Swinburne S, Moore M, Cole P
Br J Cancer. 1982 Oct;46(4):625-34. doi: 10.1038/bjc.1982.247.
Human bronchoalveolar macrophages were separated from other free lung cells by density sedimentation on Percoll gradients. They were then tested for cytotoxicity against the human lung adenocarcinoma cell line A549, using a Selenomethionine-75 post-labelling assay. The cytotoxicity of the macrophages increased as the effector:target cell ratio was increased, approaching 100% at 20:1. There was no significant difference in the cytotoxicity of macrophages isolated from the lungs of bronchial-carcinoma or non-carcinoma patients. The highly cytotoxic nature of the macrophages was not due to selection of a more potent cytotoxic subpopulation of macrophages on the Percoll gradient, nor to a generally elevated activation of the macrophages due to the pathological conditions in the patients' lungs. An attempt to determine whether low concentrations of macrophages could potentiate target-cell growth proved negative. Cytotoxicity of macrophages for cultured lung target cells was not restricted to A549 cells and is not in accordance with the view that defective bronchoalveolar macrophage cytotoxicity contributes to the emergence of bronchial neoplasia.
通过在Percoll梯度上进行密度沉降,将人支气管肺泡巨噬细胞与其他游离肺细胞分离。然后,使用硒代蛋氨酸-75后标记试验,检测它们对人肺腺癌细胞系A549的细胞毒性。随着效应细胞与靶细胞比例的增加,巨噬细胞的细胞毒性增强,在20:1时接近100%。从支气管癌或非癌患者肺部分离的巨噬细胞的细胞毒性没有显著差异。巨噬细胞的高细胞毒性并非由于在Percoll梯度上选择了更具细胞毒性的巨噬细胞亚群,也不是由于患者肺部的病理状况导致巨噬细胞普遍活化增强。试图确定低浓度的巨噬细胞是否能促进靶细胞生长的实验结果为阴性。巨噬细胞对培养的肺靶细胞的细胞毒性并不局限于A549细胞,这与支气管肺泡巨噬细胞细胞毒性缺陷导致支气管肿瘤发生的观点不一致。