Niemetz J, Marcus A J
J Clin Invest. 1974 Dec;54(6):1437-43. doi: 10.1172/JCI107891.
Leukocytes can generate procoagulant (tissue factor) activity when incubated with endotoxin. These studies were undertaken to determine whether platelets could influence the procoagulant activity generated by leukocytes. Intact or disrupted platelets (rabbit or human) enhanced the clot-promoting properties of rabbit leukocytes. The enhancing effect of human platelets on human leukocytes required the presence of human serum (devoid of factor VII and X activities). When platelets were incubated with endotoxin in the absence of leukocytes, no increase in their clot-promoting properties was discernible. However, a mixture of platelets, leukocytes, and endotoxin generated procoagulant activity which appeared rapidly and was fivefold greater than that produced by leukocytes incubated with endotoxin alone. The enhancement produced by platelets was even more pronounced if homogenates were used. The platelet effect was examined in more detail by the substitution of membranes, granules, and the "soluble" fraction for whole platelets in the test system. The stimulating activity was localized to the particulate fractions, i.e., membranes and granules. Prior treatment of platelet membranes with phospholipase C or gangliosides or by extraction of lipid resulted in loss of enhancing activity, whereas no inhibition was observed after exposure to neuraminidase or trypsin. It is proposed that platelets contribute a membrane lipoprotein surface which enhances the procoagulant activity generated by leukocytes in the presence of endotoxin. This mechanism may be involved in some of the clinical and pathologic manifestations of gram-negative sepsis with disseminated intravascular coagulation.
白细胞与内毒素一起孵育时可产生促凝血(组织因子)活性。进行这些研究以确定血小板是否会影响白细胞产生的促凝血活性。完整的或破碎的血小板(兔或人)增强了兔白细胞的促凝特性。人血小板对人白细胞的增强作用需要人血清(缺乏因子VII和X活性)的存在。当血小板在无白细胞的情况下与内毒素一起孵育时,其促凝特性没有明显增加。然而,血小板、白细胞和内毒素的混合物产生了促凝血活性,该活性出现迅速,比单独用内毒素孵育的白细胞产生的促凝血活性高五倍。如果使用匀浆,血小板产生的增强作用会更明显。通过在测试系统中用膜、颗粒和“可溶性”部分替代全血小板来更详细地研究血小板的作用。刺激活性定位于颗粒部分,即膜和颗粒。用磷脂酶C或神经节苷脂预处理血小板膜或提取脂质会导致增强活性丧失,而在暴露于神经氨酸酶或胰蛋白酶后未观察到抑制作用。有人提出,血小板提供了一种膜脂蛋白表面,在内毒素存在的情况下增强白细胞产生的促凝血活性。这种机制可能参与了革兰氏阴性菌败血症伴弥散性血管内凝血的一些临床和病理表现。