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Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy

A detailed vascular visualization and adequate quantification is essential for the proper assessment of novel angiomodulating strategies. Here, we introduce an ex vivo micro-computed tomography (microCT)-based imaging approach for the 3D visualization of the entire vasculature down to the capillary...

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Autores principales: Schaad, Laura, Hlushchuk, Ruslan, Barré, Sébastien, Gianni-Barrera, Roberto, Haberthür, David, Banfi, Andrea, Djonov, Valentin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294414/
https://www.ncbi.nlm.nih.gov/pubmed/28169309
http://dx.doi.org/10.1038/srep41842
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author Schaad, Laura
Hlushchuk, Ruslan
Barré, Sébastien
Gianni-Barrera, Roberto
Haberthür, David
Banfi, Andrea
Djonov, Valentin
author_facet Schaad, Laura
Hlushchuk, Ruslan
Barré, Sébastien
Gianni-Barrera, Roberto
Haberthür, David
Banfi, Andrea
Djonov, Valentin
author_sort Schaad, Laura
collection PubMed
description A detailed vascular visualization and adequate quantification is essential for the proper assessment of novel angiomodulating strategies. Here, we introduce an ex vivo micro-computed tomography (microCT)-based imaging approach for the 3D visualization of the entire vasculature down to the capillary level and rapid estimation of the vascular volume and vessel size distribution. After perfusion with μAngiofil(®), a novel polymerizing contrast agent, low- and high-resolution scans (voxel side length: 2.58–0.66 μm) of the entire vasculature were acquired. Based on the microCT data, sites of interest were defined and samples further processed for correlative morphology. The solidified, autofluorescent μAngiofil(®) remained in the vasculature and allowed co-registering of the histological sections with the corresponding microCT-stack. The perfusion efficiency of μAngiofil(®) was validated based on lectin-stained histological sections: 98 ± 0.5% of the blood vessels were μAngiofil(®)-positive, whereas 93 ± 2.6% were lectin-positive. By applying this approach we analyzed the angiogenesis induced by the cell-based delivery of a controlled VEGF dose. Vascular density increased by 426% mainly through the augmentation of medium-sized vessels (20–40 μm). The introduced correlative and quantitative imaging approach is highly reproducible and allows a detailed 3D characterization of the vasculature and muscle tissue. Combined with histology, a broad range of complementary structural information can be obtained.
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spelling pubmed-52944142017-02-10 Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy Schaad, Laura Hlushchuk, Ruslan Barré, Sébastien Gianni-Barrera, Roberto Haberthür, David Banfi, Andrea Djonov, Valentin Sci Rep Article A detailed vascular visualization and adequate quantification is essential for the proper assessment of novel angiomodulating strategies. Here, we introduce an ex vivo micro-computed tomography (microCT)-based imaging approach for the 3D visualization of the entire vasculature down to the capillary level and rapid estimation of the vascular volume and vessel size distribution. After perfusion with μAngiofil(®), a novel polymerizing contrast agent, low- and high-resolution scans (voxel side length: 2.58–0.66 μm) of the entire vasculature were acquired. Based on the microCT data, sites of interest were defined and samples further processed for correlative morphology. The solidified, autofluorescent μAngiofil(®) remained in the vasculature and allowed co-registering of the histological sections with the corresponding microCT-stack. The perfusion efficiency of μAngiofil(®) was validated based on lectin-stained histological sections: 98 ± 0.5% of the blood vessels were μAngiofil(®)-positive, whereas 93 ± 2.6% were lectin-positive. By applying this approach we analyzed the angiogenesis induced by the cell-based delivery of a controlled VEGF dose. Vascular density increased by 426% mainly through the augmentation of medium-sized vessels (20–40 μm). The introduced correlative and quantitative imaging approach is highly reproducible and allows a detailed 3D characterization of the vasculature and muscle tissue. Combined with histology, a broad range of complementary structural information can be obtained. Nature Publishing Group 2017-02-07 /pmc/articles/PMC5294414/ /pubmed/28169309 http://dx.doi.org/10.1038/srep41842 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Schaad, Laura
Hlushchuk, Ruslan
Barré, Sébastien
Gianni-Barrera, Roberto
Haberthür, David
Banfi, Andrea
Djonov, Valentin
Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy
title Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy
title_full Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy
title_fullStr Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy
title_full_unstemmed Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy
title_short Correlative Imaging of the Murine Hind Limb Vasculature and Muscle Tissue by MicroCT and Light Microscopy
title_sort correlative imaging of the murine hind limb vasculature and muscle tissue by microct and light microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294414/
https://www.ncbi.nlm.nih.gov/pubmed/28169309
http://dx.doi.org/10.1038/srep41842
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