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Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells
Reprogramming of metabolic pathways determines cell functions and fate. In our work, we have used organelle-targeted ATP biosensors to evaluate cellular metabolic settings with high resolution in real time. Our data indicate that mitochondria dynamically supply ATP for glucose phosphorylation in a v...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456002/ https://www.ncbi.nlm.nih.gov/pubmed/30304688 http://dx.doi.org/10.1016/j.celrep.2018.09.027 |
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author | Depaoli, Maria R. Karsten, Felix Madreiter-Sokolowski, Corina T. Klec, Christiane Gottschalk, Benjamin Bischof, Helmut Eroglu, Emrah Waldeck-Weiermair, Markus Simmen, Thomas Graier, Wolfgang F. Malli, Roland |
author_facet | Depaoli, Maria R. Karsten, Felix Madreiter-Sokolowski, Corina T. Klec, Christiane Gottschalk, Benjamin Bischof, Helmut Eroglu, Emrah Waldeck-Weiermair, Markus Simmen, Thomas Graier, Wolfgang F. Malli, Roland |
author_sort | Depaoli, Maria R. |
collection | PubMed |
description | Reprogramming of metabolic pathways determines cell functions and fate. In our work, we have used organelle-targeted ATP biosensors to evaluate cellular metabolic settings with high resolution in real time. Our data indicate that mitochondria dynamically supply ATP for glucose phosphorylation in a variety of cancer cell types. This hexokinase-dependent process seems to be reversed upon the removal of glucose or other hexose sugars. Our data further verify that mitochondria in cancer cells have increased ATP consumption. Similar subcellular ATP fluxes occurred in young mouse embryonic fibroblasts (MEFs). However, pancreatic beta cells, senescent MEFs, and MEFs lacking mitofusin 2 displayed completely different mitochondrial ATP dynamics, indicative of increased oxidative phosphorylation. Our findings add perspective to the variability of the cellular bioenergetics and demonstrate that live cell imaging of mitochondrial ATP dynamics is a powerful tool to evaluate metabolic flexibility and heterogeneity at a single-cell level. |
format | Online Article Text |
id | pubmed-6456002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-64560022019-04-09 Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells Depaoli, Maria R. Karsten, Felix Madreiter-Sokolowski, Corina T. Klec, Christiane Gottschalk, Benjamin Bischof, Helmut Eroglu, Emrah Waldeck-Weiermair, Markus Simmen, Thomas Graier, Wolfgang F. Malli, Roland Cell Rep Article Reprogramming of metabolic pathways determines cell functions and fate. In our work, we have used organelle-targeted ATP biosensors to evaluate cellular metabolic settings with high resolution in real time. Our data indicate that mitochondria dynamically supply ATP for glucose phosphorylation in a variety of cancer cell types. This hexokinase-dependent process seems to be reversed upon the removal of glucose or other hexose sugars. Our data further verify that mitochondria in cancer cells have increased ATP consumption. Similar subcellular ATP fluxes occurred in young mouse embryonic fibroblasts (MEFs). However, pancreatic beta cells, senescent MEFs, and MEFs lacking mitofusin 2 displayed completely different mitochondrial ATP dynamics, indicative of increased oxidative phosphorylation. Our findings add perspective to the variability of the cellular bioenergetics and demonstrate that live cell imaging of mitochondrial ATP dynamics is a powerful tool to evaluate metabolic flexibility and heterogeneity at a single-cell level. 2018-10-09 /pmc/articles/PMC6456002/ /pubmed/30304688 http://dx.doi.org/10.1016/j.celrep.2018.09.027 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Depaoli, Maria R. Karsten, Felix Madreiter-Sokolowski, Corina T. Klec, Christiane Gottschalk, Benjamin Bischof, Helmut Eroglu, Emrah Waldeck-Weiermair, Markus Simmen, Thomas Graier, Wolfgang F. Malli, Roland Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells |
title | Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells |
title_full | Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells |
title_fullStr | Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells |
title_full_unstemmed | Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells |
title_short | Real-Time Imaging of Mitochondrial ATP Dynamics Reveals the Metabolic Setting of Single Cells |
title_sort | real-time imaging of mitochondrial atp dynamics reveals the metabolic setting of single cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456002/ https://www.ncbi.nlm.nih.gov/pubmed/30304688 http://dx.doi.org/10.1016/j.celrep.2018.09.027 |
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