Yamazaki M, Shinoda H, Hattori R, Mizuno D
Gan. 1977 Aug;68(4):513-6.
Cell-free ascites from syngeneic MM46 tumor-bearing C3H/He mice inhibited the antibody-dependent macrophage-mediated tumor lysis in vitro and the inhibitiory activity increased with the period of tumor bearing. Thus, the inhibitory activity was demonstrated at the effector cell level. Three fractions of lipoprotein and a protein-rich fraction were prepared from the cell-free ascites by sequential flotation. Among these, the very low density (p less than 1.006) and low density (1.006 less than p less than 1.063) lipoprotein fractions inhibited tumor lysis mediated by activated macrophages and syngeneic antitumor antibody, whereas the high density (1.063 less than p less than 1.21) lipoprotein and the protein-rich infranatant fractions did not. This inhibitory activity at the effector cell level may be due to functional depression of macrophages by lipoprotein fractions.
来自同基因携带MM46肿瘤的C3H/He小鼠的无细胞腹水在体外抑制了抗体依赖性巨噬细胞介导的肿瘤溶解,并且抑制活性随着荷瘤时间的延长而增加。因此,这种抑制活性在效应细胞水平得到了证实。通过连续浮选从无细胞腹水中制备了三部分脂蛋白和一个富含蛋白质的部分。其中,极低密度(p小于1.006)和低密度(1.006小于p小于1.063)脂蛋白部分抑制了由活化巨噬细胞和同基因抗肿瘤抗体介导的肿瘤溶解,而高密度(1.063小于p小于1.21)脂蛋白和富含蛋白质的下层部分则没有。效应细胞水平的这种抑制活性可能是由于脂蛋白部分对巨噬细胞的功能抑制。