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Machine learning-based classification of mitochondrial morphology in primary neurons and brain
The mitochondrial network continually undergoes events of fission and fusion. Under physiologic conditions, the network is in equilibrium and is characterized by the presence of both elongated and punctate mitochondria. However, this balanced, homeostatic mitochondrial profile can change morphologic...
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/PMC7933342/ https://www.ncbi.nlm.nih.gov/pubmed/33664336 http://dx.doi.org/10.1038/s41598-021-84528-8 |
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author | Fogo, Garrett M. Anzell, Anthony R. Maheras, Kathleen J. Raghunayakula, Sarita Wider, Joseph M. Emaus, Katlynn J. Bryson, Timothy D. Bukowski, Melissa J. Neumar, Robert W. Przyklenk, Karin Sanderson, Thomas H. |
author_facet | Fogo, Garrett M. Anzell, Anthony R. Maheras, Kathleen J. Raghunayakula, Sarita Wider, Joseph M. Emaus, Katlynn J. Bryson, Timothy D. Bukowski, Melissa J. Neumar, Robert W. Przyklenk, Karin Sanderson, Thomas H. |
author_sort | Fogo, Garrett M. |
collection | PubMed |
description | The mitochondrial network continually undergoes events of fission and fusion. Under physiologic conditions, the network is in equilibrium and is characterized by the presence of both elongated and punctate mitochondria. However, this balanced, homeostatic mitochondrial profile can change morphologic distribution in response to various stressors. Therefore, it is imperative to develop a method that robustly measures mitochondrial morphology with high accuracy. Here, we developed a semi-automated image analysis pipeline for the quantitation of mitochondrial morphology for both in vitro and in vivo applications. The image analysis pipeline was generated and validated utilizing images of primary cortical neurons from transgenic mice, allowing genetic ablation of key components of mitochondrial dynamics. This analysis pipeline was further extended to evaluate mitochondrial morphology in vivo through immunolabeling of brain sections as well as serial block-face scanning electron microscopy. These data demonstrate a highly specific and sensitive method that accurately classifies distinct physiological and pathological mitochondrial morphologies. Furthermore, this workflow employs the use of readily available, free open-source software designed for high throughput image processing, segmentation, and analysis that is customizable to various biological models. |
format | Online Article Text |
id | pubmed-7933342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79333422021-03-08 Machine learning-based classification of mitochondrial morphology in primary neurons and brain Fogo, Garrett M. Anzell, Anthony R. Maheras, Kathleen J. Raghunayakula, Sarita Wider, Joseph M. Emaus, Katlynn J. Bryson, Timothy D. Bukowski, Melissa J. Neumar, Robert W. Przyklenk, Karin Sanderson, Thomas H. Sci Rep Article The mitochondrial network continually undergoes events of fission and fusion. Under physiologic conditions, the network is in equilibrium and is characterized by the presence of both elongated and punctate mitochondria. However, this balanced, homeostatic mitochondrial profile can change morphologic distribution in response to various stressors. Therefore, it is imperative to develop a method that robustly measures mitochondrial morphology with high accuracy. Here, we developed a semi-automated image analysis pipeline for the quantitation of mitochondrial morphology for both in vitro and in vivo applications. The image analysis pipeline was generated and validated utilizing images of primary cortical neurons from transgenic mice, allowing genetic ablation of key components of mitochondrial dynamics. This analysis pipeline was further extended to evaluate mitochondrial morphology in vivo through immunolabeling of brain sections as well as serial block-face scanning electron microscopy. These data demonstrate a highly specific and sensitive method that accurately classifies distinct physiological and pathological mitochondrial morphologies. Furthermore, this workflow employs the use of readily available, free open-source software designed for high throughput image processing, segmentation, and analysis that is customizable to various biological models. Nature Publishing Group UK 2021-03-04 /pmc/articles/PMC7933342/ /pubmed/33664336 http://dx.doi.org/10.1038/s41598-021-84528-8 Text en © The Author(s) 2021 Open Access This 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 Fogo, Garrett M. Anzell, Anthony R. Maheras, Kathleen J. Raghunayakula, Sarita Wider, Joseph M. Emaus, Katlynn J. Bryson, Timothy D. Bukowski, Melissa J. Neumar, Robert W. Przyklenk, Karin Sanderson, Thomas H. Machine learning-based classification of mitochondrial morphology in primary neurons and brain |
title | Machine learning-based classification of mitochondrial morphology in primary neurons and brain |
title_full | Machine learning-based classification of mitochondrial morphology in primary neurons and brain |
title_fullStr | Machine learning-based classification of mitochondrial morphology in primary neurons and brain |
title_full_unstemmed | Machine learning-based classification of mitochondrial morphology in primary neurons and brain |
title_short | Machine learning-based classification of mitochondrial morphology in primary neurons and brain |
title_sort | machine learning-based classification of mitochondrial morphology in primary neurons and brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933342/ https://www.ncbi.nlm.nih.gov/pubmed/33664336 http://dx.doi.org/10.1038/s41598-021-84528-8 |
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