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Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy
ANNINE-6 and ANNINE-6plus are voltage-sensitive dyes that when combined with two-photon microscopy are ideal for recording of neuronal voltages in vivo, in both bulk loaded tissue and the dendrites of single neurons. Here, we describe in detail but for a broad audience the voltage sensing mechanism...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646528/ https://www.ncbi.nlm.nih.gov/pubmed/31379507 http://dx.doi.org/10.3389/fncel.2019.00321 |
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author | Kuhn, Bernd Roome, Christopher J. |
author_facet | Kuhn, Bernd Roome, Christopher J. |
author_sort | Kuhn, Bernd |
collection | PubMed |
description | ANNINE-6 and ANNINE-6plus are voltage-sensitive dyes that when combined with two-photon microscopy are ideal for recording of neuronal voltages in vivo, in both bulk loaded tissue and the dendrites of single neurons. Here, we describe in detail but for a broad audience the voltage sensing mechanism of fast voltage-sensitive dyes, with a focus on ANNINE dyes, and how voltage imaging can be optimized with one-photon and two-photon excitation. Under optimized imaging conditions the key strengths of ANNINE dyes are their high sensitivity (0.5%/mV), neglectable bleaching and phototoxicity, a linear response to membrane potential, and a temporal resolution which is faster than the optical imaging devices currently used in neurobiology (order of nanoseconds). ANNINE dyes in combination with two-photon microscopy allow depth-resolved voltage imaging in bulk loaded tissue to study average membrane voltage oscillations and sensory responses. Alternatively, if ANNINE-6plus is applied internally, supra and sub threshold voltage changes can be recorded from dendrites of single neurons in awake animals. Interestingly, in our experience ANNINE-6plus labeling is impressively stable in vivo, such that voltage imaging from single Purkinje neuron dendrites can be performed for 2 weeks after a single electroporation of the neuron. Finally, to maximize their potential for neuroscience studies, voltage imaging with ANNINE dyes and two-photon microscopy can be combined with electrophysiological recording, calcium imaging, and/or pharmacology, even in awake animals. |
format | Online Article Text |
id | pubmed-6646528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66465282019-08-02 Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy Kuhn, Bernd Roome, Christopher J. Front Cell Neurosci Neuroscience ANNINE-6 and ANNINE-6plus are voltage-sensitive dyes that when combined with two-photon microscopy are ideal for recording of neuronal voltages in vivo, in both bulk loaded tissue and the dendrites of single neurons. Here, we describe in detail but for a broad audience the voltage sensing mechanism of fast voltage-sensitive dyes, with a focus on ANNINE dyes, and how voltage imaging can be optimized with one-photon and two-photon excitation. Under optimized imaging conditions the key strengths of ANNINE dyes are their high sensitivity (0.5%/mV), neglectable bleaching and phototoxicity, a linear response to membrane potential, and a temporal resolution which is faster than the optical imaging devices currently used in neurobiology (order of nanoseconds). ANNINE dyes in combination with two-photon microscopy allow depth-resolved voltage imaging in bulk loaded tissue to study average membrane voltage oscillations and sensory responses. Alternatively, if ANNINE-6plus is applied internally, supra and sub threshold voltage changes can be recorded from dendrites of single neurons in awake animals. Interestingly, in our experience ANNINE-6plus labeling is impressively stable in vivo, such that voltage imaging from single Purkinje neuron dendrites can be performed for 2 weeks after a single electroporation of the neuron. Finally, to maximize their potential for neuroscience studies, voltage imaging with ANNINE dyes and two-photon microscopy can be combined with electrophysiological recording, calcium imaging, and/or pharmacology, even in awake animals. Frontiers Media S.A. 2019-07-16 /pmc/articles/PMC6646528/ /pubmed/31379507 http://dx.doi.org/10.3389/fncel.2019.00321 Text en Copyright © 2019 Kuhn and Roome. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kuhn, Bernd Roome, Christopher J. Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy |
title | Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy |
title_full | Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy |
title_fullStr | Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy |
title_full_unstemmed | Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy |
title_short | Primer to Voltage Imaging With ANNINE Dyes and Two-Photon Microscopy |
title_sort | primer to voltage imaging with annine dyes and two-photon microscopy |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646528/ https://www.ncbi.nlm.nih.gov/pubmed/31379507 http://dx.doi.org/10.3389/fncel.2019.00321 |
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