Higashi N, Yamauchi M, Okumura Y, Nakanishi M, Sunamoto J
Supermolecules Project, Research Development Corporation of Japan (JRDC), Kyoto, Japan.
Biochim Biophys Acta. 1996 Dec 4;1285(2):183-91. doi: 10.1016/s0005-2736(96)00159-9.
Direct fusion between Jurkat cell and a liposome modified with poly(ethylene oxide)-bearing lipid (PEO-lipid) was examined using diphtheria toxin fragment A (DTA) as the probe. Only the DTA-loaded liposome modified with PEO-lipid(n = 32) (n is the number of ethylene oxide units) exerted significant cytotoxicity against Jurkat cells, while liposomes lacking either the PEO-lipid or DTA did not. Liposomes modified by the PEO-lipid with shorter PEO chain(n = 5 or 15) did not show any cytotoxicity, irrespective of their DTA-loading. The cytotoxicity was observed even in the presence of cytochalasin B, an inhibitor of endocytosis. Judging from these results, we concluded that the PEO-lipid(n = 32)-modified liposome directly fused with plasma membrane of Jurkat cell.
使用白喉毒素片段A(DTA)作为探针,研究了Jurkat细胞与用含聚环氧乙烷脂质(PEO-脂质)修饰的脂质体之间的直接融合。只有用PEO-脂质(n = 32)(n为环氧乙烷单元数)修饰的负载DTA的脂质体对Jurkat细胞具有显著的细胞毒性,而缺乏PEO-脂质或DTA的脂质体则没有。用较短PEO链(n = 5或15)的PEO-脂质修饰的脂质体,无论其是否负载DTA,均未表现出任何细胞毒性。即使在存在内吞作用抑制剂细胞松弛素B的情况下,也观察到了细胞毒性。根据这些结果,我们得出结论,PEO-脂质(n = 32)修饰的脂质体与Jurkat细胞的质膜直接融合。