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Unlocking the human inner ear for therapeutic intervention
The human inner ear contains minute three-dimensional neurosensory structures that are deeply embedded within the skull base, rendering them relatively inaccessible to regenerative therapies for hearing loss. Here we provide a detailed characterisation of the functional architecture of the space tha...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643346/ https://www.ncbi.nlm.nih.gov/pubmed/36347918 http://dx.doi.org/10.1038/s41598-022-22203-2 |
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author | Li, Hao Agrawal, Sumit Rohani, Seyed Alireza Zhu, Ning Cacciabue, Daniela I. Rivolta, Marcelo N. Hartley, Douglas E. H. Jiang, Dan Ladak, Hanif M. O’Donoghue, Gerard M. Rask-Andersen, Helge |
author_facet | Li, Hao Agrawal, Sumit Rohani, Seyed Alireza Zhu, Ning Cacciabue, Daniela I. Rivolta, Marcelo N. Hartley, Douglas E. H. Jiang, Dan Ladak, Hanif M. O’Donoghue, Gerard M. Rask-Andersen, Helge |
author_sort | Li, Hao |
collection | PubMed |
description | The human inner ear contains minute three-dimensional neurosensory structures that are deeply embedded within the skull base, rendering them relatively inaccessible to regenerative therapies for hearing loss. Here we provide a detailed characterisation of the functional architecture of the space that hosts the cell bodies of the auditory nerve to make them safely accessible for the first time for therapeutic intervention. We used synchrotron phase-contrast imaging which offers the required microscopic soft-tissue contrast definition while simultaneously displaying precise bony anatomic detail. Using volume-rendering software we constructed highly accurate 3-dimensional representations of the inner ear. The cell bodies are arranged in a bony helical canal that spirals from the base of the cochlea to its apex; the canal volume is 1.6 μL but with a diffusion potential of 15 μL. Modelling data from 10 temporal bones enabled definition of a safe trajectory for therapeutic access while preserving the cochlea’s internal architecture. We validated the approach through surgical simulation, anatomical dissection and micro-radiographic analysis. These findings will facilitate future clinical trials of novel therapeutic interventions to restore hearing. |
format | Online Article Text |
id | pubmed-9643346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96433462022-11-15 Unlocking the human inner ear for therapeutic intervention Li, Hao Agrawal, Sumit Rohani, Seyed Alireza Zhu, Ning Cacciabue, Daniela I. Rivolta, Marcelo N. Hartley, Douglas E. H. Jiang, Dan Ladak, Hanif M. O’Donoghue, Gerard M. Rask-Andersen, Helge Sci Rep Article The human inner ear contains minute three-dimensional neurosensory structures that are deeply embedded within the skull base, rendering them relatively inaccessible to regenerative therapies for hearing loss. Here we provide a detailed characterisation of the functional architecture of the space that hosts the cell bodies of the auditory nerve to make them safely accessible for the first time for therapeutic intervention. We used synchrotron phase-contrast imaging which offers the required microscopic soft-tissue contrast definition while simultaneously displaying precise bony anatomic detail. Using volume-rendering software we constructed highly accurate 3-dimensional representations of the inner ear. The cell bodies are arranged in a bony helical canal that spirals from the base of the cochlea to its apex; the canal volume is 1.6 μL but with a diffusion potential of 15 μL. Modelling data from 10 temporal bones enabled definition of a safe trajectory for therapeutic access while preserving the cochlea’s internal architecture. We validated the approach through surgical simulation, anatomical dissection and micro-radiographic analysis. These findings will facilitate future clinical trials of novel therapeutic interventions to restore hearing. Nature Publishing Group UK 2022-11-08 /pmc/articles/PMC9643346/ /pubmed/36347918 http://dx.doi.org/10.1038/s41598-022-22203-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Hao Agrawal, Sumit Rohani, Seyed Alireza Zhu, Ning Cacciabue, Daniela I. Rivolta, Marcelo N. Hartley, Douglas E. H. Jiang, Dan Ladak, Hanif M. O’Donoghue, Gerard M. Rask-Andersen, Helge Unlocking the human inner ear for therapeutic intervention |
title | Unlocking the human inner ear for therapeutic intervention |
title_full | Unlocking the human inner ear for therapeutic intervention |
title_fullStr | Unlocking the human inner ear for therapeutic intervention |
title_full_unstemmed | Unlocking the human inner ear for therapeutic intervention |
title_short | Unlocking the human inner ear for therapeutic intervention |
title_sort | unlocking the human inner ear for therapeutic intervention |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643346/ https://www.ncbi.nlm.nih.gov/pubmed/36347918 http://dx.doi.org/10.1038/s41598-022-22203-2 |
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