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3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography

A multiscale three-dimensional (3D) virtual histology approach is presented, based on two configurations of propagation phase-contrast X-ray tomography, which have been implemented in close proximity at the GINIX endstation at the beamline P10/PETRA III (DESY, Hamburg, Germany). This enables the 3D...

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Autores principales: Frohn, Jasper, Pinkert-Leetsch, Diana, Missbach-Güntner, Jeannine, Reichardt, Marius, Osterhoff, Markus, Alves, Frauke, Salditt, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642968/
https://www.ncbi.nlm.nih.gov/pubmed/33147198
http://dx.doi.org/10.1107/S1600577520011327
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author Frohn, Jasper
Pinkert-Leetsch, Diana
Missbach-Güntner, Jeannine
Reichardt, Marius
Osterhoff, Markus
Alves, Frauke
Salditt, Tim
author_facet Frohn, Jasper
Pinkert-Leetsch, Diana
Missbach-Güntner, Jeannine
Reichardt, Marius
Osterhoff, Markus
Alves, Frauke
Salditt, Tim
author_sort Frohn, Jasper
collection PubMed
description A multiscale three-dimensional (3D) virtual histology approach is presented, based on two configurations of propagation phase-contrast X-ray tomography, which have been implemented in close proximity at the GINIX endstation at the beamline P10/PETRA III (DESY, Hamburg, Germany). This enables the 3D reconstruction of characteristic morphological features of human pancreatic normal and tumor tissue, as obtained from cancer surgery, first in the form of a large-scale overview by parallel-beam illumination, followed by a zoom into a region-of-interest based on zoom tomography using a Kirkpatrick–Baez mirror with additional waveguide optics. To this end 1 mm punch biopsies of the tissue were taken. In the parallel tomography, a volumetric throughput on the order of 0.01 mm(3) s(−1) was achieved, while maintaining the ability to segment isolated cells. With a continuous rotation during the scan, a total acquisition time of less than 2 min was required for a full tomographic scan. Using the combination of both setups, islets of Langerhans, a three-dimensional cluster of cells in the endocrine part of the pancreas, could be located. Cells in such an islet were segmented and visualized in 3D. Further, morphological alterations of tumorous tissue of the pancreas were characterized. To this end, the anisotropy parameter Ω, based on intensity gradients, was used in order to quantify the presence of collagen fibers within the entire biopsy specimen. This proof-of-concept experiment of the multiscale approach on human pancreatic tissue paves the way for future 3D virtual pathology.
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spelling pubmed-76429682020-11-17 3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography Frohn, Jasper Pinkert-Leetsch, Diana Missbach-Güntner, Jeannine Reichardt, Marius Osterhoff, Markus Alves, Frauke Salditt, Tim J Synchrotron Radiat Research Papers A multiscale three-dimensional (3D) virtual histology approach is presented, based on two configurations of propagation phase-contrast X-ray tomography, which have been implemented in close proximity at the GINIX endstation at the beamline P10/PETRA III (DESY, Hamburg, Germany). This enables the 3D reconstruction of characteristic morphological features of human pancreatic normal and tumor tissue, as obtained from cancer surgery, first in the form of a large-scale overview by parallel-beam illumination, followed by a zoom into a region-of-interest based on zoom tomography using a Kirkpatrick–Baez mirror with additional waveguide optics. To this end 1 mm punch biopsies of the tissue were taken. In the parallel tomography, a volumetric throughput on the order of 0.01 mm(3) s(−1) was achieved, while maintaining the ability to segment isolated cells. With a continuous rotation during the scan, a total acquisition time of less than 2 min was required for a full tomographic scan. Using the combination of both setups, islets of Langerhans, a three-dimensional cluster of cells in the endocrine part of the pancreas, could be located. Cells in such an islet were segmented and visualized in 3D. Further, morphological alterations of tumorous tissue of the pancreas were characterized. To this end, the anisotropy parameter Ω, based on intensity gradients, was used in order to quantify the presence of collagen fibers within the entire biopsy specimen. This proof-of-concept experiment of the multiscale approach on human pancreatic tissue paves the way for future 3D virtual pathology. International Union of Crystallography 2020-10-23 /pmc/articles/PMC7642968/ /pubmed/33147198 http://dx.doi.org/10.1107/S1600577520011327 Text en © Jasper Frohn et al. 2020 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Papers
Frohn, Jasper
Pinkert-Leetsch, Diana
Missbach-Güntner, Jeannine
Reichardt, Marius
Osterhoff, Markus
Alves, Frauke
Salditt, Tim
3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography
title 3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography
title_full 3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography
title_fullStr 3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography
title_full_unstemmed 3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography
title_short 3D virtual histology of human pancreatic tissue by multiscale phase-contrast X-ray tomography
title_sort 3d virtual histology of human pancreatic tissue by multiscale phase-contrast x-ray tomography
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642968/
https://www.ncbi.nlm.nih.gov/pubmed/33147198
http://dx.doi.org/10.1107/S1600577520011327
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