Glycosignaling in neural stem cells: involvement of glycoconjugates in signal transduction modulating the neural stem cell fate

2007 ◽  
Vol 103 (s1) ◽  
pp. 39-46 ◽  
Author(s):  
Robert K. Yu ◽  
Makoto Yanagisawa
2010 ◽  
Vol 30 (5) ◽  
pp. 403-408 ◽  
Author(s):  
Hyo-Jung Park ◽  
Jun-Kyum Kim ◽  
Hye-Min Jeon ◽  
Se-Yeong Oh ◽  
Sung-Hak Kim ◽  
...  

2011 ◽  
Vol 31 (2) ◽  
pp. 199-199 ◽  
Author(s):  
Hyo-Jung Park ◽  
Jun-Kyum Kim ◽  
Hye-Min Jeon ◽  
Se-Yeong Oh ◽  
Sung-Hak Kim ◽  
...  

2018 ◽  
Vol 44 ◽  
pp. S87
Author(s):  
J. Vasconcelos E Sá ◽  
D. Simão ◽  
M.M. Silva ◽  
A.P. Terrasso ◽  
I.A. Isidro ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Louis N. Manganas ◽  
Irene Durá ◽  
Sivan Osenberg ◽  
Faith Semerci ◽  
Mehmet Tosun ◽  
...  

AbstractThe mechanisms responsible for determining neural stem cell fate are numerous and complex. To begin to identify the specific components involved in these processes, we generated several mouse neural stem cell (NSC) antibodies against cultured mouse embryonic neurospheres. Our immunohistochemical data showed that the NSC-6 antibody recognized NSCs in the developing and postnatal murine brains as well as in human brain organoids. Mass spectrometry revealed the identity of the NSC-6 epitope as brain abundant, membrane-attached signal protein 1 (BASP1), a signaling protein that plays a key role in neurite outgrowth and plasticity. Western blot analysis using the NSC-6 antibody demonstrated multiple BASP1 isoforms with varying degrees of expression and correlating with distinct developmental stages. Herein, we describe the expression of BASP1 in NSCs in the developing and postnatal mammalian brains and human brain organoids, and demonstrate that the NSC-6 antibody may be a useful marker of these cells.


2018 ◽  
Vol 6 (4) ◽  
pp. 25 ◽  
Author(s):  
Katherine Harding ◽  
Kristin White

Stem cells face a diversity of choices throughout their lives. At specific times, they may decide to initiate cell division, terminal differentiation, or apoptosis, or they may enter a quiescent non-proliferative state. Neural stem cells in the Drosophila central nervous system do all of these, at stereotypical times and anatomical positions during development. Distinct populations of neural stem cells offer a unique system to investigate the regulation of a particular stem cell behavior, while comparisons between populations can lead us to a broader understanding of stem cell identity. Drosophila is a well-described and genetically tractable model for studying fundamental stem cell behavior and the mechanisms that underlie cell-fate decisions. This review will focus on recent advances in our understanding of the factors that contribute to distinct stem cell-fate decisions within the context of the Drosophila nervous system.


2006 ◽  
Vol 32 (2) ◽  
pp. 353-362 ◽  
Author(s):  
Lianhua Bai ◽  
Arnold Caplan ◽  
Donald Lennon ◽  
Robert H. Miller

2014 ◽  
Vol 21 (19) ◽  
pp. 2190-2207 ◽  
Author(s):  
S. Schildge ◽  
C. Bohrer ◽  
S. Pfurr ◽  
K. Mammadzada ◽  
K. Schachtrup ◽  
...  

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