Mir-29b Mediates the Neural Tube versus Neural Crest Fate Decision during Embryonic Stem Cell Neural Differentiation

被引:23
|
作者
Xi, Jiajie [1 ]
Wu, Yukang [1 ]
Li, Guoping [1 ]
Ma, Li [1 ]
Feng, Ke [1 ]
Guo, Xudong [1 ]
Jia, Wenwen [1 ]
Wang, Guiying [1 ]
Yang, Guang [1 ]
Li, Ping [1 ]
Kang, Jiuhong [1 ,2 ]
机构
[1] Tongji Univ, Clin & Translat Res Ctr, Shanghai Matern & Infant Hlth Hosp 1, Shanghai Key Lab Signaling & Dis Res,Sch Life Sci, 1239 Siping Rd, Shanghai 200092, Peoples R China
[2] Tongji Univ, Collaborat Innovat Ctr Brain Sci, Shanghai 200092, Peoples R China
来源
STEM CELL REPORTS | 2017年 / 9卷 / 02期
基金
中国国家自然科学基金;
关键词
DIRECTED DIFFERENTIATION; GENE; TRANSCRIPTION; TARGET; LOOP; NEUROGENESIS; PRECURSORS; PROMOTERS; INDUCTION; MICRORNAS;
D O I
10.1016/j.stemcr.2017.06.017
中图分类号
Q813 [细胞工程];
学科分类号
摘要
During gastrulation, the neuroectoderm cells form the neural tube and neural crest. The nervous system contains significantlymore microRNAs than other tissues, but the role of microRNAs in controlling the differentiation of neuroectodermal cells into neural tube epithelial (NTE) cells and neural crest cells (NCCs) remains unknown. Using embryonic stem cell (ESC) neural differentiation systems, we found that miR-29b was upregulated in NTE cells and downregulated in NCCs. MiR-29b promoted the differentiation of ESCs into NTE cells and inhibited their differentiation into NCCs. Accordingly, the inhibition of miR-29b significantly inhibited the differentiation of NTE cells. A mechanistic study revealed that miR-29b targets DNA methyltransferase 3a (Dnmt3a) to regulate neural differentiation. Moreover, miR-29b mediated the function of Pou3f1, a critical neural transcription factor. Therefore, our study showed that the Pou3f1-miR-29b-Dnmt3a regulatory axis was active at the initial stage of neural differentiation and regulated the determination of cell fate.
引用
收藏
页码:571 / 586
页数:16
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