Takemura-Hattori R, Yamazaki M, Kurisu M, Mizuno D
Gan. 1980 Apr;71(2):206-12.
Various tumorous ascites inhibited the antibody-dependent macrophage-mediated tumor lysis in vitro (ADMC) which had been found in a C3H/He mouse-MM46 tumor system. This inhibition of ADMC was due to functional depression of effector macrophages, evidenced by in vitro and in vivo pretreatment of effector cells with ascites lipoprotein. Ascites lipoprotein also had direct cytotoxicity against various cells, but in the ADMC system, two activities appeared separately; lower concentrations of lipoprotein caused inhibition of ADMC and higher one caused cytotoxicity to macrophages and tumor cells. The component of lipoprotein active in these two activities was the lipid moiety. These results suggest that lipoprotein in tumorous ascities depresses the function of macrophages resulting in the inhibition of ADMC and that lipid moiety is the essential component.
在C3H/He小鼠-MM46肿瘤系统中发现,各种肿瘤腹水在体外抑制了抗体依赖性巨噬细胞介导的肿瘤溶解作用(ADMC)。ADMC的这种抑制是由于效应巨噬细胞的功能抑制,用腹水脂蛋白对效应细胞进行体外和体内预处理可证明这一点。腹水脂蛋白对各种细胞也有直接细胞毒性,但在ADMC系统中,这两种活性是分别出现的;较低浓度的脂蛋白导致ADMC受抑制,而较高浓度的脂蛋白则对巨噬细胞和肿瘤细胞产生细胞毒性。在这两种活性中起作用的脂蛋白成分是脂质部分。这些结果表明,肿瘤腹水中的脂蛋白会抑制巨噬细胞的功能,从而导致ADMC受抑制,并且脂质部分是必需成分。