a Department of Physiology and Pharmacology, Cumming School of Medicine , University of Calgary, and Libin Cardiovascular Institute of Alberta , Calgary , Canada.
Crit Rev Clin Lab Sci. 2017 Nov-Dec;54(7-8):458-470. doi: 10.1080/10408363.2017.1394267. Epub 2017 Oct 30.
As the primary interface between the blood and various tissues of the body, the vascular endothelium exhibits a diverse range of roles and activities, all of which contribute to the overall health and function of the cardiovascular system. In this focused review, we discuss several key aspects of endothelial function, how this may be compromised and subsequent consequences. Specifically, we examine the dynamic regulation of arterial contractility and distribution of blood flow through the generation of chemical and electrical signaling events that impinge upon vascular smooth muscle. The endothelium can generate a diverse range of vasoactive compounds and signals, most of which act locally to adjust blood flow in a dynamic fashion to match tissue metabolism. Disruption of these vascular signaling processes (e.g. reduced nitric oxide bioavailability) is typically referred to as endothelial dysfunction, which is a recognized risk factor for cardiovascular disease in patients and occurs early in the development and progression of hypertension, atherosclerosis and tissue ischemia. Endothelial dysfunction is also associated with type-2 Diabetes and aging and increased mechanistic knowledge of the cellular changes contributing to these effects may provide important clues for interventional strategies. The endothelium also serves as the initial site of interaction for immune cells entering tissues in response to damage and acts to facilitate the actions of both the innate and acquired immune systems to interact with the vascular wall. In addition to representing the main cell type responsible for the formation of new blood vessels (i.e. angiogenesis) within the vasculature, the endothelium is also emerging as a source of extracellular vesicle or microparticles for the transport of signaling molecules and other cellular materials to nearby, or remote, sites in the body. The characteristics of released microparticles appear to change with the functional status of the endothelium; thus, these microparticles may represent novel biomarkers of endothelial health and more serious cardiovascular disease.
作为血液与体内各种组织之间的主要界面,血管内皮表现出多样化的作用和活动,所有这些都有助于心血管系统的整体健康和功能。在本次重点综述中,我们讨论了内皮功能的几个关键方面,包括内皮功能如何受损以及随后的后果。具体来说,我们研究了动脉收缩性的动态调节以及通过产生影响血管平滑肌的化学和电信号事件来分配血流。内皮可以产生多种血管活性化合物和信号,其中大多数局部作用是根据组织代谢以动态方式调节血流。这些血管信号过程的破坏(例如,一氧化氮生物利用度降低)通常被称为内皮功能障碍,这是患者心血管疾病的公认危险因素,并且发生在高血压、动脉粥样硬化和组织缺血的发展和进展的早期。内皮功能障碍也与 2 型糖尿病和衰老有关,对导致这些效应的细胞变化的机制知识的增加可能为干预策略提供重要线索。内皮也是免疫细胞进入组织以响应损伤的初始相互作用部位,并作用于先天和获得性免疫系统以与血管壁相互作用。内皮不仅代表了血管内形成新血管(即血管生成)的主要细胞类型,而且还作为细胞外囊泡或微颗粒的来源,用于将信号分子和其他细胞物质运输到身体的附近或远处部位。释放的微颗粒的特征似乎随内皮功能的状态而变化;因此,这些微颗粒可能代表内皮健康和更严重心血管疾病的新型生物标志物。