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X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis
Examination of histological or immunohistochemically stained 2D sections of embedded tissue is one of the most frequently used tools in biomedical research and clinical routine. Since to date, targeted sectioning of specific regions of interest (ROI) in the sample is not possible, we aimed at develo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955938/ https://www.ncbi.nlm.nih.gov/pubmed/29769600 http://dx.doi.org/10.1038/s41598-018-26086-0 |
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author | Albers, Jonas Markus, M. Andrea Alves, Frauke Dullin, Christian |
author_facet | Albers, Jonas Markus, M. Andrea Alves, Frauke Dullin, Christian |
author_sort | Albers, Jonas |
collection | PubMed |
description | Examination of histological or immunohistochemically stained 2D sections of embedded tissue is one of the most frequently used tools in biomedical research and clinical routine. Since to date, targeted sectioning of specific regions of interest (ROI) in the sample is not possible, we aimed at developing a guided sectioning approach based on x-ray 3D virtual histology for heavy ion stained murine lung samples. For this purpose, we increased the contrast to noise ratio of a standard benchtop microCT by 5–10-fold using free-propagation phase contrast imaging and thus substantially improved image quality. We then show that microCT 3D datasets deliver more precise anatomical information and quantification of the sample than traditional histological sections, which display deformations of the tissue. To quantify these deformations caused by sectioning we developed the “Displacement Index (DI)”, which combines block-matching with the calculation of the local mutual information. We show that the DI substantially decreases when a femtosecond laser microtome is used for sections as opposed to a traditional microtome. In conclusion, our microCT based virtual histology approach can be used as a supplement and a guidance tool for traditional histology, providing 3D measurement capabilities and offering the ability to perform sectioning directly at an ROI. |
format | Online Article Text |
id | pubmed-5955938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59559382018-05-21 X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis Albers, Jonas Markus, M. Andrea Alves, Frauke Dullin, Christian Sci Rep Article Examination of histological or immunohistochemically stained 2D sections of embedded tissue is one of the most frequently used tools in biomedical research and clinical routine. Since to date, targeted sectioning of specific regions of interest (ROI) in the sample is not possible, we aimed at developing a guided sectioning approach based on x-ray 3D virtual histology for heavy ion stained murine lung samples. For this purpose, we increased the contrast to noise ratio of a standard benchtop microCT by 5–10-fold using free-propagation phase contrast imaging and thus substantially improved image quality. We then show that microCT 3D datasets deliver more precise anatomical information and quantification of the sample than traditional histological sections, which display deformations of the tissue. To quantify these deformations caused by sectioning we developed the “Displacement Index (DI)”, which combines block-matching with the calculation of the local mutual information. We show that the DI substantially decreases when a femtosecond laser microtome is used for sections as opposed to a traditional microtome. In conclusion, our microCT based virtual histology approach can be used as a supplement and a guidance tool for traditional histology, providing 3D measurement capabilities and offering the ability to perform sectioning directly at an ROI. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955938/ /pubmed/29769600 http://dx.doi.org/10.1038/s41598-018-26086-0 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Albers, Jonas Markus, M. Andrea Alves, Frauke Dullin, Christian X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis |
title | X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis |
title_full | X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis |
title_fullStr | X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis |
title_full_unstemmed | X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis |
title_short | X-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis |
title_sort | x-ray based virtual histology allows guided sectioning of heavy ion stained murine lungs for histological analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955938/ https://www.ncbi.nlm.nih.gov/pubmed/29769600 http://dx.doi.org/10.1038/s41598-018-26086-0 |
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