Mason R G, Sharp D, Chuang H Y, Mohammad S F
Arch Pathol Lab Med. 1977 Feb;101(2):61-4.
The renewed interest in endothelial function is based partly on success with tissue culture of endothelial cells. Endothelium functions primarily in the control of blood vessel wall permeability and in the provision of a blood-compatible lining surface. Recent findings indicate that endothelial cells are active metabolically in ways that may help prevent thrombosis. Endothelium actively degrades several different vasoactive compounds that circulate in blood and that can serve as platelet-aggregating agents. Endothelium also contains an inhibitor of platelet function and an activator of plasminogen, both of which can be released from the cell in response to appropriate stimuli. While intact endothelium functions primarily in prevention of thrombosis, damaged endothelium can contribute greatly to thrombus formation. Release of prostaglandins, adenine nucleotides, and other intracellular components from damaged endothelium can enhance platelet aggregation. Damaged endothelium may not function effectively in removal of vasoactive agents and may not release effective quantities of the inhibitor of platelet function or the activator of plasminogen. Altered endothelium exhibits tissue-factor activity, which can activate the extrinsic blood coagulation-system cascade. Finally, altered endothelial cells may contract and expose basement membrane to blood, thus enhancing thrombosis.
对内皮功能重新产生的兴趣部分基于内皮细胞组织培养的成功。内皮主要在控制血管壁通透性以及提供与血液相容的内衬表面方面发挥作用。最近的研究结果表明,内皮细胞在代谢方面很活跃,其方式可能有助于预防血栓形成。内皮能积极降解血液中循环的几种不同的血管活性化合物,这些化合物可作为血小板聚集剂。内皮还含有血小板功能抑制剂和纤溶酶原激活剂,二者均可在适当刺激下从细胞中释放出来。完整的内皮主要在预防血栓形成方面发挥作用,而受损的内皮则可极大地促进血栓形成。受损内皮释放的前列腺素、腺嘌呤核苷酸及其他细胞内成分可增强血小板聚集。受损内皮在清除血管活性物质方面可能无法有效发挥作用,且可能无法释放有效量的血小板功能抑制剂或纤溶酶原激活剂。改变的内皮表现出组织因子活性,可激活外源性血液凝固系统级联反应。最后,改变的内皮细胞可能收缩并使基底膜暴露于血液中,从而增强血栓形成。