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Human bronchoalveolar macrophage cytotoxicity for cultured human lung-tumour cells.

机译:人支气管肺泡巨噬细胞对培养的人肺肿瘤细胞的细胞毒性。

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摘要

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.
机译:通过Percoll梯度上的密度沉淀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Selenomethionine-75标记后测定法测试它们对人肺腺癌细胞A549的细胞毒性。巨噬细胞的细胞毒性随着效应子:靶细胞比例的增加而增加,在20:1时接近100%。从支气管癌或非癌患者的肺中分离出的巨噬细胞的细胞毒性没有显着差异。巨噬细胞的高度细胞毒性性质不是由于在Percoll梯度上选择了更有效的巨噬细胞毒性亚群,也不是由于患者肺部的病理状况导致巨噬细胞的活化普遍升高。试图确定低浓度的巨噬细胞是否可以增强靶细胞的生长被证明是负面的。巨噬细胞对培养的肺靶细胞的细胞毒性不限于A549细胞,也不符合认为支气管肺泡巨噬细胞缺陷性细胞毒性导致支气管肿瘤形成的观点。

著录项

  • 作者单位
  • 年度 1982
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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