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Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells

Glial-restricted precursor (GRP) cells, the earliest glial progenitors for both astrocytes and oligodendrocytes, have been derived from embryos and embryonic stem cells (ESC) in rodents. However, knowledge regarding the equivalent cell type in primates is limited due to restrictions imposed by ethic...

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Detalles Bibliográficos
Autores principales: Chen, Hongwei, Mao, Yu, Wang, Shufen, Li, Bin, Wang, Jinhuan, Li, Jian, Ma, Yuanye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter Open 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936634/
https://www.ncbi.nlm.nih.gov/pubmed/28123809
http://dx.doi.org/10.1515/tnsci-2015-0026
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author Chen, Hongwei
Mao, Yu
Wang, Shufen
Li, Bin
Wang, Jinhuan
Li, Jian
Ma, Yuanye
author_facet Chen, Hongwei
Mao, Yu
Wang, Shufen
Li, Bin
Wang, Jinhuan
Li, Jian
Ma, Yuanye
author_sort Chen, Hongwei
collection PubMed
description Glial-restricted precursor (GRP) cells, the earliest glial progenitors for both astrocytes and oligodendrocytes, have been derived from embryos and embryonic stem cells (ESC) in rodents. However, knowledge regarding the equivalent cell type in primates is limited due to restrictions imposed by ethics and resources. Here we report successful derivation and characterization of primate GRP cells from rhesus monkey ESC. The purified monkey GRP cells were A(2)B(5)-positive and FGF2-dependent for survival and proliferation. The differentiation assays indicated that they were tri-potential in vitro and bi-potential in vivo. These newly purified GRP cells will help to facilitate understanding of the molecular mechanism of glial development in primates as well as provide a source of therapeutic donor cells for use in neuroregenerative medicine.
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spelling pubmed-49366342017-01-25 Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells Chen, Hongwei Mao, Yu Wang, Shufen Li, Bin Wang, Jinhuan Li, Jian Ma, Yuanye Transl Neurosci Research Article Glial-restricted precursor (GRP) cells, the earliest glial progenitors for both astrocytes and oligodendrocytes, have been derived from embryos and embryonic stem cells (ESC) in rodents. However, knowledge regarding the equivalent cell type in primates is limited due to restrictions imposed by ethics and resources. Here we report successful derivation and characterization of primate GRP cells from rhesus monkey ESC. The purified monkey GRP cells were A(2)B(5)-positive and FGF2-dependent for survival and proliferation. The differentiation assays indicated that they were tri-potential in vitro and bi-potential in vivo. These newly purified GRP cells will help to facilitate understanding of the molecular mechanism of glial development in primates as well as provide a source of therapeutic donor cells for use in neuroregenerative medicine. De Gruyter Open 2015-11-27 /pmc/articles/PMC4936634/ /pubmed/28123809 http://dx.doi.org/10.1515/tnsci-2015-0026 Text en © 2015 Hongwei Chen et al. licensee De Gruyter Open. http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.
spellingShingle Research Article
Chen, Hongwei
Mao, Yu
Wang, Shufen
Li, Bin
Wang, Jinhuan
Li, Jian
Ma, Yuanye
Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells
title Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells
title_full Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells
title_fullStr Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells
title_full_unstemmed Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells
title_short Characterization of glial-restricted precursors from rhesus monkey embryonic stem cells
title_sort characterization of glial-restricted precursors from rhesus monkey embryonic stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936634/
https://www.ncbi.nlm.nih.gov/pubmed/28123809
http://dx.doi.org/10.1515/tnsci-2015-0026
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