Funato K, Yamashita C, Kamada J, Tominaga S, Kiwada H
Faculty of Pharmaceutical Sciences, University of Tokushima, Japan.
Pharm Res. 1994 Mar;11(3):372-6. doi: 10.1023/a:1018952718496.
Several plasma components, such as complement (C) components, play a role in the clearance of liposomes from the circulation. The interactions between liposomes and the C system were investigated in this study. Multilamellar vesicle (MLV) liposomes, which were damaged by activation of the complement, became susceptible depending on the density of cetylmannoside (Man) on the liposome membrane, and activation proceeded through the alternative C pathway as observed for liposomes without Man (PC-MLV) (K. Funato et al., Biochim. Biophys. Acta 1103:198-204, 1992). In addition, the capacity of Man-modified liposomes (Man-MLV) to activate the alternative C pathway was abolished by preadsorption of plasma with Man-MLV but not with PC-MLV. The results suggest that a specific plasma factor adsorbed with Man-MLV was responsible for the augmentation of the C activation and, further, that the rapid clearance of Man-MLV from the circulation is caused by both enhanced C-mediated liposome permeability and enhanced C-mediated phagocytosis of liposomes.
几种血浆成分,如补体(C)成分,在脂质体从循环中清除的过程中发挥作用。本研究对脂质体与补体系统之间的相互作用进行了研究。多层囊泡(MLV)脂质体在补体激活后会受到损伤,其敏感性取决于脂质体膜上十六烷基甘露糖苷(Man)的密度,并且激活过程通过替代补体途径进行,这与不含Man的脂质体(PC-MLV)的情况相同(K. Funato等人,《生物化学与生物物理学报》1103:198 - 204,1992)。此外,用Man-MLV预吸附血浆可消除Man修饰的脂质体(Man-MLV)激活替代补体途径的能力,但用PC-MLV预吸附血浆则不能。结果表明,吸附在Man-MLV上的一种特定血浆因子是补体激活增强的原因,而且,Man-MLV从循环中快速清除是由补体介导的脂质体通透性增强和补体介导的脂质体吞噬作用增强共同导致的。