Glycofection: facilitated gene transfer by cationic glycopolymers

被引:58
作者
Roche, AC
Fajac, I
Grosse, S
Frison, N
Rondanino, C
Mayer, R
Monsigny, M
机构
[1] CNRS, Ctr Biophys Mol, F-45071 Orleans 02, France
[2] Univ Orleans, F-45071 Orleans, France
[3] Univ Paris 05, CHU Cochin, Physiol Resp Lab, Paris, France
关键词
cystic fibrosis; gene therapy; glycosylated polymers; intracellular traffic; endogenous lectins; nuclear import; polyethyleneimine; polylysine;
D O I
10.1007/s000180300024
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
Mammalian cells express several types of lectins involved in intracellular trafficking, including endocytosis, interorganelle routing and putatively nuclear import. In order to enhance the gene transfer efficiency, glycosylated cationic polymers have been used as nonviral vectors. We developed a simple method to convert reducing saccharides into glycosynthons. Glycosynthons are used to synthesize cationic glycopolymers, called Glycofectins. Glycofectins interact with a plasmid to give a glycoplex, a compacted form of a polymer/DNA complex. The high glycoplex efficiency depends on the sugar involved in the uptake and in the intracellular trafficking of glycoplexes. The present paper deals with glycoplexes, with gene transfer into cystic fibrosis airway epithelial and gland serous cells, and with some of the problems that have to be solved before clinical trials.
引用
收藏
页码:288 / 297
页数:10
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