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Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization

Current understanding of fibrosis remains incomplete despite the increasing burden of related diseases. Preclinical models are used to dissect the pathogenesis and dynamics of fibrosis, and to evaluate anti-fibrotic therapies. These studies require objective and accurate measurements of fibrosis. Ex...

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Autores principales: Courtoy, Guillaume E., Leclercq, Isabelle, Froidure, Antoine, Schiano, Guglielmo, Morelle, Johann, Devuyst, Olivier, Huaux, François, Bouzin, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709042/
https://www.ncbi.nlm.nih.gov/pubmed/33266431
http://dx.doi.org/10.3390/biom10111585
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author Courtoy, Guillaume E.
Leclercq, Isabelle
Froidure, Antoine
Schiano, Guglielmo
Morelle, Johann
Devuyst, Olivier
Huaux, François
Bouzin, Caroline
author_facet Courtoy, Guillaume E.
Leclercq, Isabelle
Froidure, Antoine
Schiano, Guglielmo
Morelle, Johann
Devuyst, Olivier
Huaux, François
Bouzin, Caroline
author_sort Courtoy, Guillaume E.
collection PubMed
description Current understanding of fibrosis remains incomplete despite the increasing burden of related diseases. Preclinical models are used to dissect the pathogenesis and dynamics of fibrosis, and to evaluate anti-fibrotic therapies. These studies require objective and accurate measurements of fibrosis. Existing histological quantification methods are operator-dependent, organ-specific, and/or need advanced equipment. Therefore, we developed a robust, minimally operator-dependent, and tissue-transposable digital method for fibrosis quantification. The proposed method involves a novel algorithm for more specific and more sensitive detection of collagen fibers stained by picrosirius red (PSR), a computer-assisted segmentation of histological structures, and a new automated morphological classification of fibers according to their compactness. The new algorithm proved more accurate than classical filtering using principal color component (red-green-blue; RGB) for PSR detection. We applied this new method on established mouse models of liver, lung, and kidney fibrosis and demonstrated its validity by evidencing topological collagen accumulation in relevant histological compartments. Our data also showed an overall accumulation of compact fibers concomitant with worsening fibrosis and evidenced topological changes in fiber compactness proper to each model. In conclusion, we describe here a robust digital method for fibrosis analysis allowing accurate quantification, pattern recognition, and multi-organ comparisons useful to understand fibrosis dynamics.
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spelling pubmed-77090422020-12-03 Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization Courtoy, Guillaume E. Leclercq, Isabelle Froidure, Antoine Schiano, Guglielmo Morelle, Johann Devuyst, Olivier Huaux, François Bouzin, Caroline Biomolecules Article Current understanding of fibrosis remains incomplete despite the increasing burden of related diseases. Preclinical models are used to dissect the pathogenesis and dynamics of fibrosis, and to evaluate anti-fibrotic therapies. These studies require objective and accurate measurements of fibrosis. Existing histological quantification methods are operator-dependent, organ-specific, and/or need advanced equipment. Therefore, we developed a robust, minimally operator-dependent, and tissue-transposable digital method for fibrosis quantification. The proposed method involves a novel algorithm for more specific and more sensitive detection of collagen fibers stained by picrosirius red (PSR), a computer-assisted segmentation of histological structures, and a new automated morphological classification of fibers according to their compactness. The new algorithm proved more accurate than classical filtering using principal color component (red-green-blue; RGB) for PSR detection. We applied this new method on established mouse models of liver, lung, and kidney fibrosis and demonstrated its validity by evidencing topological collagen accumulation in relevant histological compartments. Our data also showed an overall accumulation of compact fibers concomitant with worsening fibrosis and evidenced topological changes in fiber compactness proper to each model. In conclusion, we describe here a robust digital method for fibrosis analysis allowing accurate quantification, pattern recognition, and multi-organ comparisons useful to understand fibrosis dynamics. MDPI 2020-11-22 /pmc/articles/PMC7709042/ /pubmed/33266431 http://dx.doi.org/10.3390/biom10111585 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Courtoy, Guillaume E.
Leclercq, Isabelle
Froidure, Antoine
Schiano, Guglielmo
Morelle, Johann
Devuyst, Olivier
Huaux, François
Bouzin, Caroline
Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization
title Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization
title_full Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization
title_fullStr Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization
title_full_unstemmed Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization
title_short Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization
title_sort digital image analysis of picrosirius red staining: a robust method for multi-organ fibrosis quantification and characterization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709042/
https://www.ncbi.nlm.nih.gov/pubmed/33266431
http://dx.doi.org/10.3390/biom10111585
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