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The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro

OBJECTIVES: Spiral ganglion neurons (SGNs) include potential endogenous progenitor populations for the regeneration of the peripheral auditory system. However, whether these populations are present in adult mice is largely unknown. We examined the presence and characteristics of SGN-neural stem cell...

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Autores principales: Moon, Byoung-San, Ammothumkandy, Aswathy, Zhang, Naibo, Peng, Lei, Ibrayeva, Albina, Bay, Maxwell, Pratap, Athira, Park, Hong Ju, Bonaguidi, Michael Anthony, Lu, Wange
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Otorhinolaryngology-Head and Neck Surgery 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222184/
https://www.ncbi.nlm.nih.gov/pubmed/30309200
http://dx.doi.org/10.21053/ceo.2018.00878
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author Moon, Byoung-San
Ammothumkandy, Aswathy
Zhang, Naibo
Peng, Lei
Ibrayeva, Albina
Bay, Maxwell
Pratap, Athira
Park, Hong Ju
Bonaguidi, Michael Anthony
Lu, Wange
author_facet Moon, Byoung-San
Ammothumkandy, Aswathy
Zhang, Naibo
Peng, Lei
Ibrayeva, Albina
Bay, Maxwell
Pratap, Athira
Park, Hong Ju
Bonaguidi, Michael Anthony
Lu, Wange
author_sort Moon, Byoung-San
collection PubMed
description OBJECTIVES: Spiral ganglion neurons (SGNs) include potential endogenous progenitor populations for the regeneration of the peripheral auditory system. However, whether these populations are present in adult mice is largely unknown. We examined the presence and characteristics of SGN-neural stem cells (NSCs) in mice as a function of age. METHODS: The expression of Nestin and Ki67 was examined in sequentially dissected cochlear modiolar tissues from mice of different ages (from postnatal day to 24 weeks) and the sphere-forming populations from the SGNs were isolated and differentiated into different cell types. RESULTS: There were significant decreases in Nestin and Ki67 double-positive mitotic progenitor cells in vivo with increasing mouse age. The SGNs formed spheres exhibiting self-renewing activity and multipotent capacity, which were seen in NSCs and were capable of differentiating into neuron and glial cell types. The SGN spheres derived from mice at an early age (postnatal day or 2 weeks) contained more mitotic stem cells than those from mice at a late age. CONCLUSION. Our findings showed the presence of self-renewing and proliferative subtypes of SGN-NSCs which might serve as a promising source for the regeneration of auditory neurons even in adult mice.
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spelling pubmed-62221842018-12-01 The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro Moon, Byoung-San Ammothumkandy, Aswathy Zhang, Naibo Peng, Lei Ibrayeva, Albina Bay, Maxwell Pratap, Athira Park, Hong Ju Bonaguidi, Michael Anthony Lu, Wange Clin Exp Otorhinolaryngol Original Article OBJECTIVES: Spiral ganglion neurons (SGNs) include potential endogenous progenitor populations for the regeneration of the peripheral auditory system. However, whether these populations are present in adult mice is largely unknown. We examined the presence and characteristics of SGN-neural stem cells (NSCs) in mice as a function of age. METHODS: The expression of Nestin and Ki67 was examined in sequentially dissected cochlear modiolar tissues from mice of different ages (from postnatal day to 24 weeks) and the sphere-forming populations from the SGNs were isolated and differentiated into different cell types. RESULTS: There were significant decreases in Nestin and Ki67 double-positive mitotic progenitor cells in vivo with increasing mouse age. The SGNs formed spheres exhibiting self-renewing activity and multipotent capacity, which were seen in NSCs and were capable of differentiating into neuron and glial cell types. The SGN spheres derived from mice at an early age (postnatal day or 2 weeks) contained more mitotic stem cells than those from mice at a late age. CONCLUSION. Our findings showed the presence of self-renewing and proliferative subtypes of SGN-NSCs which might serve as a promising source for the regeneration of auditory neurons even in adult mice. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2018-12 2018-10-13 /pmc/articles/PMC6222184/ /pubmed/30309200 http://dx.doi.org/10.21053/ceo.2018.00878 Text en Copyright © 2018 by Korean Society of Otorhinolaryngology-Head and Neck Surgery This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Moon, Byoung-San
Ammothumkandy, Aswathy
Zhang, Naibo
Peng, Lei
Ibrayeva, Albina
Bay, Maxwell
Pratap, Athira
Park, Hong Ju
Bonaguidi, Michael Anthony
Lu, Wange
The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro
title The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro
title_full The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro
title_fullStr The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro
title_full_unstemmed The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro
title_short The Presence of Neural Stem Cells and Changes in Stem Cell-Like Activity With Age in Mouse Spiral Ganglion Cells In Vivo and In Vitro
title_sort presence of neural stem cells and changes in stem cell-like activity with age in mouse spiral ganglion cells in vivo and in vitro
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222184/
https://www.ncbi.nlm.nih.gov/pubmed/30309200
http://dx.doi.org/10.21053/ceo.2018.00878
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