Hara T, Kuwasawa H, Aramaki Y, Takada S, Koike K, Ishidate K, Kato H, Tsuchiya S
Department of Biopharmaceutics, School of Pharmacy, Tokyo University of Pharmacy and Life Science, Japan.
Biochim Biophys Acta. 1996 Jan 12;1278(1):51-8. doi: 10.1016/0005-2736(95)00205-7.
Effects of fusogenic and DNA-binding amphiphilic compounds on the receptor-mediated gene transfer using asialofetuin-labeled liposomes (AF-liposomes) were examined with HepG2 cells and rat hepatocytes in primary culture. AF-liposomes were sufficiently taken up by both types of cells through the asialoglycoprotein receptor-mediated endocytosis. In HepG2 cells, bacterial beta-galactosidase (beta-Gal) gene expression was observed by transfection using AF-liposomes encapsulating plasmid pCMV beta DNA (AF-liposome-pCMV beta). By addition of dioleoylphosphatidylethanolamine (DOPE) to the liposomal lipid composition (AF-liposome(DOPE)-pCMV beta), the transfection efficiency was clearly increased. The effects of DOPE were more conspicuous in the presence of chloroquine in the medium throughout the transfection. When pCMV beta complexed with gramicidin S (pCMV beta (GrS)) was encapsulated (AF-liposome(DOPE)-pCMV beta (GrS) and was transfected to HepG2 cells, an significantly high beta-Gal activity in the cells was observed as compared with that in the cells transfected with AF-liposome(DOPE)-pCMV beta. No effects of GrS were found in the transfection using AF-non-labeled control liposomes. In primary culture of rat hepatocytes, no beta-Gal gene expression was observed even though AF-liposome(DOPE)-pCMV beta was introduced into the cells prepared from adult rats. However, following the transfection with AF-liposome(DOPE)-pCMV beta, the beta-Gal activity was expressed in the cells from immature rats cultured in the medium supplemented with epidermal growth factor and insulin, and the transfection efficiency was 2-fold higher than that transfected with pCMV beta encapsulated in AF-non-labeled control liposomes. By the complex formation of pCMV beta with GrS, the transfection efficiency of AF-liposome(DOPE)-pCMV beta (GrS) increased according to the increase of GrS in the complex. It was shown that AF-liposome(DOPE)-pCMV beta (GrS) did efficiently introduce and express beta-Gal gene in both HepG2 cells and primary hepatocytes in the receptor mediated manner.
利用去唾液酸胎球蛋白标记的脂质体(AF-脂质体),在HepG2细胞和原代培养的大鼠肝细胞中研究了融合性和DNA结合两亲化合物对受体介导基因转移的影响。两种细胞均可通过去唾液酸糖蛋白受体介导的内吞作用充分摄取AF-脂质体。在HepG2细胞中,通过使用包裹质粒pCMV β DNA的AF-脂质体(AF-脂质体-pCMV β)进行转染,观察到细菌β-半乳糖苷酶(β-Gal)基因表达。通过向脂质体脂质组成中添加二油酰磷脂酰乙醇胺(DOPE)(AF-脂质体(DOPE)-pCMV β),转染效率明显提高。在整个转染过程中,培养基中存在氯喹时,DOPE的作用更为显著。当与短杆菌肽S复合的pCMV β(pCMV β(GrS))被包裹(AF-脂质体(DOPE)-pCMV β(GrS))并转染到HepG2细胞中时,与用AF-脂质体(DOPE)-pCMV β转染的细胞相比,观察到细胞中β-Gal活性显著升高。在使用AF-未标记对照脂质体进行的转染中未发现GrS的作用。在大鼠肝细胞原代培养中,即使将AF-脂质体(DOPE)-pCMV β引入成年大鼠制备的细胞中,也未观察到β-Gal基因表达。然而,在用AF-脂质体(DOPE)-pCMV β转染后,在补充有表皮生长因子和胰岛素的培养基中培养的未成熟大鼠的细胞中表达了β-Gal活性,且转染效率比用包裹在AF-未标记对照脂质体中的pCMV β转染的效率高2倍。通过pCMV β与GrS的复合形成,AF-脂质体(DOPE)-pCMV β(GrS)的转染效率随着复合物中GrS的增加而提高。结果表明,AF-脂质体(DOPE)-pCMV β(GrS)确实以受体介导的方式在HepG2细胞和原代肝细胞中有效导入并表达β-Gal基因。