Bloom E T, Babbitt J T
Cell Immunol. 1985 Mar;91(1):21-32. doi: 10.1016/0008-8749(85)90028-0.
Normal human monocytes can significantly and rapidly augment natural cell-mediated cytotoxicity (NCMC) against K562 target cells. Approximately 50% augmentation was observed after direct mixture of monocytes with autologous null cells in the 4-hr chromium-release assay. This effect was dependent on the number of monocytes, and B cells and granulocytes were not effective. Coculture of null cells with monocytes and subsequent recovery of null cells for use as effector cells also produced significantly elevated cytolytic activity. This effect was dependent upon the number of monocytes, the length of time of coculture, and the cell donor. Augmentation of NK activity was rapid and observed after 0.5-12 hr of coculture, but suppression was observed after 36 hr; augmentation was observed with high monocyte:null cell (1:1, 1:2) ratios, and no effect was generally observed with lower ratios (1:8). At the single-cell level, the augmentation was associated with an increase in the proportion of target-binding cells which were lytically active. The augmentation of NK activity by monocytes required close cellular proximity, was mediated by a factor which was active or induced only in close proximity of the effector and producer cells, and/or was mediated by a soluble factor with a molecular weight greater than 50,000. This new demonstration that monocytes can augment as well as suppress NCMC may represent another avenue by which NK cell activity may be modulated in vivo.
正常人单核细胞能够显著且迅速地增强针对K562靶细胞的自然细胞介导的细胞毒性(NCMC)。在4小时的铬释放试验中,将单核细胞与自体无活性细胞直接混合后,观察到约50%的增强效果。这种效应取决于单核细胞的数量,而B细胞和粒细胞则无效。将无活性细胞与单核细胞共培养,随后回收无活性细胞用作效应细胞,也能显著提高细胞溶解活性。这种效应取决于单核细胞的数量、共培养的时间长度以及细胞供体。NK活性的增强迅速,在共培养0.5 - 12小时后即可观察到,但在36小时后观察到抑制现象;在单核细胞与无活性细胞比例较高(1:1、1:2)时观察到增强,而在较低比例(1:8)时通常未观察到效果。在单细胞水平上,这种增强与具有溶解活性的靶结合细胞比例增加有关。单核细胞对NK活性的增强需要细胞紧密接触,由仅在效应细胞和产生细胞紧密接触时才具有活性或被诱导的因子介导,和/或由分子量大于50,000的可溶性因子介导。单核细胞既能增强也能抑制NCMC这一新发现可能代表了体内调节NK细胞活性的另一条途径。