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

Research output: Contribution to journalArticleResearchpeer review

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

Research Organisations

External Research Organisations

  • Laser Zentrum Hannover e.V. (LZH)
  • Cluster of Excellence Hearing4all
  • Hannover Medical School (MHH)
  • Carl von Ossietzky University of Oldenburg
  • NIFE - Lower Saxony Centre for Biomedical Engineering, Implant Research and Development
View graph of relations

Details

Original languageEnglish
Article numbere0175431
JournalPLoS ONE
Volume12
Issue number4
Publication statusPublished - 7 Apr 2017

Abstract

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.

ASJC Scopus subject areas

Cite this

Scanning laser optical tomography for in toto imaging of the murine cochlea. / Nolte, Lena; Tinne, Nadine; Schulze, Jennifer et al.
In: PLoS ONE, Vol. 12, No. 4, e0175431, 07.04.2017.

Research output: Contribution to journalArticleResearchpeer review

Nolte, L, Tinne, N, Schulze, J, Heinemann, D, Antonopoulos, GC, Meyer, H, Nothwang, HG, Lenarz, T, Heisterkamp, A, Warnecke, A & Ripken, T 2017, 'Scanning laser optical tomography for in toto imaging of the murine cochlea', PLoS ONE, vol. 12, no. 4, e0175431. https://doi.org/10.1371/journal.pone.0175431
Nolte, L., Tinne, N., Schulze, J., Heinemann, D., Antonopoulos, G. C., Meyer, H., Nothwang, H. G., Lenarz, T., Heisterkamp, A., Warnecke, A., & Ripken, T. (2017). Scanning laser optical tomography for in toto imaging of the murine cochlea. PLoS ONE, 12(4), Article e0175431. https://doi.org/10.1371/journal.pone.0175431
Nolte L, Tinne N, Schulze J, Heinemann D, Antonopoulos GC, Meyer H et al. Scanning laser optical tomography for in toto imaging of the murine cochlea. PLoS ONE. 2017 Apr 7;12(4):e0175431. doi: 10.1371/journal.pone.0175431
Nolte, Lena ; Tinne, Nadine ; Schulze, Jennifer et al. / Scanning laser optical tomography for in toto imaging of the murine cochlea. In: PLoS ONE. 2017 ; Vol. 12, No. 4.
Download
@article{7e1b893e988e4828813ed2ab4a8448a3,
title = "Scanning laser optical tomography for in toto imaging of the murine cochlea",
abstract = "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.",
author = "Lena Nolte and Nadine Tinne and Jennifer Schulze and Dag Heinemann and Antonopoulos, {Georgios C.} and Heiko Meyer and Nothwang, {Hans Gerd} and Thomas Lenarz and Alexander Heisterkamp and Athanasia Warnecke and Tammo Ripken",
year = "2017",
month = apr,
day = "7",
doi = "10.1371/journal.pone.0175431",
language = "English",
volume = "12",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "4",

}

Download

TY - JOUR

T1 - Scanning laser optical tomography for in toto imaging of the murine cochlea

AU - Nolte, Lena

AU - Tinne, Nadine

AU - Schulze, Jennifer

AU - Heinemann, Dag

AU - Antonopoulos, Georgios C.

AU - Meyer, Heiko

AU - Nothwang, Hans Gerd

AU - Lenarz, Thomas

AU - Heisterkamp, Alexander

AU - Warnecke, Athanasia

AU - Ripken, Tammo

PY - 2017/4/7

Y1 - 2017/4/7

N2 - 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.

AB - 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.

UR - http://www.scopus.com/inward/record.url?scp=85017172616&partnerID=8YFLogxK

U2 - 10.1371/journal.pone.0175431

DO - 10.1371/journal.pone.0175431

M3 - Article

C2 - 28388662

AN - SCOPUS:85017172616

VL - 12

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 4

M1 - e0175431

ER -

By the same author(s)