Collins D, Huang L
Cancer Res. 1987 Feb 1;47(3):735-9.
pH-sensitive immunoliposomes composed of dioleoylphosphatidylethanolamine and oleic acid (8:2 molar ratio) mediated the delivery of the cytotoxic fragment A of diphtheria toxin to the cytoplasm of target L-929 cells. Free fragment A, fragment A encapsulated in antibody-free liposomes, or fragment A encapsulated in pH-insensitive immunoliposomes was not effective in the inhibition of the cellular protein synthesis. pH-sensitive immunoliposomes containing diphtheria fragment A were not toxic to nontarget diphtheria-resistant A31 cells or to nontarget diphtheria-sensitive Vero cells. Pretreatment of target L-929 cells with the weak bases NH4Cl or chloroquine, agents which raise the endosome/lysosome pH, blocked the cytotoxic effect of the pH-sensitive immunoliposomes containing fragment A. Excess free antibody or excess empty pH-sensitive immunoliposomes also blocked the cytotoxic effect. Since it is known that fragment A alone cannot cross lipid membranes, the results of this study indicate that pH-sensitive immunoliposomes are able to release the toxin into the cytoplasm, probably by fusing with the endosome membrane following a receptor-mediated endocytosis of the immunoliposome.
由二油酰磷脂酰乙醇胺和油酸(摩尔比为8:2)组成的pH敏感免疫脂质体将白喉毒素的细胞毒性片段A递送至靶L-929细胞的细胞质中。游离的片段A、包裹在无抗体脂质体中的片段A或包裹在pH不敏感免疫脂质体中的片段A在抑制细胞蛋白质合成方面均无效。含有白喉片段A的pH敏感免疫脂质体对非靶标抗白喉A31细胞或非靶标对白喉敏感的Vero细胞无毒。用弱碱氯化铵或氯喹预处理靶L-929细胞(这些试剂可提高内体/溶酶体pH值)可阻断含有片段A的pH敏感免疫脂质体的细胞毒性作用。过量的游离抗体或过量的空pH敏感免疫脂质体也可阻断细胞毒性作用。由于已知片段A单独不能穿过脂质膜,因此本研究结果表明,pH敏感免疫脂质体可能通过在免疫脂质体受体介导的内吞作用后与内体膜融合,从而将毒素释放到细胞质中。