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Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology

Mitochondria are highly dynamic organelles that can exhibit a wide range of morphologies. Mitochondrial morphology can differ significantly across cell types, reflecting different physiological needs, but can also change rapidly in response to stress or the activation of signaling pathways. Understa...

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Autores principales: Rohani, Ali, Kashatus, Jennifer A., Sessions, Dane T., Sharmin, Salma, Kashatus, David F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642274/
https://www.ncbi.nlm.nih.gov/pubmed/33144635
http://dx.doi.org/10.1038/s41598-020-75899-5
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author Rohani, Ali
Kashatus, Jennifer A.
Sessions, Dane T.
Sharmin, Salma
Kashatus, David F.
author_facet Rohani, Ali
Kashatus, Jennifer A.
Sessions, Dane T.
Sharmin, Salma
Kashatus, David F.
author_sort Rohani, Ali
collection PubMed
description Mitochondria are highly dynamic organelles that can exhibit a wide range of morphologies. Mitochondrial morphology can differ significantly across cell types, reflecting different physiological needs, but can also change rapidly in response to stress or the activation of signaling pathways. Understanding both the cause and consequences of these morphological changes is critical to fully understanding how mitochondrial function contributes to both normal and pathological physiology. However, while robust and quantitative analysis of mitochondrial morphology has become increasingly accessible, there is a need for new tools to generate and analyze large data sets of mitochondrial images in high throughput. The generation of such datasets is critical to fully benefit from rapidly evolving methods in data science, such as neural networks, that have shown tremendous value in extracting novel biological insights and generating new hypotheses. Here we describe a set of three computational tools, Cell Catcher, Mito Catcher and MiA, that we have developed to extract extensive mitochondrial network data on a single-cell level from multi-cell fluorescence images. Cell Catcher automatically separates and isolates individual cells from multi-cell images; Mito Catcher uses the statistical distribution of pixel intensities across the mitochondrial network to detect and remove background noise from the cell and segment the mitochondrial network; MiA uses the binarized mitochondrial network to perform more than 100 mitochondria-level and cell-level morphometric measurements. To validate the utility of this set of tools, we generated a database of morphological features for 630 individual cells that encode 0, 1 or 2 alleles of the mitochondrial fission GTPase Drp1 and demonstrate that these mitochondrial data could be used to predict Drp1 genotype with 87% accuracy. Together, this suite of tools enables the high-throughput and automated collection of detailed and quantitative mitochondrial structural information at a single-cell level. Furthermore, the data generated with these tools, when combined with advanced data science approaches, can be used to generate novel biological insights.
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spelling pubmed-76422742020-11-06 Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology Rohani, Ali Kashatus, Jennifer A. Sessions, Dane T. Sharmin, Salma Kashatus, David F. Sci Rep Article Mitochondria are highly dynamic organelles that can exhibit a wide range of morphologies. Mitochondrial morphology can differ significantly across cell types, reflecting different physiological needs, but can also change rapidly in response to stress or the activation of signaling pathways. Understanding both the cause and consequences of these morphological changes is critical to fully understanding how mitochondrial function contributes to both normal and pathological physiology. However, while robust and quantitative analysis of mitochondrial morphology has become increasingly accessible, there is a need for new tools to generate and analyze large data sets of mitochondrial images in high throughput. The generation of such datasets is critical to fully benefit from rapidly evolving methods in data science, such as neural networks, that have shown tremendous value in extracting novel biological insights and generating new hypotheses. Here we describe a set of three computational tools, Cell Catcher, Mito Catcher and MiA, that we have developed to extract extensive mitochondrial network data on a single-cell level from multi-cell fluorescence images. Cell Catcher automatically separates and isolates individual cells from multi-cell images; Mito Catcher uses the statistical distribution of pixel intensities across the mitochondrial network to detect and remove background noise from the cell and segment the mitochondrial network; MiA uses the binarized mitochondrial network to perform more than 100 mitochondria-level and cell-level morphometric measurements. To validate the utility of this set of tools, we generated a database of morphological features for 630 individual cells that encode 0, 1 or 2 alleles of the mitochondrial fission GTPase Drp1 and demonstrate that these mitochondrial data could be used to predict Drp1 genotype with 87% accuracy. Together, this suite of tools enables the high-throughput and automated collection of detailed and quantitative mitochondrial structural information at a single-cell level. Furthermore, the data generated with these tools, when combined with advanced data science approaches, can be used to generate novel biological insights. Nature Publishing Group UK 2020-11-03 /pmc/articles/PMC7642274/ /pubmed/33144635 http://dx.doi.org/10.1038/s41598-020-75899-5 Text en © The Author(s) 2020 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
Rohani, Ali
Kashatus, Jennifer A.
Sessions, Dane T.
Sharmin, Salma
Kashatus, David F.
Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology
title Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology
title_full Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology
title_fullStr Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology
title_full_unstemmed Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology
title_short Mito Hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology
title_sort mito hacker: a set of tools to enable high-throughput analysis of mitochondrial network morphology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642274/
https://www.ncbi.nlm.nih.gov/pubmed/33144635
http://dx.doi.org/10.1038/s41598-020-75899-5
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