Wu K K, Thiagarajan P
Department of Internal Medicine, University of Texas-Houston Medical School 77030, USA.
Annu Rev Med. 1996;47:315-31. doi: 10.1146/annurev.med.47.1.315.
Vascular endothelium is strategically located at the interface between tissue and blood. It is pivotal for protecting against vascular injury and maintaining blood fluidity. Normal endothelium releases prostacyclin and nitric oxide, potent inhibitors of platelet and monocyte activation and vasodilators. Their syntheses are governed by isoforms of enzymes. Normal endothelial surface expresses ecto-adenosine diphosphatase, which degrades adenosine diphosphate and inhibits platelet aggregation; thrombomodulin, which serves as a binding site for thrombin to activate protein C; and heparin-like molecules, which serve as a cofactor for antithrombin III. Normal endothelium secretes tissue plasminogen activator, which activates the fibrinolysis system. Endothelium produces and secretes von Willebrand factor, which mediates platelet adhesion and shear-stress-induced aggregation. Injury to endothelium is accompanied by loss of protective molecules and expression of adhesive molecules, procoagulant activities, and mitogenic factors, leading to development of thrombosis, smooth muscle cell migration, and proliferation and atherosclerosis.
血管内皮位于组织与血液的界面处,具有重要的战略地位。它对于预防血管损伤和维持血液流动性至关重要。正常内皮会释放前列环素和一氧化氮,这两种物质是血小板和单核细胞活化的强效抑制剂以及血管舒张剂。它们的合成由酶的同工型控制。正常内皮表面表达外切腺苷二磷酸酶,该酶可降解二磷酸腺苷并抑制血小板聚集;血栓调节蛋白,它作为凝血酶激活蛋白C的结合位点;以及类肝素分子,其作为抗凝血酶III的辅因子。正常内皮会分泌组织型纤溶酶原激活剂,从而激活纤维蛋白溶解系统。内皮产生并分泌血管性血友病因子,该因子介导血小板黏附和剪切应力诱导的聚集。内皮损伤伴随着保护性分子的丧失以及黏附分子、促凝血活性和有丝分裂因子的表达,进而导致血栓形成、平滑肌细胞迁移、增殖以及动脉粥样硬化的发展。