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Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet

BACKGROUND: The porcine brain is gyrencephalic with similar gray and white matter composition and size more comparable to the human rather than the rodent brain; however, there is lack of information about neural progenitor cells derived from this model. RESULTS: Here, we isolated GFAP-positive porc...

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Autores principales: Kim, Eunhye, Hwang, Seon-Ung, Yoon, Junchul David, Kim, Hyunggee, Lee, Gabsang, Hyun, Sang-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222979/
https://www.ncbi.nlm.nih.gov/pubmed/30404643
http://dx.doi.org/10.1186/s12917-018-1660-4
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author Kim, Eunhye
Hwang, Seon-Ung
Yoon, Junchul David
Kim, Hyunggee
Lee, Gabsang
Hyun, Sang-Hwan
author_facet Kim, Eunhye
Hwang, Seon-Ung
Yoon, Junchul David
Kim, Hyunggee
Lee, Gabsang
Hyun, Sang-Hwan
author_sort Kim, Eunhye
collection PubMed
description BACKGROUND: The porcine brain is gyrencephalic with similar gray and white matter composition and size more comparable to the human rather than the rodent brain; however, there is lack of information about neural progenitor cells derived from this model. RESULTS: Here, we isolated GFAP-positive porcine neural stem cells (NSCs) from the brain explant of a transgenic piglet, with expression of CreER(T2) under the control of the GFAP promoter (pGFAP-CreER(T2)). The isolated pGFAP-CreER(T2) NSCs showed self-renewal and expression of representative NSC markers such as Nestin and Sox2. Pharmacological inhibition studies revealed that Notch1 signaling is necessary to maintain NSC identity, whereas serum treatment induced cell differentiation into reactive astrocytes and neurons. CONCLUSIONS: Collectively, these results indicate that GFAP promoter-driven porcine CreER(T2) NSCs would be a useful tool to study neurogenesis of the porcine adult central nervous system and furthers our understanding of its potential clinical application in the future. GRAPHICAL ABSTRACT: ᅟ [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-018-1660-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-62229792018-11-19 Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet Kim, Eunhye Hwang, Seon-Ung Yoon, Junchul David Kim, Hyunggee Lee, Gabsang Hyun, Sang-Hwan BMC Vet Res Research Article BACKGROUND: The porcine brain is gyrencephalic with similar gray and white matter composition and size more comparable to the human rather than the rodent brain; however, there is lack of information about neural progenitor cells derived from this model. RESULTS: Here, we isolated GFAP-positive porcine neural stem cells (NSCs) from the brain explant of a transgenic piglet, with expression of CreER(T2) under the control of the GFAP promoter (pGFAP-CreER(T2)). The isolated pGFAP-CreER(T2) NSCs showed self-renewal and expression of representative NSC markers such as Nestin and Sox2. Pharmacological inhibition studies revealed that Notch1 signaling is necessary to maintain NSC identity, whereas serum treatment induced cell differentiation into reactive astrocytes and neurons. CONCLUSIONS: Collectively, these results indicate that GFAP promoter-driven porcine CreER(T2) NSCs would be a useful tool to study neurogenesis of the porcine adult central nervous system and furthers our understanding of its potential clinical application in the future. GRAPHICAL ABSTRACT: ᅟ [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-018-1660-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-07 /pmc/articles/PMC6222979/ /pubmed/30404643 http://dx.doi.org/10.1186/s12917-018-1660-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kim, Eunhye
Hwang, Seon-Ung
Yoon, Junchul David
Kim, Hyunggee
Lee, Gabsang
Hyun, Sang-Hwan
Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet
title Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet
title_full Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet
title_fullStr Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet
title_full_unstemmed Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet
title_short Isolation and characterization of GFAP-positive porcine neural stem/progenitor cells derived from a GFAP-CreER(T2) transgenic piglet
title_sort isolation and characterization of gfap-positive porcine neural stem/progenitor cells derived from a gfap-creer(t2) transgenic piglet
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222979/
https://www.ncbi.nlm.nih.gov/pubmed/30404643
http://dx.doi.org/10.1186/s12917-018-1660-4
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