Transcriptional regulatory networks associated with self-renewal and differentiation of neural stem cells

Neural stem cells (NSCs) are self‐renewing, multipotent cells that can generate neurons, astrocytes, and oligodendrocytes of the nervous system. NSCs have been extensively studied because they can be used to treat impaired cells and tissues or improve regenerative power of degenrating cells in neuro...

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Published in:Journal of cellular physiology Vol. 225; no. 2; pp. 337 - 347
Main Authors: Yun, So Jeong, Byun, Kyunghee, Bhin, Jinhyuk, Oh, Jee-Hyun, Nhung, Le Thi Hong, Hwang, Daehee, Lee, Bonghee
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-11-2010
Wiley Subscription Services, Inc
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Summary:Neural stem cells (NSCs) are self‐renewing, multipotent cells that can generate neurons, astrocytes, and oligodendrocytes of the nervous system. NSCs have been extensively studied because they can be used to treat impaired cells and tissues or improve regenerative power of degenrating cells in neurodegenerative diseases or spinal cord injuries. For successful clinical applications of NSCs, it is essential to understand the mechanisms underlying self‐renewal and differentiation of NSCs, which involve complex interplays among key factors including transcription factors, epigenetic control, microRNAs, and signaling pathways. Despite numerous studies on such factors, a holistic view of their interplays during neural development still remains elusive. In this review, we present recently identified potential regulatory factors and their targets by genomics and proteomics technologies and then integrate them into regulatory networks that describe their complex interplays to achieve self‐renewal and differentiation of NSCs. J. Cell. Physiol. 225: 337–347, 2010. © 2010 Wiley‐Liss, Inc.
Bibliography:ArticleID:JCP22294
ark:/67375/WNG-NWH2HF9K-Z
So Jeong Yun and Kyunghee Byun equally contributed to this work.
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ObjectType-Article-2
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ObjectType-Review-1
ISSN:0021-9541
1097-4652
DOI:10.1002/jcp.22294