Scanning laser optical tomography for in toto imaging of the murine cochlea.

The mammalian cochlea is a complex macroscopic structure due to its helical shape and the microscopic arrangements of the individual layers of cells. To improve the outcomes of hearing restoration in deaf patients, it is important to understand the anatomic structure and composition of the cochlea e...

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Main Authors: Lena Nolte, Nadine Tinne, Jennifer Schulze, Dag Heinemann, Georgios C Antonopoulos, Heiko Meyer, Hans Gerd Nothwang, Thomas Lenarz, Alexander Heisterkamp, Athanasia Warnecke, Tammo Ripken
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5384786?pdf=render
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spelling doaj-06e9f2dce3574521b6859920167d4cf82020-11-25T01:46:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01124e017543110.1371/journal.pone.0175431Scanning laser optical tomography for in toto imaging of the murine cochlea.Lena NolteNadine TinneJennifer SchulzeDag HeinemannGeorgios C AntonopoulosHeiko MeyerHans Gerd NothwangThomas LenarzAlexander HeisterkampAthanasia WarneckeTammo RipkenThe mammalian cochlea is a complex macroscopic structure due to its helical shape and the microscopic arrangements of the individual layers of cells. To improve the outcomes of hearing restoration in deaf patients, it is important to understand the anatomic structure and composition of the cochlea ex vivo. Hitherto, only one histological technique based on confocal laser scanning microscopy and optical clearing has been developed for in toto optical imaging of the murine cochlea. However, with a growing size of the specimen, e.g., human cochlea, this technique reaches its limitations. Here, we demonstrate scanning laser optical tomography (SLOT) as a valuable imaging technique to visualize the murine cochlea in toto without any physical slicing. This technique can also be applied in larger specimens up to cm3 such as the human cochlea. Furthermore, immunolabeling allows visualization of inner hair cells (otoferlin) or spiral ganglion cells (neurofilament) within the whole cochlea. After image reconstruction, the 3D dataset was used for digital segmentation of the labeled region. As a result, quantitative analysis of position, length and curvature of the labeled region was possible. This is of high interest in order to understand the interaction of cochlear implants (CI) and cells in more detail.http://europepmc.org/articles/PMC5384786?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Lena Nolte
Nadine Tinne
Jennifer Schulze
Dag Heinemann
Georgios C Antonopoulos
Heiko Meyer
Hans Gerd Nothwang
Thomas Lenarz
Alexander Heisterkamp
Athanasia Warnecke
Tammo Ripken
spellingShingle Lena Nolte
Nadine Tinne
Jennifer Schulze
Dag Heinemann
Georgios C Antonopoulos
Heiko Meyer
Hans Gerd Nothwang
Thomas Lenarz
Alexander Heisterkamp
Athanasia Warnecke
Tammo Ripken
Scanning laser optical tomography for in toto imaging of the murine cochlea.
PLoS ONE
author_facet Lena Nolte
Nadine Tinne
Jennifer Schulze
Dag Heinemann
Georgios C Antonopoulos
Heiko Meyer
Hans Gerd Nothwang
Thomas Lenarz
Alexander Heisterkamp
Athanasia Warnecke
Tammo Ripken
author_sort Lena Nolte
title Scanning laser optical tomography for in toto imaging of the murine cochlea.
title_short Scanning laser optical tomography for in toto imaging of the murine cochlea.
title_full Scanning laser optical tomography for in toto imaging of the murine cochlea.
title_fullStr Scanning laser optical tomography for in toto imaging of the murine cochlea.
title_full_unstemmed Scanning laser optical tomography for in toto imaging of the murine cochlea.
title_sort scanning laser optical tomography for in toto imaging of the murine cochlea.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description The mammalian cochlea is a complex macroscopic structure due to its helical shape and the microscopic arrangements of the individual layers of cells. To improve the outcomes of hearing restoration in deaf patients, it is important to understand the anatomic structure and composition of the cochlea ex vivo. Hitherto, only one histological technique based on confocal laser scanning microscopy and optical clearing has been developed for in toto optical imaging of the murine cochlea. However, with a growing size of the specimen, e.g., human cochlea, this technique reaches its limitations. Here, we demonstrate scanning laser optical tomography (SLOT) as a valuable imaging technique to visualize the murine cochlea in toto without any physical slicing. This technique can also be applied in larger specimens up to cm3 such as the human cochlea. Furthermore, immunolabeling allows visualization of inner hair cells (otoferlin) or spiral ganglion cells (neurofilament) within the whole cochlea. After image reconstruction, the 3D dataset was used for digital segmentation of the labeled region. As a result, quantitative analysis of position, length and curvature of the labeled region was possible. This is of high interest in order to understand the interaction of cochlear implants (CI) and cells in more detail.
url http://europepmc.org/articles/PMC5384786?pdf=render
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