Reprogramming of murine and human somatic cells using a single polycistronic vector

被引:360
作者
Carey, Bryce W. [1 ,2 ]
Markoulaki, Styliani [1 ]
Hanna, Jacob [1 ]
Saha, Kris [1 ]
Gao, Qing [1 ]
Mitalipova, Maisam [1 ]
Jaenisch, Rudolf [1 ,2 ]
机构
[1] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
基金
美国国家卫生研究院;
关键词
2A peptide; four-factor reprogramming; iPS cell; polycistronic; PLURIPOTENT STEM-CELLS; FIBROBLASTS; GENERATION; EXPRESSION; CLEAVAGE; SYSTEM;
D O I
10.1073/pnas.0811426106
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
Directed reprogramming of somatic cells by defined factors provides a novel method for the generation of patient-specific stem cells with the potential to bypass both the practical and ethical concerns associated with somatic cell nuclear transfer (SCNT) and human embryonic stem (hES) cells. Although the generation of induced pluripotent stem (iPS) cells has proven a robust technology in mouse and human, a major impediment to the use of iPS cells for therapeutic purposes has been the viral-based delivery of the reprogramming factors because multiple proviral integrations pose the danger of insertional mutagenesis. Here we report a novel approach to reduce the number of viruses necessary to reprogram somatic cells by delivering reprogramming factors in a single virus using 2A "self- cleaving'' peptides, which support efficient polycistronic expression from a single promoter. We find that up to four reprogramming factors (Oct4, Sox2, Klf4, and c-Myc) can be expressed from a single virus to generate iPS cells in both embryonic and adult somatic mouse cells and we show that a single proviral copy is sufficient to generate iPS cells from mouse embryonic fibroblasts. In addition we have generated human induced pluripotent stem (hiPS) cell lines from human keratinocytes, demonstrating that a single polycistronic virus can reprogram human somatic cells.
引用
收藏
页码:157 / 162
页数:6
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