scholarly journals Proliferation and differentiation of human fetal brain neural stem cells in vitro

2018 ◽  
Vol Volume 6 ◽  
pp. 19-27 ◽  
Author(s):  
Erica McGrath ◽  
Junling Gao ◽  
Ping Wu
2014 ◽  
Vol 38 (1) ◽  
pp. 74-78 ◽  
Author(s):  
Shuang‐Qing Chen ◽  
Qing Cai ◽  
Yu‐Ying Shen ◽  
Xiu‐Ying Cai ◽  
Hai‐Ying Lei

2014 ◽  
Vol 92 (5) ◽  
pp. 574-586 ◽  
Author(s):  
Zhen Wang ◽  
Dexiang Liu ◽  
Qun Zhang ◽  
Jianmei Wang ◽  
Jingmin Zhan ◽  
...  

2008 ◽  
Vol 28 (6) ◽  
pp. 833-845 ◽  
Author(s):  
Nobutaka Horie ◽  
Kenji So ◽  
Takahiro Moriya ◽  
Naoki Kitagawa ◽  
Keisuke Tsutsumi ◽  
...  

2019 ◽  
Vol 29 (5) ◽  
pp. 727-735 ◽  
Author(s):  
Yuhang Cao ◽  
Yingliang Zhuang ◽  
Junchen Chen ◽  
Weize Xu ◽  
Yikai Shou ◽  
...  

Abstract N 6-methyladenosine (m6A) modification of RNA is deposited by the methyltransferase complex consisting of Mettl3 and Mettl14 and erased by demethylase Fto and Alkbh5 and is involved in diverse biological processes. However, it remains largely unknown the specific function and mechanism of Fto in regulating adult neural stem cells (aNSCs). In the present study, utilizing a conditional knockout (cKO) mouse model, we show that the specific ablation of Fto in aNSCs transiently increases the proliferation of aNSCs and promotes neuronal differentiation both in vitro and in vivo, but in a long term, the specific ablation of Fto inhibits adult neurogenesis and neuronal development. Mechanistically, Fto deficiency results in a significant increase in m6A modification in Pdgfra and Socs5. The increased expression of Pdgfra and decreased expression of Socs5 synergistically promote the phosphorylation of Stat3. The modulation of Pdgfra and Socs5 can rescue the neurogenic deficits induced by Fto depletion. Our results together reveal an important function of Fto in regulating aNSCs through modulating Pdgfra/Socs5-Stat3 pathway.


2017 ◽  
Vol 8 (3) ◽  
pp. 715-727 ◽  
Author(s):  
Erica L. McGrath ◽  
Shannan L. Rossi ◽  
Junling Gao ◽  
Steven G. Widen ◽  
Auston C. Grant ◽  
...  

2011 ◽  
Vol 51 (1) ◽  
pp. 104-112 ◽  
Author(s):  
Jie Fu ◽  
Shi-Dou Zhao ◽  
Hui-Juan Liu ◽  
Qiu-Huan Yuan ◽  
Shang-Ming Liu ◽  
...  

2019 ◽  
Author(s):  
Disha Sood ◽  
Dana M. Cairns ◽  
Jayanth M. Dabbi ◽  
Charu Ramakrishnan ◽  
Karl Deisseroth ◽  
...  

AbstractBrain extracellular matrix (ECM) is often overlooked in vitro brain tissue models, despite its instructive roles during development. Using developmental stage-sourced brain ECM in reproducible 3D bioengineered culture systems, we demonstrate enhanced functional differentiation of human induced neural stem cells (hiNSCs) into healthy neurons and astrocytes. Particularly, fetal brain tissue-derived ECM supported long-term maintenance of differentiated neurons, demonstrated by morphology, gene expression and secretome profiling. Astrocytes were evident within the second month of differentiation, and reactive astrogliosis was inhibited in brain ECM-enriched cultures when compared to unsupplemented cultures. Functional maturation of the differentiated hiNSCs within fetal ECM-enriched cultures was confirmed by calcium signaling and unsupervised cluster analysis. Additionally, the study identified native biochemical cues in decellularized ECM with notable comparisons between fetal and adult brain-derived ECMs. The development of novel brain-specific biomaterials for generating mature in vitro brain models provides an important path forward for interrogation of neuron-glia interactions.


Sign in / Sign up

Export Citation Format

Share Document