Coupling of cell-binding ligands to polyethylenimine for targeted gene delivery

被引:315
作者
Kircheis, R
Kichler, A
Wallner, G
Kursa, M
Ogris, M
Felzmann, T
Buchberger, M
Wagner, E
机构
[1] BOEHRINGER INGELHEIM, RES & DEV, VIENNA, AUSTRIA
[2] ST ANNA CHILDRENS HOSP, CHILDRENS CANC RES INST, A-1090 VIENNA, AUSTRIA
[3] UNIV VIENNA, INST BIOCHEM, A-1090 VIENNA, AUSTRIA
基金
奥地利科学基金会;
关键词
gene transfer; polyethylenimine; transferrin receptor; CD3;
D O I
10.1038/sj.gt.3300418
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
Recently the high transfection potential of the cationic polymer polyethylenimine (PEI) was described (Boussif O et al. Proc Natl Acad Sci USA 1995; 92: 7297-7301). To combine the promising DNA delivering activity of PEI with the concept of receptor-mediated gene delivery, cell-binding ligands (transferrin or antiCD3 antibody) were incorporated by covalent linkage to PEI. DNA complexes of PEI or ligand-PEI conjugates were tested for transfection of cultured neuroblastoma Neuro 2A cells, melanoma B16 or H225 cells, erythroid leukemic K562 cells and T cell leukemia Jurkat E6.1 cells. Depending on the cell line, incorporation of the cell-binding ligand resulted in an up to 1000-fold increased transfection efficiency. This activity depends on ligand-receptor interaction and was observed also at low PEI cation.DNA anion ratios where ligand-free PEI lacks efficiency. Depending on the cell-binding ligand, specific targeting (CD3 antibody, Jurkat cells) can be achieved. Gene transfer can be augmented by the addition of an endosome-destabilizing influenza peptide, but is not dependent on the presence of additional endosomolytic agents. Application of transferrin-PEI for the production of murine interleukin-2 in B16 cells resulted in exceptionally high secretion rates of 19 mu g IL-2 protein per 10(6) cells per 24 h.
引用
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页码:409 / 418
页数:10
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