Yu Kyung-Rok, Shin Ji-Hee, Kim Jae-Jun, Koog Myung Guen, Lee Jin Young, Choi Soon Won, Kim Hyung-Sik, Seo Yoojin, Lee SeungHee, Shin Tae-Hoon, Jee Min Ki, Kim Dong-Wook, Jung Sung Jun, Shin Sue, Han Dong Wook, Kang Kyung-Sun
Adult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea; The Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea.
Adult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea; The Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea; Institute for Stem Cell and Regenerative Medicine in Kang Stem Biotech, Biotechnology Incubating Center, Seoul National University, Seoul 151-742, Korea.
Cell Rep. 2015 Jan 20;10(3):441-452. doi: 10.1016/j.celrep.2014.12.038. Epub 2015 Jan 15.
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.
最近的一项研究表明,通过表达特定因子,成纤维细胞可转化为小鼠诱导神经干细胞(miNSCs)。然而,已证明成功生成人类诱导神经干细胞(hiNSCs)具有挑战性。在此,我们通过微小RNA(miRNA)表达谱分析表明,let-7微小RNA对于从人类成纤维细胞形成PAX6/NESTIN阳性集落以及hiNSCs的增殖和自我更新起着关键作用。HMGA2是一个受let-7靶向的基因,能够诱导出具有与H9来源的神经干细胞相似的形态/分子特征以及体外/体内分化潜能的hiNSCs。有趣的是,HMGA2通过与SOX2相互作用,促进衰老体细胞或血液CD34+细胞高效转化为hiNSCs,而其他组合或单独的SOX2显示出有限的转化能力。综上所述,这些发现表明HMGA2/let-7在最小条件下促进向hiNSCs的直接重编程并维持hiNSC自我更新,为神经疾病的临床治疗提供了一种策略。