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3D analysis of the myenteric plexus of the human bowel by X-ray phase-contrast tomography – a future method?
ISSN
0036-5521
Date Issued
2020
Author(s)
Peruzzi, Niccolò
Veress, Béla
Dahlin, Lars B.
Andersson, Mariam
Eckermann, Marina
Bech, Martin
Ohlsson, Bodil
DOI
10.1080/00365521.2020.1815079
Abstract
Objectives: Light microscopical analysis in two dimensions, combined with immunohistochemistry, is
presently the gold standard to describe the enteric nervous system (ENS). Our aim was to assess the
usefulness of three-dimensional (3D) imaging by X-ray phase-contrast tomography in evaluating the
ENS of the human bowel.
Material and methods: Myenteric ganglia were identified in full-thickness biopsies of the ileum and
colon by hematoxylin & eosin staining. A1-mm biopsy punch was taken from the paraffin blocks and
placed into a KaptonVR tube for subsequent tomographic investigation. The samples were scanned,
without further preparation, using phase-contrast tomography at two different scales: overview scans
(performed with laboratory setups), which allowed localization of the nervous tissue ( 1mm effective
voxel size); and high-resolution scans (performed with a synchrotron endstation), which imaged localized
regions of 320x320x320 mm3 (176 nm effective voxel size).
Results: The contrast allowed us to follow the shape and the size changes of the ganglia, as well as
to study their cellular components together with the cells and cellular projections of the periganglional
space. Furthermore, it was possible to show the 3D network of the myenteric plexus and to quantify
its volume within the samples.
Conclusions: Phase-contrast X-ray tomography can be applied for volume analyses of the human ENS
and to study tissue components in unstained paraffin-embedded tissue biopsies. This technique could
potentially be used to study disease mechanisms, and to compare healthy and diseased tissues in clinical
research.
presently the gold standard to describe the enteric nervous system (ENS). Our aim was to assess the
usefulness of three-dimensional (3D) imaging by X-ray phase-contrast tomography in evaluating the
ENS of the human bowel.
Material and methods: Myenteric ganglia were identified in full-thickness biopsies of the ileum and
colon by hematoxylin & eosin staining. A1-mm biopsy punch was taken from the paraffin blocks and
placed into a KaptonVR tube for subsequent tomographic investigation. The samples were scanned,
without further preparation, using phase-contrast tomography at two different scales: overview scans
(performed with laboratory setups), which allowed localization of the nervous tissue ( 1mm effective
voxel size); and high-resolution scans (performed with a synchrotron endstation), which imaged localized
regions of 320x320x320 mm3 (176 nm effective voxel size).
Results: The contrast allowed us to follow the shape and the size changes of the ganglia, as well as
to study their cellular components together with the cells and cellular projections of the periganglional
space. Furthermore, it was possible to show the 3D network of the myenteric plexus and to quantify
its volume within the samples.
Conclusions: Phase-contrast X-ray tomography can be applied for volume analyses of the human ENS
and to study tissue components in unstained paraffin-embedded tissue biopsies. This technique could
potentially be used to study disease mechanisms, and to compare healthy and diseased tissues in clinical
research.
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