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Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro

Ruthenium–bipyridinetriphenylphosphine–GABA (RuBi–GABA) is a caged compound that allows studying the neuronal transmission in a specific region of a neuron. The inhibitory neurotransmitter γ-aminobutyric acid (GABA) is bound to a caged group that blocks the interaction of the neurotransmitter with i...

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Autores principales: Cozzolino, Marco, Bazzurro, Virginia, Gatta, Elena, Bianchini, Paolo, Angeli, Elena, Robello, Mauro, Diaspro, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414112/
https://www.ncbi.nlm.nih.gov/pubmed/32770032
http://dx.doi.org/10.1038/s41598-020-70217-5
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author Cozzolino, Marco
Bazzurro, Virginia
Gatta, Elena
Bianchini, Paolo
Angeli, Elena
Robello, Mauro
Diaspro, Alberto
author_facet Cozzolino, Marco
Bazzurro, Virginia
Gatta, Elena
Bianchini, Paolo
Angeli, Elena
Robello, Mauro
Diaspro, Alberto
author_sort Cozzolino, Marco
collection PubMed
description Ruthenium–bipyridinetriphenylphosphine–GABA (RuBi–GABA) is a caged compound that allows studying the neuronal transmission in a specific region of a neuron. The inhibitory neurotransmitter γ-aminobutyric acid (GABA) is bound to a caged group that blocks the interaction of the neurotransmitter with its receptor site. Following linear—one-photon (1P)—and non-linear—multi-photon—absorption of light, the covalent bond of the caged molecule is broken, and GABA is released. Such a controlled release in time and space allows investigating the interaction with its receptor in four dimensions (X,Y,Z,t). Taking advantage of this strategy, we succeeded in addressing the modulation of GABA(A) in rat cerebellar neurons by coupling the photoactivation process, by confocal or two-photon excitation microscopy, with the electrophysiological technique of the patch-clamp in the whole-cell configuration. Key parameters have been comprehensively investigated and correlated in a temporally and spatially confined way, namely: photoactivation laser power, time of exposure, and distance of the uncaging point from the cell of interest along the X, Y, Z spatial coordinates. The goal of studying specific biological events as a function of controlled physical parameters has been achieved.
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spelling pubmed-74141122020-08-10 Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro Cozzolino, Marco Bazzurro, Virginia Gatta, Elena Bianchini, Paolo Angeli, Elena Robello, Mauro Diaspro, Alberto Sci Rep Article Ruthenium–bipyridinetriphenylphosphine–GABA (RuBi–GABA) is a caged compound that allows studying the neuronal transmission in a specific region of a neuron. The inhibitory neurotransmitter γ-aminobutyric acid (GABA) is bound to a caged group that blocks the interaction of the neurotransmitter with its receptor site. Following linear—one-photon (1P)—and non-linear—multi-photon—absorption of light, the covalent bond of the caged molecule is broken, and GABA is released. Such a controlled release in time and space allows investigating the interaction with its receptor in four dimensions (X,Y,Z,t). Taking advantage of this strategy, we succeeded in addressing the modulation of GABA(A) in rat cerebellar neurons by coupling the photoactivation process, by confocal or two-photon excitation microscopy, with the electrophysiological technique of the patch-clamp in the whole-cell configuration. Key parameters have been comprehensively investigated and correlated in a temporally and spatially confined way, namely: photoactivation laser power, time of exposure, and distance of the uncaging point from the cell of interest along the X, Y, Z spatial coordinates. The goal of studying specific biological events as a function of controlled physical parameters has been achieved. Nature Publishing Group UK 2020-08-07 /pmc/articles/PMC7414112/ /pubmed/32770032 http://dx.doi.org/10.1038/s41598-020-70217-5 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
Cozzolino, Marco
Bazzurro, Virginia
Gatta, Elena
Bianchini, Paolo
Angeli, Elena
Robello, Mauro
Diaspro, Alberto
Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro
title Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro
title_full Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro
title_fullStr Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro
title_full_unstemmed Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro
title_short Precise 3D modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro
title_sort precise 3d modulation of electro-optical parameters during neurotransmitter uncaging experiments with neurons in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7414112/
https://www.ncbi.nlm.nih.gov/pubmed/32770032
http://dx.doi.org/10.1038/s41598-020-70217-5
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