Polyethyleneimine-mediated gene delivery into human adipose derived stem cells

被引:82
作者
Ahn, Hyun Hee [1 ,2 ]
Lee, Jung Hwa [1 ]
Kim, Kyung Sook [1 ]
Lee, Ju Young [1 ]
Kim, Moon Suk [1 ]
Khang, Gilson [3 ]
Lee, Il Woo [2 ]
Lee, Hai Bang [1 ]
机构
[1] Korea Res Inst Chem Technol, Fus Biotechnol Res Ctr, Taejon 305600, South Korea
[2] Catholic Univ Korea, Dept Neurosurg, Taejon 301723, South Korea
[3] Chonbuk Natl Univ, Polymer BIN Fus Res Team BK 21, Jeonju 561756, South Korea
关键词
human adipose tissue-derived stem cells; gene carrier; polyethylenimine; transfection;
D O I
10.1016/j.biomaterials.2008.02.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study, we examined the use of polyethyleneimine (PEI) as a carrier for gene delivery in human adipose tissue-derived stem cells (hADSCs). These multipotent cells can form bone, cartilage, adipose, and other connective tissues. In primary culture, hADSCs are fibroblastic in appearance in primary culture, and they show a high rate of proliferation for at least five passages. Immunophenotyping showed that these cells are positive for the mesenchymal stem cell markers CD29 and CD44 but negative for the hematopoietic cell surface markers CD34, CD45, and c-kit. PEI and Lipofectamine were compared as gene carriers for hADSCs. DNA completely bound PEI at a negative-to-positive (N/P) charge ratio of 4. The PEI-DNA complexes were spherical with smooth surfaces. As the proportion of PEI was increased, the size of the PEI-DNA complexes decreased from 990 to 130 nm, the positive surface charge decreased, and the cytotoxicity increased. Flow cytometry revealed that the transfection efficiency using PEI at N/P charge ratios of 4 and 8 was higher than that of Lipofectamine. The highest transfection efficiency (19%) was obtained at an N/P charge ratio of 8. After transfection, the enhanced green fluorescent protein (EGFP) started to localize in the nuclei of hADSCs at 4 It 30 m and localize over cytoplasm from 9 It 30 m. In conclusion, PEI acts as an effective gene carrier for hADSCs. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2415 / 2422
页数:8
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