Moore K L, Andreoli S P, Esmon N L, Esmon C T, Bang N U
J Clin Invest. 1987 Jan;79(1):124-30. doi: 10.1172/JCI112772.
Endotoxemia is frequently associated clinically with disseminated intravascular coagulation (DIC); however, the mechanism of endotoxin action in vivo is unclear. Modulation of tissue factor (TF) and thrombomodulin (TM) expression on the endothelial surface may be relevant pathophysiologic mechanisms. Stimulation of human umbilical vein endothelial cells with endotoxin (1 microgram/ml) increased surface TF activity from 1.52 +/- 0.84 to 11.89 +/- 8.12 mU/ml-10(6) cells at 6 h (n = 11) which returned to baseline by 24 h. Repeated stimulation at 24 h resulted in renewed TF expression. Endotoxin (1 microgram/ml) also caused a decrease in TM expression to 55.0 +/- 6.4% of control levels at 24 h (n = 10) that remained depressed at 48 h. Both effects were dose and serum dependent. A temporary rise in TF expression accompanied by a sustained fall in TM expression comprise a shift in the hemostatic properties of the endothelium that would favor intravascular coagulation and may contribute to the pathogenesis of DIC in gram-negative septicemia.
内毒素血症在临床上常与弥散性血管内凝血(DIC)相关;然而,内毒素在体内的作用机制尚不清楚。内皮表面组织因子(TF)和血栓调节蛋白(TM)表达的调节可能是相关的病理生理机制。用内毒素(1微克/毫升)刺激人脐静脉内皮细胞,6小时时表面TF活性从1.52±0.84增加到11.89±8.12毫单位/毫升-10(6)细胞(n = 11),24小时时恢复到基线水平。在24小时重复刺激导致TF再次表达。内毒素(1微克/毫升)还使TM表达在24小时时降至对照水平的55.0±6.4%(n = 10),并在48小时时仍保持较低水平。这两种效应均呈剂量和血清依赖性。TF表达的暂时升高伴随着TM表达的持续下降,构成了内皮止血特性的转变,这将有利于血管内凝血,并可能促成革兰氏阴性败血症中DIC的发病机制。