5 results on '"Mayeuf-Louchart A"'
Search Results
2. MuscleJ2: a rebuilding of MuscleJ with new features for high-content analysis of skeletal muscle immunofluorescence slides
- Author
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Anne Danckaert, Aurélie Trignol, Guillaume Le Loher, Sébastien Loubens, Bart Staels, Hélène Duez, Spencer L. Shorte, and Alicia Mayeuf-Louchart
- Subjects
Histology ,Muscle fiber morphology ,Centro- and perinuclei ,Fiber typing ,Vascularization ,Phenotype cartography ,Diseases of the musculoskeletal system ,RC925-935 - Abstract
Abstract Histological analysis of skeletal muscle is of major interest for understanding its behavior in different pathophysiological conditions, such as the response to different environments or myopathies. In this context, many software programs have been developed to perform automated high-content analysis. We created MuscleJ, a macro that runs in ImageJ/Fiji on batches of images. MuscleJ is a multianalysis tool that initially allows the analysis of muscle fibers, capillaries, and satellite cells. Since its creation, it has been used in many studies, and we have further developed the software and added new features, which are presented in this article. We converted the macro into a Java-language plugin with an improved user interface. MuscleJ2 provides quantitative analysis of fibrosis, vascularization, and cell phenotype in whole muscle sections. It also performs analysis of the peri-myonuclei, the individual capillaries, and any staining in the muscle fibers, providing accurate quantification within regional sublocalizations of the fiber. A multicartography option allows users to visualize multiple results simultaneously. The plugin is freely available to the muscle science community.
- Published
- 2023
- Full Text
- View/download PDF
3. MuscleJ: a high-content analysis method to study skeletal muscle with a new Fiji tool
- Author
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Alicia Mayeuf-Louchart, David Hardy, Quentin Thorel, Pascal Roux, Lorna Gueniot, David Briand, Aurélien Mazeraud, Adrien Bouglé, Spencer L. Shorte, Bart Staels, Fabrice Chrétien, Hélène Duez, and Anne Danckaert
- Subjects
Skeletal muscle fiber ,Histology ,Image automated quantification ,In situ cartography ,Fiber typing ,Satellite cells ,Diseases of the musculoskeletal system ,RC925-935 - Abstract
Abstract Background Skeletal muscle has the capacity to adapt to environmental changes and regenerate upon injury. To study these processes, most experimental methods use quantification of parameters obtained from images of immunostained skeletal muscle. Muscle cross-sectional area, fiber typing, localization of nuclei within the muscle fiber, the number of vessels, and fiber-associated stem cells are used to assess muscle physiology. Manual quantification of these parameters is time consuming and only poorly reproducible. While current state-of-the-art software tools are unable to analyze all these parameters simultaneously, we have developed MuscleJ, a new bioinformatics tool to do so. Methods Running on the popular open source Fiji software platform, MuscleJ simultaneously analyzes parameters from immunofluorescent staining, imaged by different acquisition systems in a completely automated manner. Results After segmentation of muscle fibers, up to three other channels can be analyzed simultaneously. Dialog boxes make MuscleJ easy-to-use for biologists. In addition, we have implemented color in situ cartographies of results, allowing the user to directly visualize results on reconstituted muscle sections. Conclusion We report here that MuscleJ results were comparable to manual observations made by five experts. MuscleJ markedly enhances statistical analysis by allowing reliable comparison of skeletal muscle physiology-pathology results obtained from different laboratories using different acquisition systems. Providing fast robust multi-parameter analyses of skeletal muscle physiology-pathology, MuscleJ is available as a free tool for the skeletal muscle community.
