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A novel retinal ganglion cell quantification tool based on deep learning
Glaucoma is a disease associated with the loss of retinal ganglion cells (RGCs), and remains one of the primary causes of blindness worldwide. Major research efforts are presently directed towards the understanding of disease pathogenesis and the development of new therapies, with the help of rodent...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804414/ https://www.ncbi.nlm.nih.gov/pubmed/33436866 http://dx.doi.org/10.1038/s41598-020-80308-y |
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author | Masin, Luca Claes, Marie Bergmans, Steven Cools, Lien Andries, Lien Davis, Benjamin M. Moons, Lieve De Groef, Lies |
author_facet | Masin, Luca Claes, Marie Bergmans, Steven Cools, Lien Andries, Lien Davis, Benjamin M. Moons, Lieve De Groef, Lies |
author_sort | Masin, Luca |
collection | PubMed |
description | Glaucoma is a disease associated with the loss of retinal ganglion cells (RGCs), and remains one of the primary causes of blindness worldwide. Major research efforts are presently directed towards the understanding of disease pathogenesis and the development of new therapies, with the help of rodent models as an important preclinical research tool. The ultimate goal is reaching neuroprotection of the RGCs, which requires a tool to reliably quantify RGC survival. Hence, we demonstrate a novel deep learning pipeline that enables fully automated RGC quantification in the entire murine retina. This software, called RGCode (Retinal Ganglion Cell quantification based On DEep learning), provides a user-friendly interface that requires the input of RBPMS-immunostained flatmounts and returns the total RGC count, retinal area and density, together with output images showing the computed counts and isodensity maps. The counting model was trained on RBPMS-stained healthy and glaucomatous retinas, obtained from mice subjected to microbead-induced ocular hypertension and optic nerve crush injury paradigms. RGCode demonstrates excellent performance in RGC quantification as compared to manual counts. Furthermore, we convincingly show that RGCode has potential for wider application, by retraining the model with a minimal set of training data to count FluoroGold-traced RGCs. |
format | Online Article Text |
id | pubmed-7804414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78044142021-01-13 A novel retinal ganglion cell quantification tool based on deep learning Masin, Luca Claes, Marie Bergmans, Steven Cools, Lien Andries, Lien Davis, Benjamin M. Moons, Lieve De Groef, Lies Sci Rep Article Glaucoma is a disease associated with the loss of retinal ganglion cells (RGCs), and remains one of the primary causes of blindness worldwide. Major research efforts are presently directed towards the understanding of disease pathogenesis and the development of new therapies, with the help of rodent models as an important preclinical research tool. The ultimate goal is reaching neuroprotection of the RGCs, which requires a tool to reliably quantify RGC survival. Hence, we demonstrate a novel deep learning pipeline that enables fully automated RGC quantification in the entire murine retina. This software, called RGCode (Retinal Ganglion Cell quantification based On DEep learning), provides a user-friendly interface that requires the input of RBPMS-immunostained flatmounts and returns the total RGC count, retinal area and density, together with output images showing the computed counts and isodensity maps. The counting model was trained on RBPMS-stained healthy and glaucomatous retinas, obtained from mice subjected to microbead-induced ocular hypertension and optic nerve crush injury paradigms. RGCode demonstrates excellent performance in RGC quantification as compared to manual counts. Furthermore, we convincingly show that RGCode has potential for wider application, by retraining the model with a minimal set of training data to count FluoroGold-traced RGCs. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804414/ /pubmed/33436866 http://dx.doi.org/10.1038/s41598-020-80308-y Text en © The Author(s) 2021 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/. |
spellingShingle | Article Masin, Luca Claes, Marie Bergmans, Steven Cools, Lien Andries, Lien Davis, Benjamin M. Moons, Lieve De Groef, Lies A novel retinal ganglion cell quantification tool based on deep learning |
title | A novel retinal ganglion cell quantification tool based on deep learning |
title_full | A novel retinal ganglion cell quantification tool based on deep learning |
title_fullStr | A novel retinal ganglion cell quantification tool based on deep learning |
title_full_unstemmed | A novel retinal ganglion cell quantification tool based on deep learning |
title_short | A novel retinal ganglion cell quantification tool based on deep learning |
title_sort | novel retinal ganglion cell quantification tool based on deep learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804414/ https://www.ncbi.nlm.nih.gov/pubmed/33436866 http://dx.doi.org/10.1038/s41598-020-80308-y |
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