Iwasaki K, Kikuchi H, Miyatake S, Aoki T, Yamasaki T, Oda Y
Department of Neurosurgery, Kyoto University Medical School, Japan.
Cancer Res. 1990 Apr 15;50(8):2429-36.
In the present study, we investigated not only the cytotoxic effects of lymphokine-activated killer (LAK) cells on a tumor mass but also the ultrastructural cell-to-cell interaction between LAK effector cells and tumor cells during the cytolytic process within a three-dimensional solid tumor. A multicellular tumor spheroid of a human glioma cell line (U-251MG) was utilized as a solid tumor model. LAK cells were generated from peripheral blood lymphocytes of a healthy donor after stimulation by interleukin 2. Multicellular tumor spheroids with diameters of 500 microns were cocultivated with either LAK cells or nonactivated peripheral blood lymphocytes at the effector:target cell ratio of 20:1, and then time-sequential kinetic, morphological, and ultrastructural analyses were carried out. Morphological and kinetic studies showed that LAK cells directly infiltrated toward the inner areas of multicellular tumor spheroids and caused a progressive tumor destruction. In contrast, peripheral blood lymphocytes hardly exhibited such activities. Ultrastructurally, it was found that the infiltrating LAK effector cells were composed of heterogeneous subpopulations, T-like cells, and large granular lymphocyte-like cells. Both types of lymphocytes tightly adhered to the tumor cells and showed typical morphological features of killing them.
在本研究中,我们不仅研究了淋巴因子激活的杀伤(LAK)细胞对肿瘤块的细胞毒性作用,还研究了在三维实体瘤内的细胞溶解过程中,LAK效应细胞与肿瘤细胞之间的超微结构细胞间相互作用。用人胶质瘤细胞系(U-251MG)的多细胞肿瘤球体作为实体瘤模型。通过白细胞介素2刺激后,从健康供体的外周血淋巴细胞中产生LAK细胞。将直径为500微米的多细胞肿瘤球体与LAK细胞或未激活的外周血淋巴细胞以效应细胞:靶细胞比例为20:1进行共培养,然后进行时间序列动力学、形态学和超微结构分析。形态学和动力学研究表明,LAK细胞直接向多细胞肿瘤球体的内部区域浸润,并导致肿瘤逐渐破坏。相比之下,外周血淋巴细胞几乎没有表现出这种活性。在超微结构上,发现浸润的LAK效应细胞由异质性亚群、T样细胞和大颗粒淋巴细胞样细胞组成。这两种类型的淋巴细胞都紧密粘附于肿瘤细胞,并表现出杀死它们的典型形态学特征。