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Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle

Skeletal muscle has the remarkable ability to regenerate. However, with age and disease muscle strength and function decline. Myofiber size, which is affected by injury and disease, is a critical measurement to assess muscle health. Here, we test and apply Cellpose, a recently developed deep learnin...

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Autores principales: Waisman, Ariel, Norris, Alessandra Marie, Elías Costa , Martín, Kopinke, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175575/
https://www.ncbi.nlm.nih.gov/pubmed/34083673
http://dx.doi.org/10.1038/s41598-021-91191-6
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author Waisman, Ariel
Norris, Alessandra Marie
Elías Costa , Martín
Kopinke, Daniel
author_facet Waisman, Ariel
Norris, Alessandra Marie
Elías Costa , Martín
Kopinke, Daniel
author_sort Waisman, Ariel
collection PubMed
description Skeletal muscle has the remarkable ability to regenerate. However, with age and disease muscle strength and function decline. Myofiber size, which is affected by injury and disease, is a critical measurement to assess muscle health. Here, we test and apply Cellpose, a recently developed deep learning algorithm, to automatically segment myofibers within murine skeletal muscle. We first show that tissue fixation is necessary to preserve cellular structures such as primary cilia, small cellular antennae, and adipocyte lipid droplets. However, fixation generates heterogeneous myofiber labeling, which impedes intensity-based segmentation. We demonstrate that Cellpose efficiently delineates thousands of individual myofibers outlined by a variety of markers, even within fixed tissue with highly uneven myofiber staining. We created a novel ImageJ plugin (LabelsToRois) that allows processing of multiple Cellpose segmentation images in batch. The plugin also contains a semi-automatic erosion function to correct for the area bias introduced by the different stainings, thereby identifying myofibers as accurately as human experts. We successfully applied our segmentation pipeline to uncover myofiber regeneration differences between two different muscle injury models, cardiotoxin and glycerol. Thus, Cellpose combined with LabelsToRois allows for fast, unbiased, and reproducible myofiber quantification for a variety of staining and fixation conditions.
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spelling pubmed-81755752021-06-07 Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle Waisman, Ariel Norris, Alessandra Marie Elías Costa , Martín Kopinke, Daniel Sci Rep Article Skeletal muscle has the remarkable ability to regenerate. However, with age and disease muscle strength and function decline. Myofiber size, which is affected by injury and disease, is a critical measurement to assess muscle health. Here, we test and apply Cellpose, a recently developed deep learning algorithm, to automatically segment myofibers within murine skeletal muscle. We first show that tissue fixation is necessary to preserve cellular structures such as primary cilia, small cellular antennae, and adipocyte lipid droplets. However, fixation generates heterogeneous myofiber labeling, which impedes intensity-based segmentation. We demonstrate that Cellpose efficiently delineates thousands of individual myofibers outlined by a variety of markers, even within fixed tissue with highly uneven myofiber staining. We created a novel ImageJ plugin (LabelsToRois) that allows processing of multiple Cellpose segmentation images in batch. The plugin also contains a semi-automatic erosion function to correct for the area bias introduced by the different stainings, thereby identifying myofibers as accurately as human experts. We successfully applied our segmentation pipeline to uncover myofiber regeneration differences between two different muscle injury models, cardiotoxin and glycerol. Thus, Cellpose combined with LabelsToRois allows for fast, unbiased, and reproducible myofiber quantification for a variety of staining and fixation conditions. Nature Publishing Group UK 2021-06-03 /pmc/articles/PMC8175575/ /pubmed/34083673 http://dx.doi.org/10.1038/s41598-021-91191-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Waisman, Ariel
Norris, Alessandra Marie
Elías Costa , Martín
Kopinke, Daniel
Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
title Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
title_full Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
title_fullStr Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
title_full_unstemmed Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
title_short Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
title_sort automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175575/
https://www.ncbi.nlm.nih.gov/pubmed/34083673
http://dx.doi.org/10.1038/s41598-021-91191-6
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