovasc Clin Res Facil, Oxford OX3 9DU, England
[2] Oxford Univ Hosp NHS Trust, Dept Clin & Lab Immunol, Oxford OX3 7LE, England
[3] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Zurich Hosp, Dept Pulmonol, CH-8091 Zurich, Switzerland
[5] Univ Zurich, CH-8091 Zurich, Switzerland
[6] Charite, Div Cardiol, Campus Benjamin Franklin, D-10117 Berlin, Germany
基金
美国国家卫生研究院;
关键词
cardiovascular disease; clinical studies; microparticles; microvesicles; PLATELET-DERIVED MICROPARTICLES; CIRCULATING ENDOTHELIAL MICROPARTICLES; CORONARY-HEART-DISEASE; HIGH-SHEAR-STRESS; HIGH-FAT MEAL; TISSUE FACTOR; THROMBIN GENERATION; CYTOKINE PRODUCTION; IN-VITRO; PROCOAGULANT MICROPARTICLES;
D O I
10.1042/CS20140623
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Interest in cell-derived microvesicles (or microparticles) within cardiovascular diagnostics and therapeutics is rapidly growing. Microvesicles are often measured in the circulation at a single time point. However, it is becoming clear that microvesicle levels both increase and decrease rapidly in response to certain stimuli such as hypoxia, acute cardiac stress, shear stress, hypertriglyceridaemia and inflammation. Consequently, the levels of circulating microvesicles will reflect the balance between dynamic mechanisms for release and clearance. The present review describes the range of triggers currently known to lead to microvesicle release from different cellular origins into the circulation. Specifically, the published data are used to summarize the dynamic impact of these triggers on the degree and rate of microvesicle release. Secondly, a summary of the current understanding of microvesicle clearance via different cellular systems, including the endothelial cell and macrophage, is presented, based on reported studies of clearance in experimental models and clinical scenarios, such as transfusion or cardiac stress. Together, this information can be used to provide insights into potential underlying biological mechanisms that might explain the increases or decreases in circulating microvesicle levels that have been reported and help to design future clinical studies.
引用
收藏
页码:915 / 931
页数:17
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