Kiyohara T, Tanino T, Egawa K
Jpn J Exp Med. 1982 Aug;52(4):201-8.
Normal mouse spleen cells exhibited nonspecific cytotoxicity against MM2 and other NK-insensitive mouse ascites tumor cells after culture for 3 or 4 days in vitro in the presence of heat-inactivated foetal calf serum and 5 X 10(-5) M 2-mercapthoethanol. The cytotoxicity was assayed by 51Cr-release during 18 hr incubation. Culture of spleen cells from C3H/He or C57BL/6 mice resulted in strong cytotoxicity, while cytotoxicity did not appear or appeared only weakly during culture of spleen cells from Balb/c, DDD, DBA/2 or athymic mice. High activity was observed when spleen cells from aged mice were used. The effector cells which lysed MM2 cells seemed glass dish non-adherent, Sephadex G-10 adherent, nylon wool adherent, and Thy 1.2 positive cells. The induction of cytotoxicity was inhibited by adding cytosine arabinoside to the culture medium. Mouse serum was also inhibitory. Restriction specificity between the effector and the targets was not observed for the lytic reaction. By cold target competition experiments, it was shown that the effector cells recognize cell surface structures commonly present on the surface of wide range of tumor cells which are unrelated with respect to tumor specific antigenicity.
正常小鼠脾细胞在含有热灭活胎牛血清和5×10⁻⁵ M 2-巯基乙醇的条件下于体外培养3或4天后,对MM2及其他NK不敏感的小鼠腹水肿瘤细胞表现出非特异性细胞毒性。细胞毒性通过在18小时孵育期间的⁵¹Cr释放来测定。来自C3H/He或C57BL/6小鼠的脾细胞培养产生强烈的细胞毒性,而来自Balb/c、DDD、DBA/2或无胸腺小鼠的脾细胞培养期间细胞毒性未出现或仅微弱出现。使用老龄小鼠的脾细胞时观察到高活性。裂解MM2细胞的效应细胞似乎是非贴壁于玻璃培养皿、可贴壁于Sephadex G-10、可贴壁于尼龙棉且Thy 1.2阳性的细胞。向培养基中添加阿糖胞苷可抑制细胞毒性的诱导。小鼠血清也具有抑制作用。对于裂解反应,未观察到效应细胞与靶细胞之间的限制特异性。通过冷靶竞争实验表明,效应细胞识别广泛的肿瘤细胞表面共同存在的细胞表面结构,这些肿瘤细胞在肿瘤特异性抗原性方面无关。