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High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions

Metabolic flux technology with the Seahorse bioanalyzer has emerged as a standard technique in cellular metabolism studies, allowing for simultaneous kinetic measurements of respiration and glycolysis. Methods to extend the utility and versatility of the metabolic flux assay would undoubtedly have i...

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Autores principales: Little, Andrew Charles, Kovalenko, Ilya, Goo, Laura Elaine, Hong, Hanna Sungok, Kerk, Samuel Andrew, Yates, Joel Anthony, Purohit, Vinee, Lombard, David Benner, Merajver, Sofia Diana, Lyssiotis, Costas Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260371/
https://www.ncbi.nlm.nih.gov/pubmed/32472013
http://dx.doi.org/10.1038/s42003-020-0988-z
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author Little, Andrew Charles
Kovalenko, Ilya
Goo, Laura Elaine
Hong, Hanna Sungok
Kerk, Samuel Andrew
Yates, Joel Anthony
Purohit, Vinee
Lombard, David Benner
Merajver, Sofia Diana
Lyssiotis, Costas Andreas
author_facet Little, Andrew Charles
Kovalenko, Ilya
Goo, Laura Elaine
Hong, Hanna Sungok
Kerk, Samuel Andrew
Yates, Joel Anthony
Purohit, Vinee
Lombard, David Benner
Merajver, Sofia Diana
Lyssiotis, Costas Andreas
author_sort Little, Andrew Charles
collection PubMed
description Metabolic flux technology with the Seahorse bioanalyzer has emerged as a standard technique in cellular metabolism studies, allowing for simultaneous kinetic measurements of respiration and glycolysis. Methods to extend the utility and versatility of the metabolic flux assay would undoubtedly have immediate and wide-reaching impacts. Herein, we describe a platform that couples the metabolic flux assay with high-content fluorescence imaging to simultaneously provide means for normalization of respiration data with cell number; analyze cell cycle distribution; and quantify mitochondrial content, fragmentation state, membrane potential, and mitochondrial reactive oxygen species. Integration of fluorescent dyes directly into the metabolic flux assay generates a more complete data set of mitochondrial features in a single assay. Moreover, application of this integrated strategy revealed insights into mitochondrial function following PGC1a and PRC1 inhibition in pancreatic cancer and demonstrated how the Rho-GTPases impact mitochondrial dynamics in breast cancer.
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spelling pubmed-72603712020-06-10 High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions Little, Andrew Charles Kovalenko, Ilya Goo, Laura Elaine Hong, Hanna Sungok Kerk, Samuel Andrew Yates, Joel Anthony Purohit, Vinee Lombard, David Benner Merajver, Sofia Diana Lyssiotis, Costas Andreas Commun Biol Article Metabolic flux technology with the Seahorse bioanalyzer has emerged as a standard technique in cellular metabolism studies, allowing for simultaneous kinetic measurements of respiration and glycolysis. Methods to extend the utility and versatility of the metabolic flux assay would undoubtedly have immediate and wide-reaching impacts. Herein, we describe a platform that couples the metabolic flux assay with high-content fluorescence imaging to simultaneously provide means for normalization of respiration data with cell number; analyze cell cycle distribution; and quantify mitochondrial content, fragmentation state, membrane potential, and mitochondrial reactive oxygen species. Integration of fluorescent dyes directly into the metabolic flux assay generates a more complete data set of mitochondrial features in a single assay. Moreover, application of this integrated strategy revealed insights into mitochondrial function following PGC1a and PRC1 inhibition in pancreatic cancer and demonstrated how the Rho-GTPases impact mitochondrial dynamics in breast cancer. Nature Publishing Group UK 2020-05-29 /pmc/articles/PMC7260371/ /pubmed/32472013 http://dx.doi.org/10.1038/s42003-020-0988-z 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Little, Andrew Charles
Kovalenko, Ilya
Goo, Laura Elaine
Hong, Hanna Sungok
Kerk, Samuel Andrew
Yates, Joel Anthony
Purohit, Vinee
Lombard, David Benner
Merajver, Sofia Diana
Lyssiotis, Costas Andreas
High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions
title High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions
title_full High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions
title_fullStr High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions
title_full_unstemmed High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions
title_short High-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions
title_sort high-content fluorescence imaging with the metabolic flux assay reveals insights into mitochondrial properties and functions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260371/
https://www.ncbi.nlm.nih.gov/pubmed/32472013
http://dx.doi.org/10.1038/s42003-020-0988-z
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