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Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia
Inferior colliculus (IC) is a major center for the integration and processing of acoustic information from ascending auditory pathways. Damage to the IC as well as normal aging can impair auditory function. Novel strategies such as stem cell (SC)-based regenerative therapy are required for functiona...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5948249/ https://www.ncbi.nlm.nih.gov/pubmed/28795331 http://dx.doi.org/10.1007/s12035-017-0701-5 |
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author | Okazaki, Haruka Kanda, Akira Kanda, Seiji Shimono, Takaki Yun, Yasutaka Kobayashi, Yoshiki Wang, Zeyun Ooka, Hisashi Suzuki, Kensuke Van, Dan Bui Tomoda, Koichi Iwai, Hiroshi Nishiyama, Toshimasa |
author_facet | Okazaki, Haruka Kanda, Akira Kanda, Seiji Shimono, Takaki Yun, Yasutaka Kobayashi, Yoshiki Wang, Zeyun Ooka, Hisashi Suzuki, Kensuke Van, Dan Bui Tomoda, Koichi Iwai, Hiroshi Nishiyama, Toshimasa |
author_sort | Okazaki, Haruka |
collection | PubMed |
description | Inferior colliculus (IC) is a major center for the integration and processing of acoustic information from ascending auditory pathways. Damage to the IC as well as normal aging can impair auditory function. Novel strategies such as stem cell (SC)-based regenerative therapy are required for functional recovery because mature neural cells have a minimal regenerative capacity after an injury. However, it is not known if there are neural stem cells (NSCs) in the IC. Herein, we screened for NSCs by surface marker analysis using flow cytometry. Isolated IC cells expressing prominin-1 (CD133) exhibited the cardinal NSC properties self-renewal capacity, expression of known NSC markers (SOX2 and nestin), and multipotency. Prominin-1-expressing cells from neonatal IC generated neurospheres, and culture of these neurospheres in differentiation-conditioned medium gave rise to gamma-aminobutyric acid-ergic (GABAergic) neurons, astrocytes, and oligodendrocytes. The presence of NSC-like cells in the IC has important implications for understanding IC development and for potential regenerative therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12035-017-0701-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5948249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-59482492018-05-17 Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia Okazaki, Haruka Kanda, Akira Kanda, Seiji Shimono, Takaki Yun, Yasutaka Kobayashi, Yoshiki Wang, Zeyun Ooka, Hisashi Suzuki, Kensuke Van, Dan Bui Tomoda, Koichi Iwai, Hiroshi Nishiyama, Toshimasa Mol Neurobiol Article Inferior colliculus (IC) is a major center for the integration and processing of acoustic information from ascending auditory pathways. Damage to the IC as well as normal aging can impair auditory function. Novel strategies such as stem cell (SC)-based regenerative therapy are required for functional recovery because mature neural cells have a minimal regenerative capacity after an injury. However, it is not known if there are neural stem cells (NSCs) in the IC. Herein, we screened for NSCs by surface marker analysis using flow cytometry. Isolated IC cells expressing prominin-1 (CD133) exhibited the cardinal NSC properties self-renewal capacity, expression of known NSC markers (SOX2 and nestin), and multipotency. Prominin-1-expressing cells from neonatal IC generated neurospheres, and culture of these neurospheres in differentiation-conditioned medium gave rise to gamma-aminobutyric acid-ergic (GABAergic) neurons, astrocytes, and oligodendrocytes. The presence of NSC-like cells in the IC has important implications for understanding IC development and for potential regenerative therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12035-017-0701-5) contains supplementary material, which is available to authorized users. Springer US 2017-08-09 2018 /pmc/articles/PMC5948249/ /pubmed/28795331 http://dx.doi.org/10.1007/s12035-017-0701-5 Text en © The Author(s) 2017 Open Access This 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. |
spellingShingle | Article Okazaki, Haruka Kanda, Akira Kanda, Seiji Shimono, Takaki Yun, Yasutaka Kobayashi, Yoshiki Wang, Zeyun Ooka, Hisashi Suzuki, Kensuke Van, Dan Bui Tomoda, Koichi Iwai, Hiroshi Nishiyama, Toshimasa Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia |
title | Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia |
title_full | Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia |
title_fullStr | Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia |
title_full_unstemmed | Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia |
title_short | Cells Expressing Prominin-1 in Neonatal Murine Inferior Colliculus Differentiate into Neurons and Glia |
title_sort | cells expressing prominin-1 in neonatal murine inferior colliculus differentiate into neurons and glia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5948249/ https://www.ncbi.nlm.nih.gov/pubmed/28795331 http://dx.doi.org/10.1007/s12035-017-0701-5 |
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