Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron Microscopy

Elastic fibres constitute an important component of the extracellular matrix and currently are the subject of intensive study in order to elucidate their assembly, function and involvement in cell–matrix interactions and disease. However, few studies to date have investigated the 3D architecture of...

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Main Authors: Philip N. Lewis, Robert D. Young, R. B. Souza, Andrew J. Quantock, Keith M. Meek
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Methods and Protocols
Subjects:
Online Access:https://www.mdpi.com/2409-9279/4/3/56
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spelling doaj-3e8ff88faa0e47539154b02589a0d4db2021-09-26T00:47:32ZengMDPI AGMethods and Protocols2409-92792021-08-014565610.3390/mps4030056Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron MicroscopyPhilip N. Lewis0Robert D. Young1R. B. Souza2Andrew J. Quantock3Keith M. Meek4Structural Biophysics Research Group, School of Optometry & Vision Sciences, Cardiff University, Cardiff CF24 4HQ, UKStructural Biophysics Research Group, School of Optometry & Vision Sciences, Cardiff University, Cardiff CF24 4HQ, UKDepartment of Genetics and Evolutionary Biology, University of São Paulo, Rua de Matão 05508-090, BrazilStructural Biophysics Research Group, School of Optometry & Vision Sciences, Cardiff University, Cardiff CF24 4HQ, UKStructural Biophysics Research Group, School of Optometry & Vision Sciences, Cardiff University, Cardiff CF24 4HQ, UKElastic fibres constitute an important component of the extracellular matrix and currently are the subject of intensive study in order to elucidate their assembly, function and involvement in cell–matrix interactions and disease. However, few studies to date have investigated the 3D architecture of the elastic fibre system in bulk tissue. We describe a protocol for preparation of tissue samples, including primary fixation and backscatter electron contrast-enhancement steps, through dehydration into stable resin-embedded blocks for volume electron microscopy. The use of low molecular weight tannic acid and alcoholic lead staining are critical stages in this procedure. Block preparation by ultramicrotomy and evaporative metal coating prior to microscopical examination are also described. We present images acquired from serial block face scanning electron microscopy of cornea and aorta showing target structures clearly differentiated from cells and other matrix components. The processing method imparts high contrast to fibrillin-containing elastic fibres, thus facilitating their segmentation and rendering into 3D reconstructions by image analysis software from large serial image datasets.https://www.mdpi.com/2409-9279/4/3/56fibrillinelastic fibre3D ultrastructurevolume electron microscopyconnective tissue
collection DOAJ
language English
format Article
sources DOAJ
author Philip N. Lewis
Robert D. Young
R. B. Souza
Andrew J. Quantock
Keith M. Meek
spellingShingle Philip N. Lewis
Robert D. Young
R. B. Souza
Andrew J. Quantock
Keith M. Meek
Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron Microscopy
Methods and Protocols
fibrillin
elastic fibre
3D ultrastructure
volume electron microscopy
connective tissue
author_facet Philip N. Lewis
Robert D. Young
R. B. Souza
Andrew J. Quantock
Keith M. Meek
author_sort Philip N. Lewis
title Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron Microscopy
title_short Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron Microscopy
title_full Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron Microscopy
title_fullStr Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron Microscopy
title_full_unstemmed Contrast-Enhanced Tissue Processing of Fibrillin-Rich Elastic Fibres for 3D Visualization by Volume Scanning Electron Microscopy
title_sort contrast-enhanced tissue processing of fibrillin-rich elastic fibres for 3d visualization by volume scanning electron microscopy
publisher MDPI AG
series Methods and Protocols
issn 2409-9279
publishDate 2021-08-01
description Elastic fibres constitute an important component of the extracellular matrix and currently are the subject of intensive study in order to elucidate their assembly, function and involvement in cell–matrix interactions and disease. However, few studies to date have investigated the 3D architecture of the elastic fibre system in bulk tissue. We describe a protocol for preparation of tissue samples, including primary fixation and backscatter electron contrast-enhancement steps, through dehydration into stable resin-embedded blocks for volume electron microscopy. The use of low molecular weight tannic acid and alcoholic lead staining are critical stages in this procedure. Block preparation by ultramicrotomy and evaporative metal coating prior to microscopical examination are also described. We present images acquired from serial block face scanning electron microscopy of cornea and aorta showing target structures clearly differentiated from cells and other matrix components. The processing method imparts high contrast to fibrillin-containing elastic fibres, thus facilitating their segmentation and rendering into 3D reconstructions by image analysis software from large serial image datasets.
topic fibrillin
elastic fibre
3D ultrastructure
volume electron microscopy
connective tissue
url https://www.mdpi.com/2409-9279/4/3/56
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