Generation of Induced Pluripotent Stem Cells from Human Nasal Epithelial Cells Using a Sendai Virus Vector

被引:34
|
作者
Ono, Mizuho [1 ]
Hamada, Yuko [1 ]
Horiuchi, Yasue [2 ]
Matsuo-Takasaki, Mami [3 ]
Imoto, Yoshimasa [4 ]
Satomi, Kaishi [5 ]
Arinami, Tadao [1 ]
Hasegawa, Mamoru [6 ]
Fujioka, Tsuyoshi [7 ]
Nakamura, Yukio [7 ]
Noguchi, Emiko [1 ,8 ]
机构
[1] Univ Tsukuba, Fac Med, Dept Med Genet, Tsukuba, Ibaraki, Japan
[2] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21205 USA
[3] Univ Tsukuba, Dept Regenerat Med & Stem Cell Biol, Fac Med, Tsukuba, Ibaraki, Japan
[4] Univ Fukui, Fac Med Sci, Dept Otorhinolaryngol Head & Neck Surg, Fukui 910, Japan
[5] Univ Tsukuba, Dept Diagnost Pathol, Fac Med, Tsukuba, Ibaraki, Japan
[6] DNAVEC Res Inc, Tsukuba, Ibaraki, Japan
[7] RIKEN, BioResource Ctr, Cell Engn Div, Tsukuba, Ibaraki, Japan
[8] Japan Sci & Technol Agcy, Chiyoda Ku, Tokyo 1028666, Japan
来源
PLOS ONE | 2012年 / 7卷 / 08期
基金
日本科学技术振兴机构;
关键词
INDUCTION; DERIVATION;
D O I
10.1371/journal.pone.0042855
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The generation of induced pluripotent stem cells (iPSCs) by introducing reprogramming factors into somatic cells is a promising method for stem cell therapy in regenerative medicine. Therefore, it is desirable to develop a minimally invasive simple method to create iPSCs. In this study, we generated human nasal epithelial cells (HNECs)-derived iPSCs by gene transduction with Sendai virus (SeV) vectors. HNECs can be obtained from subjects in a noninvasive manner, without anesthesia or biopsy. In addition, SeV carries no risk of altering the host genome, which provides an additional level of safety during generation of human iPSCs. The multiplicity of SeV infection ranged from 3 to 4, and the reprogramming efficiency of HNECs was 0.08-0.10%. iPSCs derived from HNECs had global gene expression profiles and epigenetic states consistent with those of human embryonic stem cells. The ease with which HNECs can be obtained, together with their robust reprogramming characteristics, will provide opportunities to investigate disease pathogenesis and molecular mechanisms in vitro, using cells with particular genotypes.
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页数:7
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