Cargando…

Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies

Significance: Currently, tissue biopsies are sectioned into 3- to [Formula: see text]-thick slices that are used for conventional pathology analysis. Previous work by confocal microscopy and light-sheet microscopy has shown that analyzing biopsies intact in three-dimensions (3D) is possible and may...

Descripción completa

Detalles Bibliográficos
Autores principales: Boamfa, Marius I., Asselman, Michel J. A., Vulders, Roland C. M., Verhoef, Esther I., van Royen, Martin E., van der Zaag, Pieter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676494/
https://www.ncbi.nlm.nih.gov/pubmed/33215476
http://dx.doi.org/10.1117/1.JBO.25.11.116503
_version_ 1783611782031474688
author Boamfa, Marius I.
Asselman, Michel J. A.
Vulders, Roland C. M.
Verhoef, Esther I.
van Royen, Martin E.
van der Zaag, Pieter J.
author_facet Boamfa, Marius I.
Asselman, Michel J. A.
Vulders, Roland C. M.
Verhoef, Esther I.
van Royen, Martin E.
van der Zaag, Pieter J.
author_sort Boamfa, Marius I.
collection PubMed
description Significance: Currently, tissue biopsies are sectioned into 3- to [Formula: see text]-thick slices that are used for conventional pathology analysis. Previous work by confocal microscopy and light-sheet microscopy has shown that analyzing biopsies intact in three-dimensions (3D) is possible and may lead to a better understanding of cancer growth patterns. Although accurate, these methods require fluorescent staining of the tissue, in addition to tissue clearing. If the 3D biopsy analysis could be done sufficiently swiftly, this approach may be used for on-site assessment of the adequacy of a biopsy taken. Aim: We aim to show that, by transmission microscopy of optically cleared tissue punches, the tissue architecture can be determined without the need for fluorescent staining. Approach: Transmission microscopy is used by combining bright field microscopy with dark field and epifluorescent microscopy to compare samples that have also been analyzed by fluorescent confocal microscopy. Results: With increasing distance to the focal plane, the higher-frequency part of the spatial frequency spectrum of transmitted light is attenuated increasingly. This property is exploited for tissue segmentation, detecting whether tissue is present at a certain position in the focal plane image. Using this approach, we show that a 3D rendering of the internal cavity or tubules structure of punch biopsies, which are up to 1-mm thick, can be acquired in [Formula: see text] scan time per imaging modality. The images of the overall tissue architecture that are obtained are similar to those from the confocal microscopy benchmark, without requiring fluorescent staining. Conclusions: Images of the overall tissue architecture can be obtained from transmission microcopy; they are similar to those from the confocal microscopy benchmark without requiring fluorescent staining. Tissue clearing is still needed. The total scan time of the present method is significantly shorter at a fraction of the device costs.
format Online
Article
Text
id pubmed-7676494
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Society of Photo-Optical Instrumentation Engineers
record_format MEDLINE/PubMed
spelling pubmed-76764942020-11-25 Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies Boamfa, Marius I. Asselman, Michel J. A. Vulders, Roland C. M. Verhoef, Esther I. van Royen, Martin E. van der Zaag, Pieter J. J Biomed Opt Microscopy Significance: Currently, tissue biopsies are sectioned into 3- to [Formula: see text]-thick slices that are used for conventional pathology analysis. Previous work by confocal microscopy and light-sheet microscopy has shown that analyzing biopsies intact in three-dimensions (3D) is possible and may lead to a better understanding of cancer growth patterns. Although accurate, these methods require fluorescent staining of the tissue, in addition to tissue clearing. If the 3D biopsy analysis could be done sufficiently swiftly, this approach may be used for on-site assessment of the adequacy of a biopsy taken. Aim: We aim to show that, by transmission microscopy of optically cleared tissue punches, the tissue architecture can be determined without the need for fluorescent staining. Approach: Transmission microscopy is used by combining bright field microscopy with dark field and epifluorescent microscopy to compare samples that have also been analyzed by fluorescent confocal microscopy. Results: With increasing distance to the focal plane, the higher-frequency part of the spatial frequency spectrum of transmitted light is attenuated increasingly. This property is exploited for tissue segmentation, detecting whether tissue is present at a certain position in the focal plane image. Using this approach, we show that a 3D rendering of the internal cavity or tubules structure of punch biopsies, which are up to 1-mm thick, can be acquired in [Formula: see text] scan time per imaging modality. The images of the overall tissue architecture that are obtained are similar to those from the confocal microscopy benchmark, without requiring fluorescent staining. Conclusions: Images of the overall tissue architecture can be obtained from transmission microcopy; they are similar to those from the confocal microscopy benchmark without requiring fluorescent staining. Tissue clearing is still needed. The total scan time of the present method is significantly shorter at a fraction of the device costs. Society of Photo-Optical Instrumentation Engineers 2020-11-19 2020-11 /pmc/articles/PMC7676494/ /pubmed/33215476 http://dx.doi.org/10.1117/1.JBO.25.11.116503 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/ Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle Microscopy
Boamfa, Marius I.
Asselman, Michel J. A.
Vulders, Roland C. M.
Verhoef, Esther I.
van Royen, Martin E.
van der Zaag, Pieter J.
Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies
title Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies
title_full Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies
title_fullStr Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies
title_full_unstemmed Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies
title_short Combined transmission, dark field and fluorescence microscopy for intact, 3D tissue analysis of biopsies
title_sort combined transmission, dark field and fluorescence microscopy for intact, 3d tissue analysis of biopsies
topic Microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676494/
https://www.ncbi.nlm.nih.gov/pubmed/33215476
http://dx.doi.org/10.1117/1.JBO.25.11.116503
work_keys_str_mv AT boamfamariusi combinedtransmissiondarkfieldandfluorescencemicroscopyforintact3dtissueanalysisofbiopsies
AT asselmanmichelja combinedtransmissiondarkfieldandfluorescencemicroscopyforintact3dtissueanalysisofbiopsies
AT vuldersrolandcm combinedtransmissiondarkfieldandfluorescencemicroscopyforintact3dtissueanalysisofbiopsies
AT verhoefestheri combinedtransmissiondarkfieldandfluorescencemicroscopyforintact3dtissueanalysisofbiopsies
AT vanroyenmartine combinedtransmissiondarkfieldandfluorescencemicroscopyforintact3dtissueanalysisofbiopsies
AT vanderzaagpieterj combinedtransmissiondarkfieldandfluorescencemicroscopyforintact3dtissueanalysisofbiopsies