Rothberger H, McGee M P
J Exp Med. 1984 Dec 1;160(6):1880-90. doi: 10.1084/jem.160.6.1880.
Alveolar macrophages are cell's important in immune defense and inflammation in the lung, and the coagulation system participates in these reactions. In earlier experiments, it was found that alveolar macrophages contain and produce tissue factor, the extrinsic clotting pathway activator. The present experiments explore possible production by alveolar macrophages of the sequence of the clotting proteins that interact to form thrombin following initiation of coagulation by tissue factor. In studies using alveolar macrophages purified from rabbits, factor V activity was not detected in cell preparations assayed directly after isolation. However, after short-term culture, we found generation and release of factor V activity by these cells, which was predominantly from subpopulations with densities of 1.060-1.068 g/ml, corresponding to intermediate stages of alveolar macrophage maturation. Cell viability and protein synthesis were required for generation of the activity as shown by inhibitory effects of cell lysis before culture and by effects observed after including puromycin in cultures with viable cells. The activity generated was characterized as factor V by demonstrating specific functional requirements in one- and two-stage coagulation tests. There was no detectable generation in these cultures of factors II, VII, X, or the more recently described factor X-independent monocyte/macrophage prothrombinases. Factor V activity generated by alveolar macrophages may contribute to prothrominase assembly, activation of clotting, and fibrin formation within the alveolus.
肺泡巨噬细胞是肺部免疫防御和炎症反应中的重要细胞,凝血系统也参与这些反应。在早期实验中,发现肺泡巨噬细胞含有并产生组织因子,即外源性凝血途径激活剂。本实验探讨了肺泡巨噬细胞在组织因子启动凝血后,是否可能产生相互作用形成凝血酶的一系列凝血蛋白。在使用从兔子中纯化的肺泡巨噬细胞进行的研究中,刚分离的细胞制剂中未检测到因子V活性。然而,短期培养后,我们发现这些细胞产生并释放了因子V活性,其主要来自密度为1.060 - 1.068 g/ml的亚群,这与肺泡巨噬细胞成熟的中间阶段相对应。如培养前细胞裂解的抑制作用以及在有活力细胞的培养物中加入嘌呤霉素后观察到的效果所示,产生该活性需要细胞活力和蛋白质合成。通过在一期和二期凝血试验中证明特定的功能需求,将产生的活性鉴定为因子V。在这些培养物中未检测到因子II、VII、X或最近描述的不依赖因子X的单核细胞/巨噬细胞凝血酶原酶的产生。肺泡巨噬细胞产生的因子V活性可能有助于凝血酶原酶组装、凝血激活以及肺泡内纤维蛋白形成。