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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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