Montrucchio G, Emanuelli G, Venco A, Camussi G
Dipartimento di Fisiopatologia Clinica, Università degli Studi di Torino.
Ann Ital Med Int. 1995 Jan-Mar;10(1):31-40.
The aim of this review is to summarize the current concepts concerning the active role of the endothelium in the pathogenesis of atherosclerosis. Activated endothelium may promote the adhesion of monocytes and their transmigration into the intima. The coordinated expression of adhesion molecules of the selectin, integrin or immunoglobulin superfamily on the surface of endothelial cells and of monocytes modulates these events. The role of lipoproteins and their oxidative derivatives as well as that of selected cytokines and platelet activated factor in initiating changes on the endothelial cell surface has been investigated: these events are associated with an increased endothelial permeability to lipids and lipoproteins with their accumulation in the subendothelium. Once migrated into the intima, monocytes undergo morphological and functional modifications leading to the generation of a polypeptide mediator network which is instrumental in the migration, differentiation and proliferation of smooth muscle cells. Mediators produced by macrophages infiltrating the atherosclerotic plaque and by the endothelium may render the surface of the endothelial cells thrombogenic thus favoring thrombotic occlusion. In conclusion, the most recent studies suggest that the endothelium plays an active role in the pathogenesis of atherosclerosis.
本综述的目的是总结当前关于内皮细胞在动脉粥样硬化发病机制中的积极作用的相关概念。活化的内皮细胞可促进单核细胞的黏附及其向内皮下的迁移。内皮细胞和单核细胞表面选择素、整合素或免疫球蛋白超家族黏附分子的协同表达调节这些过程。脂蛋白及其氧化衍生物以及某些细胞因子和血小板活化因子在内皮细胞表面引发变化中的作用已得到研究:这些过程与内皮细胞对脂质和脂蛋白的通透性增加及其在血管内膜下的积聚有关。一旦单核细胞迁移到内膜,它们会经历形态和功能的改变,从而导致一个多肽介质网络的产生,该网络有助于平滑肌细胞的迁移、分化和增殖。浸润动脉粥样硬化斑块的巨噬细胞和内皮细胞产生的介质可能使内皮细胞表面具有血栓形成性,从而有利于血栓闭塞。总之,最新研究表明内皮细胞在动脉粥样硬化的发病机制中起积极作用。