Lifelong reporter gene imaging in the lungs of mice following polyethyleneimine-mediated sleeping-beauty transposon delivery

被引:9
作者
Lin, Erh-Hsuan [1 ,2 ,3 ]
Keramidas, Michelle [4 ,5 ]
Rome, Claire [4 ,5 ]
Chiu, Wen-Ta [6 ]
Wu, Cheng-Wen [3 ]
Coll, Jean-Luc [4 ,5 ]
Deng, Win-Ping [1 ,2 ]
机构
[1] Taipei Med Univ, Inst Biomed Mat & Engn, Taipei, Taiwan
[2] Taipei Med Univ, Ctr Excellence Canc Res, Taipei, Taiwan
[3] Natl Yang Ming Univ, Inst Biochem & Mol Biol, Taipei 112, Taiwan
[4] INSERM, U823, Grenoble, France
[5] Univ Grenoble 1, Grenoble, France
[6] Taipei Med Univ & Hosp, Sch Med, Dept Surg, Taipei, Taiwan
关键词
Non-invasive bioluminescent imaging (BLI); Polyethyleneimine (PEI); Sleeping-Beauty (SB); Alveolar epithelial cells (AECs); LONG-TERM EXPRESSION; IN-VIVO; PHENOTYPIC CORRECTION; SOMATIC INTEGRATION; CELL-PROLIFERATION; HEMOPHILIC MICE; STEM-CELLS; GERM-LINE; SYSTEM; THERAPY;
D O I
10.1016/j.biomaterials.2010.11.026
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polyethyleneimine (PEI) is a cationic polymer that is effective in gene delivery in vivo. Plasmid DNA incorporating the Sleeping-Beauty (SB) transposon has been shown to induce long-term transgene expression in mouse lungs after PEI-mediated delivery. In the current report, we followed the reporter gene expression mediated by PEI/SB delivery in lungs of mice using the non-invasive bioluminescent imaging (BLI) technology. After delivery, the reporter gene signal showed a rapid decay in the first two weeks to a nearly undetectable level, but then the signal augmented gradually in the following weeks and finally reached a stable level that maintained until the natural death of animals. The stabilization of transgene expression is associated with the multiplication of a small number of PEI/SB-labeled alveolar cells, which proliferated both under normal conditions and in response to acute local injury for epithelia repair, and may play a role in long-term homeostatic maintenance in alveoli. The data presented here suggests that systemic delivery of PEI/SB induces stable transfection specifically in a small population of alveolar progenitor cells. The technique provides a promising platform for future research in distal lung biology and tissue regenerative therapy. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1978 / 1985
页数:8
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