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Genetically encoded proton sensors reveal activity-dependent pH changes in neurons
The regulation of hydrogen ion concentration (pH) is fundamental to cell viability, metabolism, and enzymatic function. Within the nervous system, the control of pH is also involved in diverse and dynamic processes including development, synaptic transmission, and the control of network excitability...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364509/ https://www.ncbi.nlm.nih.gov/pubmed/22666186 http://dx.doi.org/10.3389/fnmol.2012.00068 |
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author | Raimondo, Joseph V. Irkle, Agnese Wefelmeyer, Winnie Newey, Sarah E. Akerman, Colin J. |
author_facet | Raimondo, Joseph V. Irkle, Agnese Wefelmeyer, Winnie Newey, Sarah E. Akerman, Colin J. |
author_sort | Raimondo, Joseph V. |
collection | PubMed |
description | The regulation of hydrogen ion concentration (pH) is fundamental to cell viability, metabolism, and enzymatic function. Within the nervous system, the control of pH is also involved in diverse and dynamic processes including development, synaptic transmission, and the control of network excitability. As pH affects neuronal activity, and can also itself be altered by neuronal activity, the existence of tools to accurately measure hydrogen ion fluctuations is important for understanding the role pH plays under physiological and pathological conditions. Outside of their use as a marker of synaptic release, genetically encoded pH sensors have not been utilized to study hydrogen ion fluxes associated with network activity. By combining whole-cell patch clamp with simultaneous two-photon or confocal imaging, we quantified the amplitude and time course of neuronal, intracellular, acidic transients evoked by epileptiform activity in two separate in vitro models of temporal lobe epilepsy. In doing so, we demonstrate the suitability of three genetically encoded pH sensors: deGFP4, E(2)GFP, and Cl-sensor for investigating activity-dependent pH changes at the level of single neurons. |
format | Online Article Text |
id | pubmed-3364509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-33645092012-06-04 Genetically encoded proton sensors reveal activity-dependent pH changes in neurons Raimondo, Joseph V. Irkle, Agnese Wefelmeyer, Winnie Newey, Sarah E. Akerman, Colin J. Front Mol Neurosci Neuroscience The regulation of hydrogen ion concentration (pH) is fundamental to cell viability, metabolism, and enzymatic function. Within the nervous system, the control of pH is also involved in diverse and dynamic processes including development, synaptic transmission, and the control of network excitability. As pH affects neuronal activity, and can also itself be altered by neuronal activity, the existence of tools to accurately measure hydrogen ion fluctuations is important for understanding the role pH plays under physiological and pathological conditions. Outside of their use as a marker of synaptic release, genetically encoded pH sensors have not been utilized to study hydrogen ion fluxes associated with network activity. By combining whole-cell patch clamp with simultaneous two-photon or confocal imaging, we quantified the amplitude and time course of neuronal, intracellular, acidic transients evoked by epileptiform activity in two separate in vitro models of temporal lobe epilepsy. In doing so, we demonstrate the suitability of three genetically encoded pH sensors: deGFP4, E(2)GFP, and Cl-sensor for investigating activity-dependent pH changes at the level of single neurons. Frontiers Media S.A. 2012-05-31 /pmc/articles/PMC3364509/ /pubmed/22666186 http://dx.doi.org/10.3389/fnmol.2012.00068 Text en Copyright © 2012 Raimondo, Irkle, Wefelmeyer, Newey and Akerman. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Neuroscience Raimondo, Joseph V. Irkle, Agnese Wefelmeyer, Winnie Newey, Sarah E. Akerman, Colin J. Genetically encoded proton sensors reveal activity-dependent pH changes in neurons |
title | Genetically encoded proton sensors reveal activity-dependent pH changes in neurons |
title_full | Genetically encoded proton sensors reveal activity-dependent pH changes in neurons |
title_fullStr | Genetically encoded proton sensors reveal activity-dependent pH changes in neurons |
title_full_unstemmed | Genetically encoded proton sensors reveal activity-dependent pH changes in neurons |
title_short | Genetically encoded proton sensors reveal activity-dependent pH changes in neurons |
title_sort | genetically encoded proton sensors reveal activity-dependent ph changes in neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364509/ https://www.ncbi.nlm.nih.gov/pubmed/22666186 http://dx.doi.org/10.3389/fnmol.2012.00068 |
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