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

Authors
Yu, Kyung-RokShin, Ji-HeeKim, Jae-JunKoog, Myung GuenLee, Jin YoungChoi, Soon WonKim, Hyung-SikSeo, YoojinLee, SeungHeeShin, Tae-hoonJee, Min KiKim, Dong-WookJung, Sung JunShin, SueHan, Dong WookKang, Kyung-Sun
Issue Date
Jan-2015
Publisher
CELL PRESS
Citation
CELL REPORTS, v.10, no.3, pp.441 - 452
Indexed
SCIE
SCOPUS
Journal Title
CELL REPORTS
Volume
10
Number
3
Start Page
441
End Page
452
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/158180
DOI
10.1016/j.celrep.2014.12.038
ISSN
2211-1247
Abstract
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.
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