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Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup

Chloride (Cl(−)) homeostasis is known to be fundamental for central nervous system functioning. Alterations in intracellular Cl(−) concentration ([Cl(−)](i)) and changes in the efficacy of Cl(−) extrusion are involved in numerous neurological disorders. Therefore, there is a strong need for studies...

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Autores principales: Friedel, Perrine, Bregestovski, Piotr, Medina, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622059/
https://www.ncbi.nlm.nih.gov/pubmed/23596389
http://dx.doi.org/10.3389/fnmol.2013.00007
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author Friedel, Perrine
Bregestovski, Piotr
Medina, Igor
author_facet Friedel, Perrine
Bregestovski, Piotr
Medina, Igor
author_sort Friedel, Perrine
collection PubMed
description Chloride (Cl(−)) homeostasis is known to be fundamental for central nervous system functioning. Alterations in intracellular Cl(−) concentration ([Cl(−)](i)) and changes in the efficacy of Cl(−) extrusion are involved in numerous neurological disorders. Therefore, there is a strong need for studies of the dynamics of [Cl(−)](i) in different cell types under physiological conditions and during pathology. Several previous works reported having successfully achieved recording of [Cl(−)](i) using genetically encoded Cl-Sensor that is composed of the cyan fluorescent protein (CFP) and Cl(−)-sensitive mutant of the yellow fluorescent protein (YFP(Cl)). However, all reported works were performed using specially designed setups with ultra-sensitive CCD cameras. Our multiple attempts to monitor Cl(−)-dependent fluorescence of Cl-Sensor using conventional epifluorescence microscopes did not yield successful results. In the present work, we have analysed the reason of our failures and found that they were caused by a strong inactivation of the YFP(Cl) component of Cl-Sensor during excitation of the CFP with 430 nm light. Based on the obtained results, we reduced 20-fold the intensity of the 430 nm excitation and modified the recording protocol that allows now stable long-lasting ratiometric measurements of Cl-Sensor fluorescence in different cell types including cultured hippocampal neurons and their tiny dendrites and spines. Simultaneous imaging and patch clamp recording revealed that in mature neurons, the novel protocol allows detection of as little as 2 mM changes of [Cl(−)](i) from the resting level of 5–10 mM. We demonstrate also a usefulness of the developed [Cl(−)](i) measurement procedure for large scale screening of the activity of exogenously expressed potassium-chloride co-transporter KCC2, a major neuronal Cl(−) extruder that is implicated in numerous neurological disorders and is a target for novel therapeutical treatments.
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spelling pubmed-36220592013-04-17 Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup Friedel, Perrine Bregestovski, Piotr Medina, Igor Front Mol Neurosci Neuroscience Chloride (Cl(−)) homeostasis is known to be fundamental for central nervous system functioning. Alterations in intracellular Cl(−) concentration ([Cl(−)](i)) and changes in the efficacy of Cl(−) extrusion are involved in numerous neurological disorders. Therefore, there is a strong need for studies of the dynamics of [Cl(−)](i) in different cell types under physiological conditions and during pathology. Several previous works reported having successfully achieved recording of [Cl(−)](i) using genetically encoded Cl-Sensor that is composed of the cyan fluorescent protein (CFP) and Cl(−)-sensitive mutant of the yellow fluorescent protein (YFP(Cl)). However, all reported works were performed using specially designed setups with ultra-sensitive CCD cameras. Our multiple attempts to monitor Cl(−)-dependent fluorescence of Cl-Sensor using conventional epifluorescence microscopes did not yield successful results. In the present work, we have analysed the reason of our failures and found that they were caused by a strong inactivation of the YFP(Cl) component of Cl-Sensor during excitation of the CFP with 430 nm light. Based on the obtained results, we reduced 20-fold the intensity of the 430 nm excitation and modified the recording protocol that allows now stable long-lasting ratiometric measurements of Cl-Sensor fluorescence in different cell types including cultured hippocampal neurons and their tiny dendrites and spines. Simultaneous imaging and patch clamp recording revealed that in mature neurons, the novel protocol allows detection of as little as 2 mM changes of [Cl(−)](i) from the resting level of 5–10 mM. We demonstrate also a usefulness of the developed [Cl(−)](i) measurement procedure for large scale screening of the activity of exogenously expressed potassium-chloride co-transporter KCC2, a major neuronal Cl(−) extruder that is implicated in numerous neurological disorders and is a target for novel therapeutical treatments. Frontiers Media S.A. 2013-04-10 /pmc/articles/PMC3622059/ /pubmed/23596389 http://dx.doi.org/10.3389/fnmol.2013.00007 Text en Copyright © 2013 Friedel, Bregestovski and Medina. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Friedel, Perrine
Bregestovski, Piotr
Medina, Igor
Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup
title Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup
title_full Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup
title_fullStr Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup
title_full_unstemmed Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup
title_short Improved method for efficient imaging of intracellular Cl(−) with Cl-Sensor using conventional fluorescence setup
title_sort improved method for efficient imaging of intracellular cl(−) with cl-sensor using conventional fluorescence setup
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622059/
https://www.ncbi.nlm.nih.gov/pubmed/23596389
http://dx.doi.org/10.3389/fnmol.2013.00007
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