- Published
- 2018
- Full Text
- View/download PDF
4. MuscleJ: a high-content analysis method to study skeletal muscle with a new Fiji tool
- Author
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Mayeuf-Louchart, Alicia, Hardy, David, Thorel, Quentin, Roux, Pascal, Gueniot, Lorna, Briand, David, Mazeraud, Aurélien, Bouglé, Adrien, Shorte, Spencer L., Staels, Bart, Chrétien, Fabrice, Duez, Hélène, and Danckaert, Anne
- Published
- 2018
- Full Text
- View/download PDF
5. MuscleJ: a high-content analysis method to study skeletal muscle with a new Fiji tool
- Author
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Hélène Duez, Adrien Bouglé, David Briand, Pascal Roux, Bart Staels, Lorna Guéniot, Anne Danckaert, Spencer L. Shorte, Alicia Mayeuf-Louchart, Quentin Thorel, Fabrice Chrétien, David Hardy, Aurélien Mazeraud, Récepteurs nucléaires, maladies cardiovasculaires et diabète - U 1011 (RNMCD), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Neuropathologie expérimentale - Experimental neuropathology, Institut Pasteur [Paris]-Université Paris Descartes - Paris 5 (UPD5), Institut Pasteur [Paris], BioImagerie Photonique – Photonic BioImaging (UTechS PBI), This work was supported by research grants from the Association Française contre les Myopathies AFM (to AML, FC and DH), Fédération Francophone de Recherche sur le Diabète FFRD, sponsored by Fédération Française des Diabétiques (AFD), AstraZeneca, Eli Lilly, Merck Sharp & Dohme (MSD), Novo Nordisk & Sanofi, (to HD), Fondation de France (to HD), the 'European Genomic Institute for Diabetes' (EGID, ANR-10-LABX-46) (to HD and BS), the Fondation des Gueules Cassées (DH and FC), and an ERC-Région Hauts de France funding (to HD). BS is a holder of an ERC advanced grant no. 694717 'Bile acid, immune-metabolism, lipid and glucose homeostasis'. The PBI (AD, PR, and SLS) is part of the France BioImaging infrastructure supported by the French National Research Agency (ANR-10-INSB-04-01, 'Investments for the future'), ANR-10-LABX-0046,EGID,EGID Diabetes Pole(2010), ANR-10-INBS-0004,France-BioImaging,Développment d'une infrastructure française distribuée coordonnée(2010), European Project: 694717,H2020-EU.1.1. - EXCELLENT SCIENCE - European Research Council (ERC) ,ImmunoBile(2016), Récepteurs nucléaires, maladies cardiovasculaires et diabète (EGID), Université de Lille, Droit et Santé-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Technologie et Service BioImagerie Photonique – Photonic BioImaging (UTechS PBI), Centre de Ressources et de Recherche Technologique - Center for Technological Resources and Research (C2RT), Institut Pasteur [Paris]-Institut Pasteur [Paris], ANR-10-LABX-0046/10-LABX-0046,EGID,EGID Diabetes Pole(2010), ANR-10-INBS-04-01/10-INBS-0004,France-BioImaging,Développment d'une infrastructure française distribuée coordonnée(2010), Institut Pasteur [Paris] (IP)-Université Paris Descartes - Paris 5 (UPD5), and Institut Pasteur [Paris] (IP)
- Subjects
0301 basic medicine ,lcsh:Diseases of the musculoskeletal system ,Histology ,Computer science ,Muscle Fibers, Skeletal ,Stem cells ,In situ cartography ,03 medical and health sciences ,Mice ,Software ,Satellite cells ,medicine ,Image Processing, Computer-Assisted ,[SDV.MHEP.AHA]Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO] ,Animals ,Orthopedics and Sports Medicine ,Segmentation ,Statistical analysis ,Muscle fibre ,Molecular Biology ,business.industry ,Optical Imaging ,Methodology ,Skeletal muscle ,Cell Biology ,Skeletal muscle fiber ,030104 developmental biology ,medicine.anatomical_structure ,Open source ,Fiber typing ,Image automated quantification ,Vessels ,Experimental methods ,lcsh:RC925-935 ,business ,Biomedical engineering ,Muscle physiology - Abstract
Background Skeletal muscle has the capacity to adapt to environmental changes and regenerate upon injury. To study these processes, most experimental methods use quantification of parameters obtained from images of immunostained skeletal muscle. Muscle cross-sectional area, fiber typing, localization of nuclei within the muscle fiber, the number of vessels, and fiber-associated stem cells are used to assess muscle physiology. Manual quantification of these parameters is time consuming and only poorly reproducible. While current state-of-the-art software tools are unable to analyze all these parameters simultaneously, we have developed MuscleJ, a new bioinformatics tool to do so. Methods Running on the popular open source Fiji software platform, MuscleJ simultaneously analyzes parameters from immunofluorescent staining, imaged by different acquisition systems in a completely automated manner. Results After segmentation of muscle fibers, up to three other channels can be analyzed simultaneously. Dialog boxes make MuscleJ easy-to-use for biologists. In addition, we have implemented color in situ cartographies of results, allowing the user to directly visualize results on reconstituted muscle sections. Conclusion We report here that MuscleJ results were comparable to manual observations made by five experts. MuscleJ markedly enhances statistical analysis by allowing reliable comparison of skeletal muscle physiology-pathology results obtained from different laboratories using different acquisition systems. Providing fast robust multi-parameter analyses of skeletal muscle physiology-pathology, MuscleJ is available as a free tool for the skeletal muscle community. Electronic supplementary material The online version of this article (10.1186/s13395-018-0171-0) contains supplementary material, which is available to authorized users.
- Published
- 2018
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