A window of hope: Cell therapy using neural stem cells for neonatal brain injury

2021 ◽  
Vol 63 (1) ◽  
pp. 3-4
Author(s):  
Atsushi Uchiyama
2011 ◽  
Vol 70 (1) ◽  
pp. 3-9 ◽  
Author(s):  
Cesar V Borlongan ◽  
Michael D Weiss

2012 ◽  
Vol 26 ◽  
pp. S41
Author(s):  
C.T. van Velthoven ◽  
V. Donega ◽  
C.H. Nijboer ◽  
A. Kavelaars ◽  
C.J. Heijnen

2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
Xinxin Han ◽  
Liming Yu ◽  
Jie Ren ◽  
Min Wang ◽  
Zhongliang Liu ◽  
...  

Stem cell-based therapies have been used for repairing damaged brain tissue and helping functional recovery after brain injury. Aberrance neurogenesis is related with brain injury, and multipotential neural stem cells from human embryonic stem (hES) cells provide a great promise for cell replacement therapies. Optimized protocols for neural differentiation are necessary to produce functional human neural stem cells (hNSCs) for cell therapy. However, the qualified procedure is scarce and detailed features of hNSCs originated from hES cells are still unclear. In this study, we developed a method to obtain hNSCs from hES cells, by which we could harvest abundant hNSCs in a relatively short time. Then, we examined the expression of pluripotent and multipotent marker genes through immunostaining and confirmed differentiation potential of the differentiated hNSCs. Furthermore, we analyzed the mitotic activity of these hNSCs. In this report, we provided comprehensive features of hNSCs and delivered the knowledge about how to obtain more high-quality hNSCs from hES cells which may help to accelerate the NSC-based therapies in brain injury treatment.


2011 ◽  
Vol 70 (5) ◽  
pp. 698-712 ◽  
Author(s):  
Luigi Titomanlio ◽  
Annemieke Kavelaars ◽  
Jeremie Dalous ◽  
Shyamala Mani ◽  
Vincent El Ghouzzi ◽  
...  

2014 ◽  
Vol 41 (1) ◽  
pp. 133-148 ◽  
Author(s):  
Bobbi Fleiss ◽  
Pascale V. Guillot ◽  
Luigi Titomanlio ◽  
Olivier Baud ◽  
Henrik Hagberg ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
Xinxin Han ◽  
Liming Yu ◽  
Qingqing Chen ◽  
Min Wang ◽  
Jie Ren ◽  
...  

Monkeys are much closer to human and are the most common nonhuman primates which are used in biomedical studies. Neural progenitor cells can originate from the hippocampus of adult monkeys. Despite a few reports, the detailed properties of monkey neural stem cells (NSCs) and their responses to cytokine are still unclear. Here, we derive NSCs from an adult monkey brain and demonstrate that BMP4 inhibits cell proliferation and affects cell morphology of monkey NSCs. Combined treatment of BMP4 and LIF or RA and Forskolin represses the proliferation of monkey NSCs. We also show that BMP4 may promote monkey NSC quiescence. Our study therefore provides implications for NSC-based cell therapy of brain injury in the future.


Sign in / Sign up

Export Citation Format

Share Document