Zuckerman S H, Suprenant Y M
Department of Immunology, Lilly Research Labs, Indianapolis, IN 46285.
Thromb Haemost. 1989 Apr 25;61(2):178-82.
Inflammatory mediators such as endotoxin can stimulate the expression of procoagulant activity on both endothelial cells and macrophages while the monokines Interleukin 1, IL-1, and Tumor Necrosis Factor, TNF, induce procoagulant activity on endothelial cells. Incubation of murine peritoneal macrophages with suboptimal concentrations of endotoxin results in a two fold increase in procoagulant activity. Macrophages incubated with gamma interferon, IFN gamma, or Granulocyte-Macrophage Colony Stimulating Factor, GM-CSF, for 16 hours prior to endotoxin stimulation demonstrated a synergistic increase in procoagulant activity. A synergistic increase in procoagulant activity was also observed with primary cultures of human umbilical cord endothelial cells incubated with recombinant human IFN gamma for 16 hours prior to endotoxin, TNF, or IL-1 stimulation. Human GM-CSF had no stimulatory effect on endotoxin or monokine induced endothelial cell procoagulant activity. The augmentation of macrophage and endothelial cell procoagulant activity by IFN gamma and GM-CSF may provide a novel explanation for the role of these cytokines in acute and chronic inflammation.
内毒素等炎症介质可刺激内皮细胞和巨噬细胞上促凝活性的表达,而单核因子白细胞介素1(IL-1)和肿瘤坏死因子(TNF)可诱导内皮细胞产生促凝活性。用次优浓度的内毒素孵育小鼠腹膜巨噬细胞会导致促凝活性增加两倍。在内毒素刺激前16小时,用γ干扰素(IFNγ)或粒细胞-巨噬细胞集落刺激因子(GM-CSF)孵育巨噬细胞,促凝活性呈协同增加。在内毒素、TNF或IL-1刺激前16小时,用重组人IFNγ孵育人脐带内皮细胞原代培养物,也观察到促凝活性的协同增加。人GM-CSF对内皮细胞促凝活性没有刺激作用。IFNγ和GM-CSF增强巨噬细胞和内皮细胞的促凝活性,可能为这些细胞因子在急慢性炎症中的作用提供新的解释。