Nano R, Barni S, Capelli E, Cremaschi P, Catanese C, Tomaselli S, Nascimbene C, Prosperi E
Department of Animal Biology, University of Pavia, Italy.
Acta Oncol. 1994;33(2):165-9. doi: 10.3109/02841869409098399.
Ultrastructural and fluorescence data allowed us to study the most important moments of the interaction between lymphokine-activated killer (LAK) cells against target cells (Chang) in vitro. The LAK cells, maintained at low doses of recombinant interleukin-2, were able to recognize, bind and destroy the tumoral cells. Before the attack, the LAK cells were characterized by a cytoplasm with a high ribosomes content; after the identification and the interaction cell-cell, a degeneration of the tumoral cell was observed. These observations allowed us to suppose that the interaction between the two types of cells may be mediated by a receptoral membrane system without the action of lytic enzymes.
超微结构和荧光数据使我们能够在体外研究淋巴因子激活的杀伤(LAK)细胞与靶细胞(Chang细胞)相互作用的最重要时刻。维持在低剂量重组白细胞介素-2条件下的LAK细胞能够识别、结合并破坏肿瘤细胞。在攻击之前,LAK细胞的特征是细胞质中核糖体含量高;在识别和细胞间相互作用之后,观察到肿瘤细胞发生退化。这些观察结果使我们推测,两种细胞之间的相互作用可能由受体膜系统介导,而无需溶酶体酶的作用。