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Restoration of auditory evoked responses by human ES cell-derived otic progenitors
Deafness is a condition with a high prevalence worldwide, produced primarily by the loss of the sensory hair cells and their associated spiral ganglion neurons (SGNs). Of all the forms of deafness, auditory neuropathy is of a particular concern. This condition, defined primarily by damage to the SGN...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480718/ https://www.ncbi.nlm.nih.gov/pubmed/22972191 http://dx.doi.org/10.1038/nature11415 |
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author | Chen, Wei Jongkamonwiwat, Nopporn Abbas, Leila Eshtan, Sarah Jacob Johnson, Stuart L. Kuhn, Stephanie Milo, Marta Thurlow, Johanna K. Andrews, Peter W. Marcotti, Walter Moore, Harry D. Rivolta, Marcelo N. |
author_facet | Chen, Wei Jongkamonwiwat, Nopporn Abbas, Leila Eshtan, Sarah Jacob Johnson, Stuart L. Kuhn, Stephanie Milo, Marta Thurlow, Johanna K. Andrews, Peter W. Marcotti, Walter Moore, Harry D. Rivolta, Marcelo N. |
author_sort | Chen, Wei |
collection | PubMed |
description | Deafness is a condition with a high prevalence worldwide, produced primarily by the loss of the sensory hair cells and their associated spiral ganglion neurons (SGNs). Of all the forms of deafness, auditory neuropathy is of a particular concern. This condition, defined primarily by damage to the SGNs with relative preservation of the hair cells (1), is responsible for a substantial proportion of patients with hearing impairment (2). While the loss of hair cells can be circumvented partially by a cochlear implant, no routine treatment is available for sensory neuron loss since poor innervation limits the prospective performance of an implant (3). Using stem cells to recover the damaged sensory circuitry is a potential therapeutic strategy. Here, we present a protocol to induce differentiation from human embryonic stem cells (hESCs) using signals involved in the initial specification of the otic placode. We obtained two types of otic progenitors able to differentiate in vitro into hair cell-like cells and auditory neurons that display expected electrophysiological properties. Moreover, when transplanted into an auditory neuropathy model, otic neuroprogenitors engraft, differentiate and significantly improve auditory evoked response (ABR) thresholds. These results should stimulate further research into the development of a cell-based therapy for deafness. |
format | Online Article Text |
id | pubmed-3480718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-34807182013-04-11 Restoration of auditory evoked responses by human ES cell-derived otic progenitors Chen, Wei Jongkamonwiwat, Nopporn Abbas, Leila Eshtan, Sarah Jacob Johnson, Stuart L. Kuhn, Stephanie Milo, Marta Thurlow, Johanna K. Andrews, Peter W. Marcotti, Walter Moore, Harry D. Rivolta, Marcelo N. Nature Article Deafness is a condition with a high prevalence worldwide, produced primarily by the loss of the sensory hair cells and their associated spiral ganglion neurons (SGNs). Of all the forms of deafness, auditory neuropathy is of a particular concern. This condition, defined primarily by damage to the SGNs with relative preservation of the hair cells (1), is responsible for a substantial proportion of patients with hearing impairment (2). While the loss of hair cells can be circumvented partially by a cochlear implant, no routine treatment is available for sensory neuron loss since poor innervation limits the prospective performance of an implant (3). Using stem cells to recover the damaged sensory circuitry is a potential therapeutic strategy. Here, we present a protocol to induce differentiation from human embryonic stem cells (hESCs) using signals involved in the initial specification of the otic placode. We obtained two types of otic progenitors able to differentiate in vitro into hair cell-like cells and auditory neurons that display expected electrophysiological properties. Moreover, when transplanted into an auditory neuropathy model, otic neuroprogenitors engraft, differentiate and significantly improve auditory evoked response (ABR) thresholds. These results should stimulate further research into the development of a cell-based therapy for deafness. 2012-09-12 2012-10-11 /pmc/articles/PMC3480718/ /pubmed/22972191 http://dx.doi.org/10.1038/nature11415 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Chen, Wei Jongkamonwiwat, Nopporn Abbas, Leila Eshtan, Sarah Jacob Johnson, Stuart L. Kuhn, Stephanie Milo, Marta Thurlow, Johanna K. Andrews, Peter W. Marcotti, Walter Moore, Harry D. Rivolta, Marcelo N. Restoration of auditory evoked responses by human ES cell-derived otic progenitors |
title | Restoration of auditory evoked responses by human ES cell-derived otic progenitors |
title_full | Restoration of auditory evoked responses by human ES cell-derived otic progenitors |
title_fullStr | Restoration of auditory evoked responses by human ES cell-derived otic progenitors |
title_full_unstemmed | Restoration of auditory evoked responses by human ES cell-derived otic progenitors |
title_short | Restoration of auditory evoked responses by human ES cell-derived otic progenitors |
title_sort | restoration of auditory evoked responses by human es cell-derived otic progenitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480718/ https://www.ncbi.nlm.nih.gov/pubmed/22972191 http://dx.doi.org/10.1038/nature11415 |
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