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A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells

Small molecule compounds promoting the neuronal differentiation of stem/progenitor cells are of pivotal importance to regenerative medicine. We carried out a high-content screen to systematically characterize known bioactive compounds, on their effects on the neuronal differentiation and the midbrai...

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Autores principales: Rhim, Ji heon, Luo, Xiangjian, Xu, Xiaoyun, Gao, Dongbing, Zhou, Tieling, Li, Fuhai, Qin, Lidong, Wang, Ping, Xia, Xiaofeng, Wong, Stephen T. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635364/
https://www.ncbi.nlm.nih.gov/pubmed/26542303
http://dx.doi.org/10.1038/srep16237
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author Rhim, Ji heon
Luo, Xiangjian
Xu, Xiaoyun
Gao, Dongbing
Zhou, Tieling
Li, Fuhai
Qin, Lidong
Wang, Ping
Xia, Xiaofeng
Wong, Stephen T. C.
author_facet Rhim, Ji heon
Luo, Xiangjian
Xu, Xiaoyun
Gao, Dongbing
Zhou, Tieling
Li, Fuhai
Qin, Lidong
Wang, Ping
Xia, Xiaofeng
Wong, Stephen T. C.
author_sort Rhim, Ji heon
collection PubMed
description Small molecule compounds promoting the neuronal differentiation of stem/progenitor cells are of pivotal importance to regenerative medicine. We carried out a high-content screen to systematically characterize known bioactive compounds, on their effects on the neuronal differentiation and the midbrain dopamine (mDA) neuron specification of neural progenitor cells (NPCs) derived from the ventral mesencephalon of human fetal brain. Among the promoting compounds three major pharmacological classes were identified including the statins, TGF-βRI inhibitors, and GSK-3 inhibitors. The function of each class was also shown to be distinct, either to promote both the neuronal differentiation and mDA neuron specification, or selectively the latter, or promote the former but suppress the latter. We then carried out initial investigation on the possible mechanisms underlying, and demonstrated their applications on NPCs derived from human pluripotent stem cells (PSCs). Our study revealed the potential of several small molecule compounds for use in the directed differentiation of human NPCs. The screening result also provided insight into the signaling network regulating the differentiation of human NPCs.
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spelling pubmed-46353642015-11-25 A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells Rhim, Ji heon Luo, Xiangjian Xu, Xiaoyun Gao, Dongbing Zhou, Tieling Li, Fuhai Qin, Lidong Wang, Ping Xia, Xiaofeng Wong, Stephen T. C. Sci Rep Article Small molecule compounds promoting the neuronal differentiation of stem/progenitor cells are of pivotal importance to regenerative medicine. We carried out a high-content screen to systematically characterize known bioactive compounds, on their effects on the neuronal differentiation and the midbrain dopamine (mDA) neuron specification of neural progenitor cells (NPCs) derived from the ventral mesencephalon of human fetal brain. Among the promoting compounds three major pharmacological classes were identified including the statins, TGF-βRI inhibitors, and GSK-3 inhibitors. The function of each class was also shown to be distinct, either to promote both the neuronal differentiation and mDA neuron specification, or selectively the latter, or promote the former but suppress the latter. We then carried out initial investigation on the possible mechanisms underlying, and demonstrated their applications on NPCs derived from human pluripotent stem cells (PSCs). Our study revealed the potential of several small molecule compounds for use in the directed differentiation of human NPCs. The screening result also provided insight into the signaling network regulating the differentiation of human NPCs. Nature Publishing Group 2015-11-06 /pmc/articles/PMC4635364/ /pubmed/26542303 http://dx.doi.org/10.1038/srep16237 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Rhim, Ji heon
Luo, Xiangjian
Xu, Xiaoyun
Gao, Dongbing
Zhou, Tieling
Li, Fuhai
Qin, Lidong
Wang, Ping
Xia, Xiaofeng
Wong, Stephen T. C.
A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells
title A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells
title_full A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells
title_fullStr A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells
title_full_unstemmed A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells
title_short A High-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells
title_sort high-content screen identifies compounds promoting the neuronal differentiation and the midbrain dopamine neuron specification of human neural progenitor cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635364/
https://www.ncbi.nlm.nih.gov/pubmed/26542303
http://dx.doi.org/10.1038/srep16237
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