The Future Vocation of Neural Stem Cells: Lineage Commitment in Brain Development and Evolution

2018 ◽  
Vol 43 (1) ◽  
pp. 162-165 ◽  
Author(s):  
Tadashi Nomura ◽  
Hitoshi Gotoh ◽  
Katsuhiko Ono
Author(s):  
Patricia P Garcez ◽  
Erick C Loiola ◽  
Rodrigo F Madeiro da Costa ◽  
Luiza Higa ◽  
Pablo Trindade ◽  
...  

Since the emergence of Zika virus (ZIKV), reports of microcephaly have increased dramatically in Brazil; however, causality between the widespread epidemic and malformations in fetal brains has not been confirmed. Here, we examine the effects of ZIKV infection in human neural stem cells growing as neurospheres and cerebral organoids. Using immunocytochemistry and electron microscopy, we show that ZIKV targets human brain cells, reducing their viability and growth as neurospheres and cerebral organoids. These results suggest that ZIKV abrogates neurogenesis during human brain development.


Author(s):  
Patricia P Garcez ◽  
Erick C Loiola ◽  
Rodrigo F Madeiro da Costa ◽  
Luiza Higa ◽  
Pablo Trindade ◽  
...  

Since the emergence of Zika virus (ZIKV), reports of microcephaly have increased dramatically in Brazil; however, causality between the widespread epidemic and malformations in fetal brains has not been confirmed. Here, we examine the effects of ZIKV infection in human neural stem cells growing as neurospheres and cerebral organoids. Using immunocytochemistry and electron microscopy, we show that ZIKV targets human brain cells, reducing their viability and growth as neurospheres and cerebral organoids. These results suggest that ZIKV abrogates neurogenesis during human brain development.


2013 ◽  
Vol 450 (3) ◽  
pp. 459-468 ◽  
Author(s):  
Ruopeng Feng ◽  
Shixin Zhou ◽  
Yinan Liu ◽  
Daijun Song ◽  
Zhilin Luan ◽  
...  

The transcription factor Sox2 [SRY (sex-determining region Y)-box 2] is essential for the regulation of self-renewal and homoeostasis of NSCs (neural stem cells) during brain development. However, the downstream targets of Sox2 and its underlying molecular mechanism are largely unknown. In the present study, we found that Sox2 directly up-regulates the expression of survivin, which inhibits the mitochondria-dependent apoptotic pathway in NSCs. Although overexpression of Sox2 elevates survivin expression, knockdown of Sox2 results in a decrease in survivin expression, thereby initiating the mitochondria-dependent apoptosis related to caspase 9 activation. Furthermore, cell apoptosis owing to knockdown of Sox2 can be rescued by ectopically expressing survivin in NSCs as well as in the mouse brain, as demonstrated by an in utero-injection approach. In short, we have found a novel Sox2/survivin pathway that regulates NSC survival and homoeostasis, thus revealing a new mechanism of brain development, neurological degeneration and such aging-related disorders.


2019 ◽  
Vol 29 (18) ◽  
pp. 2993-3005.e9 ◽  
Author(s):  
Diana Vargas-Hurtado ◽  
Jean-Baptiste Brault ◽  
Tristan Piolot ◽  
Ludovic Leconte ◽  
Nathalie Da Silva ◽  
...  

IBRO Reports ◽  
2019 ◽  
Vol 6 ◽  
pp. S7
Author(s):  
Fumio Matsuzaki ◽  
Ikumi Fujita ◽  
Atsunori Shitamukai ◽  
Fumiya Kusumoto ◽  
Shun Mase ◽  
...  

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