Rapid and Efficient Direct Conversion of Human Adult Somatic Cells into Neural Stem Cells by HMGA2/let-7b

被引:79
|
作者
Yu, Kyung-Rok [1 ,2 ]
Shin, Ji-Hee [1 ,2 ]
Kim, Jae-Jun [1 ,2 ]
Koog, Myung Guen [1 ,2 ]
Lee, Jin Young [1 ,2 ]
Choi, Soon Won [1 ,2 ]
Kim, Hyung-Sik [1 ,2 ]
Seo, Yoojin [1 ,2 ]
Lee, SeungHee [1 ,2 ,3 ]
Shin, Tae-hoon [1 ,2 ]
Jee, Min Ki [1 ,2 ]
Kim, Dong-Wook [4 ]
Jung, Sung Jun [5 ]
Shin, Sue [6 ,7 ,8 ]
Han, Dong Wook
Kang, Kyung-Sun [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Vet Med, Adult Stem Cell Res Ctr, Seoul 151742, South Korea
[2] Seoul Natl Univ, Coll Vet Med, Res Inst Vet Sci, Seoul 151742, South Korea
[3] Seoul Natl Univ, Biotechnol Incubating Ctr, Inst Stem Cell & Regenerat Med Kang Stem Biotech, Seoul 151742, South Korea
[4] Yonsei Univ, Coll Med, Dept Physiol & Brain Korea Plus Project Med Sci 2, Seoul 120752, South Korea
[5] Hanyang Univ, Sch Med, Dept Physiol, Seoul 133791, South Korea
[6] Seoul Natl Univ, Coll Med, SMG SNU Boramae Med Ctr, Dept Lab Med, Seoul 156707, South Korea
[7] Seoul Metropolitan Publ Cord Blood Bank, Seoul 156707, South Korea
[8] Konkuk Univ, Sch Med, Dept Stem Cell Biol, Seoul 143701, South Korea
来源
CELL REPORTS | 2015年 / 10卷 / 03期
基金
新加坡国家研究基金会;
关键词
C-MYC; HUMAN FIBROBLASTS; HMGA PROTEINS; STROMAL CELLS; CHROMATIN; NEURONS; DIFFERENTIATION; PROLIFERATION; BIOLOGY; CANCER;
D O I
10.1016/j.celrep.2014.12.038
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A recent study has suggested that fibroblasts can be converted into mouse-induced neural stem cells (miNSCs) through the expression of defined factors. However, successful generation of human iNSCs (hiNSCs) has proven challenging to achieve. Here, using microRNA (miRNA) expression profile analyses, we showed that let-7 microRNA has critical roles for the formation of PAX6/NESTIN-positive colonies from human adult fibroblasts and the proliferation and self-renewal of hiNSCs. HMGA2, a let-7-targeting gene, enables induction of hiNSCs that displayed morphological/molecular features and in vitro/in vivo differentiation potential similar to H9-derived NSCs. Interestingly, HMGA2 facilitated the efficient conversion of senescent somatic cells or blood CD34+ cells into hiNSCs through an interaction with SOX2, whereas other combinations or SOX2 alone showed a limited conversion ability. Taken together, these findings suggest that HMGA2/let-7 facilitates direct reprogramming toward hiNSCs in minimal conditions and maintains hiNSC self-renewal, providing a strategy for the clinical treatment of neurological diseases.
引用
收藏
页码:441 / 452
页数:12
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