Piessens W F
J Immunol. 1977 Jul;119(1):167-72.
The binding of Line 10 hepatoma cells to normal syngeneic guinea pig macrophages is increased when the tumor cells are treated with neuraminidase and galactose oxidase (NAGO) before they are added to the macrophage monolayers. The effect is abolished by exposure of the NAGO-treated tumor cells to sodium borohydride. Line 1 hepatoma cells treated with NAGO or with sodium periodate are killed to a greater extent than untreated tumor cells. This effect can also be reversed by sodium borohydride. Further, periodate-treated macrophages become cytotoxic for unmodified tumor cells. These results demonstrate that increased tumor cell killing occurs when artificial contacts (presumably via Schiff bases) are established between normal macrophages and tumor cells. They are consistent with the hypothesis that close cell to cell contact is necessary for macrophage-mediated cytotoxicity.
当10号线肝癌细胞在用神经氨酸酶和半乳糖氧化酶(NAGO)处理后再添加到巨噬细胞单层之前,其与同基因正常豚鼠巨噬细胞的结合会增加。将经NAGO处理的肿瘤细胞暴露于硼氢化钠后,这种效应就会消失。用NAGO或高碘酸钠处理的1号线肝癌细胞比未处理的肿瘤细胞死亡程度更大。这种效应也可以被硼氢化钠逆转。此外,经高碘酸钠处理的巨噬细胞对未修饰的肿瘤细胞具有细胞毒性。这些结果表明,当在正常巨噬细胞和肿瘤细胞之间建立人工接触(可能通过席夫碱)时,肿瘤细胞杀伤作用会增强。它们与巨噬细胞介导的细胞毒性需要细胞间紧密接触这一假设相一致。