Basse P H, Nannmark U, Johansson B R, Herberman R B, Goldfarb R H
Department of Pathology, University of Pittsburgh School of Medicine, Pa.
J Natl Cancer Inst. 1991 Jul 3;83(13):944-50. doi: 10.1093/jnci/83.13.944.
A murine model of pulmonary B16 melanoma was used to study the infiltration into metastases of lymphokine-activated killer (LAK) cells and adherent lymphokine-activated killer (A-LAK) cells and, specifically, to study whether A-LAK cells are able to leave the tumor microcirculation and establish cell-to-cell contact with malignant cells. Fluorescence microscopy demonstrated that A-LAK cells accumulated in metastases twice as efficiently as LAK cells during interleukin-2 stimulation. Electron microscopy of pulmonary metastases 16 hours after administration of 2.5 x 10(7) A-LAK cells revealed A-LAK cells, identified by the presence of typical two-compartment granules, in direct contact with melanoma cells. This finding was confirmed by using A-LAK cells prelabeled with polycationized ferritin. In conclusion, our observations demonstrate unambiguously the ability of adoptively transferred A-LAK cells to establish contact with extravascular metastatic melanoma cells.
采用小鼠肺B16黑色素瘤模型来研究淋巴因子激活的杀伤细胞(LAK细胞)和黏附性淋巴因子激活的杀伤细胞(A-LAK细胞)向转移灶的浸润情况,具体而言,是研究A-LAK细胞是否能够离开肿瘤微循环并与恶性细胞建立细胞间接触。荧光显微镜检查显示,在白细胞介素-2刺激期间,A-LAK细胞在转移灶中的聚集效率是LAK细胞的两倍。在给予2.5×10⁷个A-LAK细胞16小时后,对肺转移灶进行电子显微镜检查,发现具有典型双室颗粒的A-LAK细胞与黑色素瘤细胞直接接触。使用聚阳离子化铁蛋白预标记的A-LAK细胞证实了这一发现。总之,我们的观察结果明确表明了过继转移的A-LAK细胞与血管外转移性黑色素瘤细胞建立接触的能力。