A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.

Structural abnormalities of the microvasculature can impair perfusion and function. Conventional histology provides good spatial resolution with which to evaluate the microvascular structure but affords no 3-dimensional information; this limitation could lead to misinterpretations of the complex mic...

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Main Authors: Yiwen Xu, J Geoffrey Pickering, Zengxuan Nong, Eli Gibson, John-Michael Arpino, Hao Yin, Aaron D Ward
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0126817
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spelling doaj-94734254737e4cc8bed9e7d8df5eb3b92021-03-03T20:03:37ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01105e012681710.1371/journal.pone.0126817A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.Yiwen XuJ Geoffrey PickeringZengxuan NongEli GibsonJohn-Michael ArpinoHao YinAaron D WardStructural abnormalities of the microvasculature can impair perfusion and function. Conventional histology provides good spatial resolution with which to evaluate the microvascular structure but affords no 3-dimensional information; this limitation could lead to misinterpretations of the complex microvessel network in health and disease. The objective of this study was to develop and evaluate an accurate, fully automated 3D histology reconstruction method to visualize the arterioles and venules within the mouse hind-limb. Sections of the tibialis anterior muscle from C57BL/J6 mice (both normal and subjected to femoral artery excision) were reconstructed using pairwise rigid and affine registrations of 5 µm-thick, paraffin-embedded serial sections digitized at 0.25 µm/pixel. Low-resolution intensity-based rigid registration was used to initialize the nucleus landmark-based registration, and conventional high-resolution intensity-based registration method. The affine nucleus landmark-based registration was developed in this work and was compared to the conventional affine high-resolution intensity-based registration method. Target registration errors were measured between adjacent tissue sections (pairwise error), as well as with respect to a 3D reference reconstruction (accumulated error, to capture propagation of error through the stack of sections). Accumulated error measures were lower (p < 0.01) for the nucleus landmark technique and superior vasculature continuity was observed. These findings indicate that registration based on automatic extraction and correspondence of small, homologous landmarks may support accurate 3D histology reconstruction. This technique avoids the otherwise problematic "banana-into-cylinder" effect observed using conventional methods that optimize the pairwise alignment of salient structures, forcing them to be section-orthogonal. This approach will provide a valuable tool for high-accuracy 3D histology tissue reconstructions for analysis of diseased microvasculature.https://doi.org/10.1371/journal.pone.0126817
collection DOAJ
language English
format Article
sources DOAJ
author Yiwen Xu
J Geoffrey Pickering
Zengxuan Nong
Eli Gibson
John-Michael Arpino
Hao Yin
Aaron D Ward
spellingShingle Yiwen Xu
J Geoffrey Pickering
Zengxuan Nong
Eli Gibson
John-Michael Arpino
Hao Yin
Aaron D Ward
A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.
PLoS ONE
author_facet Yiwen Xu
J Geoffrey Pickering
Zengxuan Nong
Eli Gibson
John-Michael Arpino
Hao Yin
Aaron D Ward
author_sort Yiwen Xu
title A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.
title_short A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.
title_full A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.
title_fullStr A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.
title_full_unstemmed A Method for 3D Histopathology Reconstruction Supporting Mouse Microvasculature Analysis.
title_sort method for 3d histopathology reconstruction supporting mouse microvasculature analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Structural abnormalities of the microvasculature can impair perfusion and function. Conventional histology provides good spatial resolution with which to evaluate the microvascular structure but affords no 3-dimensional information; this limitation could lead to misinterpretations of the complex microvessel network in health and disease. The objective of this study was to develop and evaluate an accurate, fully automated 3D histology reconstruction method to visualize the arterioles and venules within the mouse hind-limb. Sections of the tibialis anterior muscle from C57BL/J6 mice (both normal and subjected to femoral artery excision) were reconstructed using pairwise rigid and affine registrations of 5 µm-thick, paraffin-embedded serial sections digitized at 0.25 µm/pixel. Low-resolution intensity-based rigid registration was used to initialize the nucleus landmark-based registration, and conventional high-resolution intensity-based registration method. The affine nucleus landmark-based registration was developed in this work and was compared to the conventional affine high-resolution intensity-based registration method. Target registration errors were measured between adjacent tissue sections (pairwise error), as well as with respect to a 3D reference reconstruction (accumulated error, to capture propagation of error through the stack of sections). Accumulated error measures were lower (p < 0.01) for the nucleus landmark technique and superior vasculature continuity was observed. These findings indicate that registration based on automatic extraction and correspondence of small, homologous landmarks may support accurate 3D histology reconstruction. This technique avoids the otherwise problematic "banana-into-cylinder" effect observed using conventional methods that optimize the pairwise alignment of salient structures, forcing them to be section-orthogonal. This approach will provide a valuable tool for high-accuracy 3D histology tissue reconstructions for analysis of diseased microvasculature.
url https://doi.org/10.1371/journal.pone.0126817
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