scholarly journals The Basic Helix-Loop-Helix Genes Hesr1/Hey1 and Hesr2/Hey2 Regulate Maintenance of Neural Precursor Cells in the Brain

2003 ◽  
Vol 278 (45) ◽  
pp. 44808-44815 ◽  
Author(s):  
Masami Sakamoto ◽  
Hiromi Hirata ◽  
Toshiyuki Ohtsuka ◽  
Yasumasa Bessho ◽  
Ryoichiro Kageyama
Stem Cells ◽  
2008 ◽  
Vol 26 (7) ◽  
pp. 1673-1682 ◽  
Author(s):  
Christine Rampon ◽  
Nicolas Weiss ◽  
Cyrille Deboux ◽  
Nathalie Chaverot ◽  
Florence Miller ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Yu Jiao ◽  
Björn Palmgren ◽  
Ekaterina Novozhilova ◽  
Ulrica Englund Johansson ◽  
Anne L. Spieles-Engemann ◽  
...  

Objectives. To study possible nerve regeneration of a damaged auditory nerve by the use of stem cell transplantation.Methods. We transplanted HNPCs to the rat AN trunk by the internal auditory meatus (IAM). Furthermore, we studied if addition of BDNF affects survival and phenotypic differentiation of the grafted HNPCs. A bioactive nanofiber gel (PA gel), in selected groups mixed with BDNF, was applied close to the implanted cells. Before transplantation, all rats had been deafened by a round window niche application ofβ-bungarotoxin. This neurotoxin causes a selective toxic destruction of the AN while keeping the hair cells intact.Results. Overall, HNPCs survived well for up to six weeks in all groups. However, transplants receiving the BDNF-containing PA gel demonstrated significantly higher numbers of HNPCs and neuronal differentiation. At six weeks, a majority of the HNPCs had migrated into the brain stem and differentiated. Differentiated human cells as well as neurites were observed in the vicinity of the cochlear nucleus.Conclusion. Our results indicate that human neural precursor cells (HNPC) integration with host tissue benefits from additional brain derived neurotrophic factor (BDNF) treatment and that these cells appear to be good candidates for further regenerative studies on the auditory nerve (AN).


2018 ◽  
Vol 78 (4) ◽  
pp. 374-390
Author(s):  
Keiu Kask ◽  
Laura Tikker ◽  
Katrin Ruisu ◽  
Sirje Lulla ◽  
Eva-Maria Oja ◽  
...  

2019 ◽  
Vol 3 (2) ◽  
Author(s):  
Paul J. Lucassen ◽  
Anne-Marie van Dam ◽  
Prasanna Kandel ◽  
Pascal Bielefeld ◽  
Aniko Korosi ◽  
...  

Abstract Neuroinflammation and neurogenesis have both been the subject of intensive investigation over the past 20 years. The sheer complexity of their regulation and their ubiquity in various states of health and disease have sometimes obscured the progress that has been made in unraveling their mechanisms and regulation. A recent study by Kozareva et al. (Neuronal Signaling (2019) 3), provides evidence that the orphan nuclear receptor TLX is central to communication between microglia and neural precursor cells and could help us understand how inflammation, mediated by microglia, influences the development of new neurons in the adult hippocampus. Here, we put recent studies on TLX into the context of what is known about adult neurogenesis and microglial activation in the brain, along with the many hints that these processes must be inter-related.


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