GFP expression by intracellular gene delivery of GFP-coding fragments using nanocrystal quantum dots

被引:17
作者
Hoshino, Akiyoshi [1 ,2 ]
Manabe, Noriyoshi [1 ,3 ]
Fujioka, Kouki [1 ]
Hanada, Sanshiro [1 ,3 ]
Yasuhara, Masato [2 ]
Kondo, Akihiko [4 ]
Yamamoto, Kenji [1 ,2 ]
机构
[1] Int Med Ctr Japan, Res Inst, Int Clin Res Ctr, Shinjuku Ku, Tokyo 1628655, Japan
[2] Tokyo Med & Dent Univ, Grad Sch, Hosp Pharm, Dept Pharmacokinet & Pharmacodynam,Bunkyo Ku, Tokyo 1138519, Japan
[3] Japan Assoc Adv Med Equipment, Bunkyo Ku, Tokyo 1130033, Japan
[4] Kobe Univ, Grad Sch Engn, Dept Chem Sci & Engn, Nada Ku, Kobe, Hyogo 6578501, Japan
基金
日本学术振兴会;
关键词
D O I
10.1088/0957-4484/19/49/495102
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Gene therapy is an attractive approach to supplement a deficient gene function. Although there has been some success with specific gene delivery using various methods including viral vectors and liposomes, most of these methods have a limited efficiency or also carry a risk for oncogenesis. We herein report that quantum dots (QDs) conjugated with nuclear localizing signal peptides (NLSP) successfully introduced gene-fragments with promoter elements, which promoted the expression of the enhanced green fluorescent protein (eGFP) gene in mammalian cells. The expression of eGFP protein was observed when the QD/gene-construct was added to the culture media. The gene-expression efficiency varied depending on multiple factors around QDs, such as (1) the reading direction of the gene-fragments, (2) the quantity of gene-fragments attached on the surface of the QD-constructs, (3) the surface electronic charges varied according to the structure of the QD/gene-constructs, and (4) the particle size of QD/gene complex varied according to the structure and amounts of gene-fragments. Using this QD/gene-construct system, eGFP protein could be detected 28 days after the gene-introduction whereas the fluorescence of QDs had disappeared. This system therefore provides another method for the intracellular delivery of gene-fragments without using either viral vectors or specific liposomes.
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页数:12
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