Signaling pathways of the early differentiation of neural stem cells by neurotrophin-3

2007 ◽  
Vol 357 (4) ◽  
pp. 903-909 ◽  
Author(s):  
Myung-Shin Lim ◽  
Sang-Hyun Nam ◽  
Sun-Jung Kim ◽  
Seog-Youn Kang ◽  
Yong-Soon Lee ◽  
...  
Cell Research ◽  
2008 ◽  
Vol 18 (S1) ◽  
pp. S59-S59
Author(s):  
Zhifeng Deng ◽  
Zhumin Liu ◽  
Wei Tu ◽  
Yang Wang ◽  
Yuanlei Lou

2016 ◽  
Vol 54 (8) ◽  
pp. 6213-6224 ◽  
Author(s):  
Nora Bengoa-Vergniory ◽  
Irantzu Gorroño-Etxebarria ◽  
Inmaculada López-Sánchez ◽  
Michele Marra ◽  
Pierluigi Di Chiaro ◽  
...  

2019 ◽  
Vol 28 (12) ◽  
pp. 1686-1699 ◽  
Author(s):  
Chongfeng Chen ◽  
Yujia Yang ◽  
Yue Yao

Hyperbaric oxygen (HBO) therapy may promote neurological recovery from hypoxic-ischemic encephalopathy (HIE). However, the therapeutic effects of HBO and its associated mechanisms remain unknown. The canonical Wnt/β-catenin signaling pathways and bone morphogenetic protein (BMP) play important roles in mammalian nervous system development. The present study examined whether HBO stimulates the differentiation of neural stem cells (NSCs) and its effect on Wnt3/β-catenin and BMP2 signaling pathways. We showed HBO treatment (2 ATA, 60 min) promoted differentiation of NSCs into neurons and oligodendrocytes in vitro. In addition, rat hypoxic-ischemic brain damage (HIBD) tissue extracts also promoted the differentiation of NSCs into neurons and oligodendrocytes, with the advantage of reducing the number of astrocytes. These effects were most pronounced when these two were combined together. In addition, the expression of Wnt3a, BMP2, and β-catenin nuclear proteins were increased after HBO treatment. However, blockade of Wnt/β-catenin or BMP signaling inhibited NSC differentiation and reduced the expression of Wnt3a, BMP2, and β-catenin nuclear proteins. In conclusion, HBO promotes differentiation of NSCs into neurons and oligodendrocytes and reduced the number of astrocytes in vitro possibly through regulation of Wnt3/β-catenin and BMP2 signaling pathways. HBO may serve as a potential therapeutic strategy for treating HIE.


PLoS ONE ◽  
2017 ◽  
Vol 12 (2) ◽  
pp. e0171359 ◽  
Author(s):  
Lei Wang ◽  
Yujia Deng ◽  
Da Duan ◽  
Shuaiqi Sun ◽  
Lite Ge ◽  
...  

PROTEOMICS ◽  
2008 ◽  
Vol 8 (21) ◽  
pp. 4547-4559 ◽  
Author(s):  
Helena Skalnikova ◽  
Petr Vodicka ◽  
Steven Pelech ◽  
Jan Motlik ◽  
Suresh Jivan Gadher ◽  
...  

Stem Cells ◽  
2014 ◽  
Vol 32 (12) ◽  
pp. 3196-3208 ◽  
Author(s):  
Nora Bengoa-Vergniory ◽  
Irantzu Gorroño-Etxebarria ◽  
Itxaso González-Salazar ◽  
Robert M. Kypta

2020 ◽  
Author(s):  
Kasum Azim ◽  
Filippo Calzolari ◽  
Martina Cantone ◽  
Rainer Akkermann ◽  
Julio Vera ◽  
...  

AbstractThe subventricular zone (SVZ) is the largest neurogenic niche in the adult forebrain. Notably, neural stem cells (NSCs) of the SVZ generate not only neurons, but also oligodendrocytes, the myelin-forming cells of the central nervous system. Transcriptomic studies have provided detailed knowledge of the molecular events that regulate neurogenesis, but little is understood about adult oligodendrogenesis from SVZ-NSCs. To address this, we performed in-depth single-cell transcriptomic analyses to resolve the major differences in neuronal and oligodendroglial lineages derived from the adult SVZ. A hallmark of adult oligodendrogenesis was the stage-specific expression of transcriptional modulators that regulate developmental oligodendrogenesis. Notably, divergence of the oligodendroglial lineage was distinguished by Wnt-Notch and angiogenesis-related signaling, whereas G-protein-coupled receptor signaling pathways were the major signature observed in the neurogenic lineage. Moreover, in-depth gene regulatory network analysis identified key stage-specific master regulators of the oligodendrocyte lineage and revealed new mechanisms by which signaling pathways interact with transcriptional networks to control lineage progression. Our work provides an integrated view of the multi-step differentiation process leading from NSCs to mature oligodendrocytes, by linking environmental signals to known and novel transcriptional mechanisms orchestrating oligodendrogenesis.Main pointsDistinct adult NSC populations giving rise to either oligodendrocytes or neurons can be identified by the expression of transcription factors.Gene regulatory control of oligodendrogenesis is a major fate-determinant for their generation.


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