The bHLH Transcription Factors in Neural Development and Therapeutic Applications for Neurodegenerative Diseases

被引:8
作者
Lee, Dong Gi [1 ]
Kim, Young-Kwang [2 ]
Baek, Kwang-Hyun [2 ]
机构
[1] Univ Ghent, Joint Sect Sci Environm Technol Food Technol & Mo, Incheon 21569, South Korea
[2] CHA Univ, CHA Stem Cell Inst, Dept Biomed Sci, Seongnam 13488, South Korea
基金
新加坡国家研究基金会;
关键词
AtN conversion; basic helix-loop-helix; cell therapy; gene therapy; iPSC; reprogramming; TRANsCre-DIONE; transdifferentiation; tunneling nanotubes; FUNCTIONAL-NEURONS; STEM-CELLS; IN-VITRO; FACTOR OLIG2; DIRECTED DIFFERENTIATION; NEGATIVE AUTOREGULATION; DOPAMINERGIC-NEURONS; DETERMINATION GENES; PARKINSONS-DISEASE; SIGNALING PATHWAY;
D O I
10.3390/ijms232213936
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of functional neural circuits in the central nervous system (CNS) requires the production of sufficient numbers of various types of neurons and glial cells, such as astrocytes and oligodendrocytes, at the appropriate periods and regions. Hence, severe neuronal loss of the circuits can cause neurodegenerative diseases such as Huntington's disease (HD), Parkinson's disease (PD), Alzheimer's disease (AD), and Amyotrophic Lateral Sclerosis (ALS). Treatment of such neurodegenerative diseases caused by neuronal loss includes some strategies of cell therapy employing stem cells (such as neural progenitor cells (NPCs)) and gene therapy through cell fate conversion. In this report, we review how bHLH acts as a regulator in neuronal differentiation, reprogramming, and cell fate determination. Moreover, several different researchers are conducting studies to determine the importance of bHLH factors to direct neuronal and glial cell fate specification and differentiation. Therefore, we also investigated the limitations and future directions of conversion or transdifferentiation using bHLH factors.
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页数:18
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