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Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss

The peripheral auditory nerve (AN) carries sound information from sensory hair cells to the brain. The present study investigated the contribution of mouse and human hematopoietic stem cells (HSCs) to cellular diversity in the AN following the destruction of neuron cell bodies, also known as spiral...

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Autores principales: Lang, Hainan, Nishimoto, Eishi, Xing, Yazhi, Brown, LaShardai N, Noble, Kenyaria V, Barth, Jeremy L, LaRue, Amanda C, Ando, Kiyoshi, Schulte, Bradley A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154482/
https://www.ncbi.nlm.nih.gov/pubmed/27600399
http://dx.doi.org/10.1038/mt.2016.174
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author Lang, Hainan
Nishimoto, Eishi
Xing, Yazhi
Brown, LaShardai N
Noble, Kenyaria V
Barth, Jeremy L
LaRue, Amanda C
Ando, Kiyoshi
Schulte, Bradley A
author_facet Lang, Hainan
Nishimoto, Eishi
Xing, Yazhi
Brown, LaShardai N
Noble, Kenyaria V
Barth, Jeremy L
LaRue, Amanda C
Ando, Kiyoshi
Schulte, Bradley A
author_sort Lang, Hainan
collection PubMed
description The peripheral auditory nerve (AN) carries sound information from sensory hair cells to the brain. The present study investigated the contribution of mouse and human hematopoietic stem cells (HSCs) to cellular diversity in the AN following the destruction of neuron cell bodies, also known as spiral ganglion neurons (SGNs). Exposure of the adult mouse cochlea to ouabain selectively killed type I SGNs and disrupted the blood-labyrinth barrier. This procedure also resulted in the upregulation of genes associated with hematopoietic cell homing and differentiation, and provided an environment conducive to the tissue engraftment of circulating stem/progenitor cells into the AN. Experiments were performed using both a mouse-mouse bone marrow transplantation model and a severely immune-incompetent mouse model transplanted with human CD34(+) cord blood cells. Quantitative immunohistochemical analysis of recipient mice demonstrated that ouabain injury promoted an increase in the number of both HSC-derived macrophages and HSC-derived nonmacrophages in the AN. Although rare, a few HSC-derived cells in the injured AN exhibited glial-like qualities. These results suggest that human hematopoietic cells participate in remodeling of the AN after neuron cell body loss and that hematopoietic cells can be an important resource for promoting AN repair/regeneration in the adult inner ear.
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spelling pubmed-51544822016-12-26 Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss Lang, Hainan Nishimoto, Eishi Xing, Yazhi Brown, LaShardai N Noble, Kenyaria V Barth, Jeremy L LaRue, Amanda C Ando, Kiyoshi Schulte, Bradley A Mol Ther Original Article The peripheral auditory nerve (AN) carries sound information from sensory hair cells to the brain. The present study investigated the contribution of mouse and human hematopoietic stem cells (HSCs) to cellular diversity in the AN following the destruction of neuron cell bodies, also known as spiral ganglion neurons (SGNs). Exposure of the adult mouse cochlea to ouabain selectively killed type I SGNs and disrupted the blood-labyrinth barrier. This procedure also resulted in the upregulation of genes associated with hematopoietic cell homing and differentiation, and provided an environment conducive to the tissue engraftment of circulating stem/progenitor cells into the AN. Experiments were performed using both a mouse-mouse bone marrow transplantation model and a severely immune-incompetent mouse model transplanted with human CD34(+) cord blood cells. Quantitative immunohistochemical analysis of recipient mice demonstrated that ouabain injury promoted an increase in the number of both HSC-derived macrophages and HSC-derived nonmacrophages in the AN. Although rare, a few HSC-derived cells in the injured AN exhibited glial-like qualities. These results suggest that human hematopoietic cells participate in remodeling of the AN after neuron cell body loss and that hematopoietic cells can be an important resource for promoting AN repair/regeneration in the adult inner ear. Nature Publishing Group 2016-11 2016-10-04 /pmc/articles/PMC5154482/ /pubmed/27600399 http://dx.doi.org/10.1038/mt.2016.174 Text en Copyright © 2016 Official journal of the American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 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-nc-sa/4.0/
spellingShingle Original Article
Lang, Hainan
Nishimoto, Eishi
Xing, Yazhi
Brown, LaShardai N
Noble, Kenyaria V
Barth, Jeremy L
LaRue, Amanda C
Ando, Kiyoshi
Schulte, Bradley A
Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss
title Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss
title_full Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss
title_fullStr Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss
title_full_unstemmed Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss
title_short Contributions of Mouse and Human Hematopoietic Cells to Remodeling of the Adult Auditory Nerve After Neuron Loss
title_sort contributions of mouse and human hematopoietic cells to remodeling of the adult auditory nerve after neuron loss
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154482/
https://www.ncbi.nlm.nih.gov/pubmed/27600399
http://dx.doi.org/10.1038/mt.2016.174
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