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A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples

Development and study of cell-cultured constructs, such as tissue-engineering scaffolds or organ-on-a-chip platforms require a comprehensive, representative view on the cells inside the used materials. However, common characteristics of biomedical materials, for example, in porous, fibrous, rough-su...

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Autores principales: Tamminen, Ilmari, Lehto, Kalle, Hannula, Markus, Ojansivu, Miina, Johansson, Laura, Kellomäki, Minna, Miettinen, Susanna, Aula, Antti, Ihalainen, Teemu, Hyttinen, Jari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532209/
https://www.ncbi.nlm.nih.gov/pubmed/33009501
http://dx.doi.org/10.1038/s42003-020-01273-w
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author Tamminen, Ilmari
Lehto, Kalle
Hannula, Markus
Ojansivu, Miina
Johansson, Laura
Kellomäki, Minna
Miettinen, Susanna
Aula, Antti
Ihalainen, Teemu
Hyttinen, Jari
author_facet Tamminen, Ilmari
Lehto, Kalle
Hannula, Markus
Ojansivu, Miina
Johansson, Laura
Kellomäki, Minna
Miettinen, Susanna
Aula, Antti
Ihalainen, Teemu
Hyttinen, Jari
author_sort Tamminen, Ilmari
collection PubMed
description Development and study of cell-cultured constructs, such as tissue-engineering scaffolds or organ-on-a-chip platforms require a comprehensive, representative view on the cells inside the used materials. However, common characteristics of biomedical materials, for example, in porous, fibrous, rough-surfaced, and composite materials, can severely disturb low-energy imaging. In order to image and quantify cell structures in optically challenging samples, we combined labeling, 3D X-ray imaging, and in silico processing into a methodological pipeline. Cell-structure images were acquired by a tube-source X-ray microtomography device and compared to optical references for assessing the visual and quantitative accuracy. The spatial coverage of the X-ray imaging was demonstrated by investigating stem-cell nuclei inside clinically relevant-sized tissue-engineering scaffolds (5x13 mm) that were difficult to examine with the optical methods. Our results highlight the potential of the readily available X-ray microtomography devices that can be used to thoroughly study relative large cell-cultured samples with microscopic 3D accuracy.
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spelling pubmed-75322092020-10-19 A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples Tamminen, Ilmari Lehto, Kalle Hannula, Markus Ojansivu, Miina Johansson, Laura Kellomäki, Minna Miettinen, Susanna Aula, Antti Ihalainen, Teemu Hyttinen, Jari Commun Biol Article Development and study of cell-cultured constructs, such as tissue-engineering scaffolds or organ-on-a-chip platforms require a comprehensive, representative view on the cells inside the used materials. However, common characteristics of biomedical materials, for example, in porous, fibrous, rough-surfaced, and composite materials, can severely disturb low-energy imaging. In order to image and quantify cell structures in optically challenging samples, we combined labeling, 3D X-ray imaging, and in silico processing into a methodological pipeline. Cell-structure images were acquired by a tube-source X-ray microtomography device and compared to optical references for assessing the visual and quantitative accuracy. The spatial coverage of the X-ray imaging was demonstrated by investigating stem-cell nuclei inside clinically relevant-sized tissue-engineering scaffolds (5x13 mm) that were difficult to examine with the optical methods. Our results highlight the potential of the readily available X-ray microtomography devices that can be used to thoroughly study relative large cell-cultured samples with microscopic 3D accuracy. Nature Publishing Group UK 2020-10-02 /pmc/articles/PMC7532209/ /pubmed/33009501 http://dx.doi.org/10.1038/s42003-020-01273-w Text en © The Author(s) 2020 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
Tamminen, Ilmari
Lehto, Kalle
Hannula, Markus
Ojansivu, Miina
Johansson, Laura
Kellomäki, Minna
Miettinen, Susanna
Aula, Antti
Ihalainen, Teemu
Hyttinen, Jari
A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples
title A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples
title_full A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples
title_fullStr A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples
title_full_unstemmed A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples
title_short A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples
title_sort tube-source x-ray microtomography approach for quantitative 3d microscopy of optically challenging cell-cultured samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532209/
https://www.ncbi.nlm.nih.gov/pubmed/33009501
http://dx.doi.org/10.1038/s42003-020-01273-w
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