Delivery and pathway in MCF7 cells of DNA vectorized by cationic liposomes derived from cholesterol

被引:32
作者
Cao, A
Briane, D
Coudert, R
Vassy, J
Lievre, N
Olsman, E
Tamboise, E
Salzmann, JL
Rigaut, JP
Taillandier, E
机构
[1] Univ Paris 13, UFR Med, Lab Chim Struct & Spect Biomol, CNRS,URA 1430, F-93012 Bobigny, France
[2] Fac Sci, EA 2098, Lab Physicochim Interfaces & Milieux React, F-37200 Tours, France
[3] Univ Paris 07, Hop St Louis, Inst Hematol, Lab Anal Images Pathol Cellulaire, F-75010 Paris, France
[4] Univ Paris 13, UFR Med, Lab Histol & Therapie Gen, F-93012 Bobigny, France
来源
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT | 2000年 / 10卷 / 05期
关键词
D O I
10.1089/oli.1.2000.10.369
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have investigated the delivery and the pathway in tumoral MCF7 cells of DNA carried by liposomes prepared from (trimethyl aminoethane carbamoyl cholesterol iodide (TMAE-Chol), a cholesterol-based cationic lipid with a quaternary ammonium on the polar head. The structure of DNA-liposome complexes depends on the length of DNA and on the lipid-DNA charge ratio X. Spherical beads constitute fine structures of the observed complexes even when they appear as aggregates. For oligonucleotide transfer, dissociation from liposomes after transfection, penetration of the oligonucleotides into nuclei, and a long resident time were observed. For plasmid transfer, a correlation between the variation in the transfection level and the ultrastructure of complexes was demonstrated, The results showed a cellular route of lipid/plasmid complexes from the beginning by endocytosis, entrapped into endosomes, released by the latter until entry in the perinuclear area, and then penetration of plasmids inside the nuclei resulting in the observed expression of the beta -galactosidase gene.
引用
收藏
页码:369 / 380
页数:12
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