Mechanistic Insights Into MicroRNA-Induced Neuronal Reprogramming of Human Adult Fibroblasts

被引:24
|
作者
Lu, Ya-Lin [1 ,2 ]
Yoo, Andrew S. [1 ]
机构
[1] Washington Univ St Louis, Dept Dev Biol, Sch Med, St Louis, MO 63130 USA
[2] Washington Univ St Louis, Program Dev Regenerat & Stem Cell Biol, Sch Med, St Louis, MO USA
来源
FRONTIERS IN NEUROSCIENCE | 2018年 / 12卷
关键词
microRNA; chromatin; neuronal conversion; reprogramming; neurogenesis; disease modeling; human neurons; CHROMATIN REMODELING COMPLEX; TOPOISOMERASE II-BETA; PIONEER TRANSCRIPTION FACTORS; CELL FATE DECISIONS; NEURAL DEVELOPMENT; DIRECT CONVERSION; IN-VIVO; CORTICOFUGAL NEURONS; SEROTONERGIC NEURONS; FUNCTIONAL-NEURONS;
D O I
10.3389/fnins.2018.00522
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The use of transcriptional factors as cell fate regulators are often the primary focus in the direct reprogramming of somatic cells into neurons. However, in human adult fibroblasts, deriving functionally mature neurons with high efficiency requires additional neurogenic factors such as microRNAs (miRNAs) to evoke a neuronal state permissive to transcription factors to exert their reprogramming activities. As such, increasing evidence suggests brain-enriched miRNAs, miR-9/9* and miR-124, as potent neurogenic molecules through simultaneously targeting of anti-neurogenic effectors while allowing additional transcription factors to generate specific subtypes of human neurons. In this review, we will focus on methods that utilize neuronal miRNAs and provide mechanistic insights by which neuronal miRNAs, in synergism with brainregion specific transcription factors, drive the conversion of human fibroblasts into clinically relevant subtypes of neurons. Furthermore, we will provide insights into the age signature of directly converted neurons and how the converted human neurons can be utilized to model late-onset neurodegenerative disorders.
引用
收藏
页数:9
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