Nose M, Kamao T, Kyogoku M
Int Arch Allergy Appl Immunol. 1981;65(1):15-22. doi: 10.1159/000232732.
A murine-cultured lymphocytic leukemic cell line, SC-1, showed remarkable cytotoxicity against 51Cr-labeled rabbit erythrocytes as target cells in the presence of antitarget antibodies in vitro. This cytotoxicity was complement independent, inhibited by the addition of aggregated human gamma-globulin, and reduced by pepsin digestion of antitarget IgG. Moreover, SC-1 cells also induced cytotoxicity to trinitrophenyl-modified rabbit erythrocytes in the presence of antitrinitrophenyl antibodies but not unmodified rabbit erythrocytes used as bystander cells. SC-1 cells which showed such K cell activity, however escaped from Fc receptor detection by erythrocyte antibody rosettes and FITC-conjugated aggregated human gamma-globulin binding. In morphological studies using the scanning electron microscope, SC-1 cells to induce cytotoxicity through a light attachment to target cells via 'point contact' of the microvilli. From these findings the characteristics of Fc receptors on effector cells in the mechanism of antibody-dependent cellular cytotoxicity was discussed.
一种在小鼠中培养的淋巴细胞白血病细胞系SC-1,在体外存在抗靶抗体的情况下,对作为靶细胞的51Cr标记的兔红细胞表现出显著的细胞毒性。这种细胞毒性不依赖补体,可被添加的聚合人γ球蛋白抑制,并且通过抗靶IgG的胃蛋白酶消化而降低。此外,在存在抗三硝基苯基抗体的情况下,SC-1细胞也会对三硝基苯基修饰的兔红细胞诱导细胞毒性,但对用作旁观者细胞的未修饰兔红细胞则不会。然而,表现出这种K细胞活性的SC-1细胞,通过红细胞抗体玫瑰花结和异硫氰酸荧光素偶联的聚合人γ球蛋白结合,无法被Fc受体检测到。在使用扫描电子显微镜的形态学研究中,SC-1细胞通过微绒毛的“点接触”与靶细胞轻度附着来诱导细胞毒性。基于这些发现,讨论了抗体依赖性细胞毒性机制中效应细胞上Fc受体的特性。