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人血单核细胞、胸腔积液和腹水中巨噬细胞以及肺泡巨噬细胞的增殖活性和抑菌潜力。

Proliferation activity and bacteriostatic potential of human blood monocytes, macrophages in pleural effusions, ascites, and of alveolar macrophages.

作者信息

Meuret G, Schildknecht O, Joder P, Senn H

出版信息

Blut. 1980 Jan;40(1):17-25. doi: 10.1007/BF01028360.

Abstract

Human blood monocytes, macrophages from pleural effusions, ascites, and alveolar macrophages obtained by bronchopulmonary lavage were investigated. The proliferative activity of these cells was determined by the 3H-thymidine labeling index in vitro (3H-TDR L.I.). The bacteriostatic capacity was measured by the potential of the cells to block DNA-synthesis of proliferating Escherichia coli after phagocytosis. In most cases 3H-TDR L.I. of blood monocytes, macrophages from pleural effusions and ascites was less than 1%. However, macrophages of some patients with neoplastic diseases exhibited 3H-TDR L.I. between 4.0--9.6%. This probably reflected the action of factors, possibly lymphokines, which stimulated macrophage proliferation. In contrast, alveolar macrophages seemed to have almost totally lost their proliferative potential. The bacteriostatic capacity of blood monocytes proved to be significantly lower than that of macrophages. This demonstrates the functional immaturity of blood monocytes. In all type of macrophages investigated the bacteriostatic power was very high. No differences could be detected either between macrophages of different sources or between macrophages of benign, inflammatory, or malignant diseases.

摘要

对人血单核细胞、来自胸腔积液、腹水的巨噬细胞以及通过支气管肺灌洗获得的肺泡巨噬细胞进行了研究。这些细胞的增殖活性通过体外3H-胸腺嘧啶核苷标记指数(3H-TDR L.I.)来测定。抑菌能力通过吞噬后细胞阻断增殖性大肠杆菌DNA合成的能力来衡量。在大多数情况下,血单核细胞、胸腔积液和腹水来源的巨噬细胞的3H-TDR L.I.小于1%。然而,一些肿瘤疾病患者的巨噬细胞表现出3H-TDR L.I.在4.0%至9.6%之间。这可能反映了可能是淋巴因子等因子刺激巨噬细胞增殖的作用。相比之下,肺泡巨噬细胞似乎几乎完全丧失了增殖潜能。血单核细胞的抑菌能力被证明明显低于巨噬细胞。这表明血单核细胞功能不成熟。在所研究的所有类型巨噬细胞中,抑菌能力都非常高。在不同来源的巨噬细胞之间或良性、炎症性或恶性疾病的巨噬细胞之间均未检测到差异。

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