PLASMA FACTOR TRIGGERING ALTERNATIVE COMPLEMENT PATHWAY ACTIVATION BY LIPOSOMES

被引:24
作者
FUNATO, K [1 ]
YAMASHITA, C [1 ]
KAMADA, J [1 ]
TOMINAGA, S [1 ]
KIWADA, H [1 ]
机构
[1] UNIV TOKUSHIMA,FAC PHARMACEUT SCI,TOKUSHIMA 770,JAPAN
关键词
CETYL ALPHA-D-MANNOSIDE; LIPOSOME; DRUG DELIVERY; ALTERNATIVE COMPLEMENT PATHWAY; COMPLEMENT ACTIVATING FACTOR (CAF);
D O I
10.1023/A:1018952718496
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:372 / 376
页数:5
相关论文
共 31 条
[1]  
ALVING CR, 1991, CRIT REV IMMUNOL, V10, P441
[2]  
ALVING CR, 1977, J IMMUNOL, V118, P342
[3]   PREPARATION AND CHARACTERIZATION OF LIPOSOMES CONTAINING MANNOSYLATED PHOSPHOLIPIDS CAPABLE OF TARGETING DRUGS TO MACROPHAGES [J].
BARRATT, G ;
TENU, JP ;
YAPO, A ;
PETIT, JF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 862 (01) :153-164
[4]   INTERACTIONS OF LIPOSOMES WITH SERUM-PROTEINS [J].
BONTE, F ;
JULIANO, RL .
CHEMISTRY AND PHYSICS OF LIPIDS, 1986, 40 (2-4) :359-372
[5]  
CHONN A, 1992, J BIOL CHEM, V267, P18759
[6]   LECTIN-SPECIFIC TARGETING OF BETA-GLUCOCEREBROSIDASE TO DIFFERENT LIVER-CELLS VIA GLYCOSYLATED LIPOSOMES [J].
DAS, PK ;
MURRAY, GJ ;
ZIRZOW, GC ;
BRADY, RO ;
BARRANGER, JA .
BIOCHEMICAL MEDICINE, 1985, 33 (01) :124-131
[7]  
FINE DP, 1972, J IMMUNOL, V109, P807
[8]   CONTRIBUTION OF COMPLEMENT-SYSTEM ON DESTABILIZATION OF LIPOSOMES COMPOSED OF HYDROGENATED EGG PHOSPHATIDYLCHOLINE IN RAT FRESH PLASMA [J].
FUNATO, K ;
YODA, R ;
KIWADA, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1103 (02) :198-204
[9]  
GHOSH P, 1980, BIOCHIM BIOPHYS ACTA, V632, P562, DOI 10.1016/0304-4165(80)90333-5
[10]  
HARASHIMA H, 1993, PHARMACEUT RES, V11, P402