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Monitoring ATP dynamics in electrically active white matter tracts
In several neurodegenerative diseases and myelin disorders, the degeneration profiles of myelinated axons are compatible with underlying energy deficits. However, it is presently impossible to measure selectively axonal ATP levels in the electrically active nervous system. We combined transgenic exp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415357/ https://www.ncbi.nlm.nih.gov/pubmed/28414271 http://dx.doi.org/10.7554/eLife.24241 |
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author | Trevisiol, Andrea Saab, Aiman S Winkler, Ulrike Marx, Grit Imamura, Hiromi Möbius, Wiebke Kusch, Kathrin Nave, Klaus-Armin Hirrlinger, Johannes |
author_facet | Trevisiol, Andrea Saab, Aiman S Winkler, Ulrike Marx, Grit Imamura, Hiromi Möbius, Wiebke Kusch, Kathrin Nave, Klaus-Armin Hirrlinger, Johannes |
author_sort | Trevisiol, Andrea |
collection | PubMed |
description | In several neurodegenerative diseases and myelin disorders, the degeneration profiles of myelinated axons are compatible with underlying energy deficits. However, it is presently impossible to measure selectively axonal ATP levels in the electrically active nervous system. We combined transgenic expression of an ATP-sensor in neurons of mice with confocal FRET imaging and electrophysiological recordings of acutely isolated optic nerves. This allowed us to monitor dynamic changes and activity-dependent axonal ATP homeostasis at the cellular level and in real time. We find that changes in ATP levels correlate well with compound action potentials. However, this correlation is disrupted when metabolism of lactate is inhibited, suggesting that axonal glycolysis products are not sufficient to maintain mitochondrial energy metabolism of electrically active axons. The combined monitoring of cellular ATP and electrical activity is a novel tool to study neuronal and glial energy metabolism in normal physiology and in models of neurodegenerative disorders. DOI: http://dx.doi.org/10.7554/eLife.24241.001 |
format | Online Article Text |
id | pubmed-5415357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54153572017-05-04 Monitoring ATP dynamics in electrically active white matter tracts Trevisiol, Andrea Saab, Aiman S Winkler, Ulrike Marx, Grit Imamura, Hiromi Möbius, Wiebke Kusch, Kathrin Nave, Klaus-Armin Hirrlinger, Johannes eLife Neuroscience In several neurodegenerative diseases and myelin disorders, the degeneration profiles of myelinated axons are compatible with underlying energy deficits. However, it is presently impossible to measure selectively axonal ATP levels in the electrically active nervous system. We combined transgenic expression of an ATP-sensor in neurons of mice with confocal FRET imaging and electrophysiological recordings of acutely isolated optic nerves. This allowed us to monitor dynamic changes and activity-dependent axonal ATP homeostasis at the cellular level and in real time. We find that changes in ATP levels correlate well with compound action potentials. However, this correlation is disrupted when metabolism of lactate is inhibited, suggesting that axonal glycolysis products are not sufficient to maintain mitochondrial energy metabolism of electrically active axons. The combined monitoring of cellular ATP and electrical activity is a novel tool to study neuronal and glial energy metabolism in normal physiology and in models of neurodegenerative disorders. DOI: http://dx.doi.org/10.7554/eLife.24241.001 eLife Sciences Publications, Ltd 2017-04-17 /pmc/articles/PMC5415357/ /pubmed/28414271 http://dx.doi.org/10.7554/eLife.24241 Text en © 2017, Trevisiol et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Trevisiol, Andrea Saab, Aiman S Winkler, Ulrike Marx, Grit Imamura, Hiromi Möbius, Wiebke Kusch, Kathrin Nave, Klaus-Armin Hirrlinger, Johannes Monitoring ATP dynamics in electrically active white matter tracts |
title | Monitoring ATP dynamics in electrically active white matter tracts |
title_full | Monitoring ATP dynamics in electrically active white matter tracts |
title_fullStr | Monitoring ATP dynamics in electrically active white matter tracts |
title_full_unstemmed | Monitoring ATP dynamics in electrically active white matter tracts |
title_short | Monitoring ATP dynamics in electrically active white matter tracts |
title_sort | monitoring atp dynamics in electrically active white matter tracts |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415357/ https://www.ncbi.nlm.nih.gov/pubmed/28414271 http://dx.doi.org/10.7554/eLife.24241 |
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