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Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity

Several recently developed Channelrhodopsin (ChR) variants are characterized by rapid kinetics and reduced desensitization in comparison to the widely used ChR2. However, little is known about how varying opsin properties may regulate their interaction with local network dynamics. We compared evoked...

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Autores principales: Jun, Na Young, Cardin, Jessica A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944482/
https://www.ncbi.nlm.nih.gov/pubmed/31822522
http://dx.doi.org/10.1523/ENEURO.0222-18.2019
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author Jun, Na Young
Cardin, Jessica A.
author_facet Jun, Na Young
Cardin, Jessica A.
author_sort Jun, Na Young
collection PubMed
description Several recently developed Channelrhodopsin (ChR) variants are characterized by rapid kinetics and reduced desensitization in comparison to the widely used ChR2. However, little is known about how varying opsin properties may regulate their interaction with local network dynamics. We compared evoked cortical activity in mice expressing three ChR variants with distinct temporal profiles under the CamKII promoter: Chronos, Chrimson, and ChR2. We assessed overall neural activation by measuring the amplitude and temporal progression of evoked spiking. Using γ-range (30–80 Hz) local field potential (LFP) power as an assay for local network engagement, we examined the recruitment of cortical network activity by each tool. All variants caused light-evoked increases in firing in vivo, but each demonstrated different temporal patterning of evoked activity. In addition, the three ChRs had distinct effects on cortical γ-band activity. Our findings suggest the properties of optogenetic tools can substantially affect their efficacy in vivo, as well their engagement of circuit resonance.
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spelling pubmed-69444822020-01-07 Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity Jun, Na Young Cardin, Jessica A. eNeuro New Research Several recently developed Channelrhodopsin (ChR) variants are characterized by rapid kinetics and reduced desensitization in comparison to the widely used ChR2. However, little is known about how varying opsin properties may regulate their interaction with local network dynamics. We compared evoked cortical activity in mice expressing three ChR variants with distinct temporal profiles under the CamKII promoter: Chronos, Chrimson, and ChR2. We assessed overall neural activation by measuring the amplitude and temporal progression of evoked spiking. Using γ-range (30–80 Hz) local field potential (LFP) power as an assay for local network engagement, we examined the recruitment of cortical network activity by each tool. All variants caused light-evoked increases in firing in vivo, but each demonstrated different temporal patterning of evoked activity. In addition, the three ChRs had distinct effects on cortical γ-band activity. Our findings suggest the properties of optogenetic tools can substantially affect their efficacy in vivo, as well their engagement of circuit resonance. Society for Neuroscience 2020-01-02 /pmc/articles/PMC6944482/ /pubmed/31822522 http://dx.doi.org/10.1523/ENEURO.0222-18.2019 Text en Copyright © 2020 Jun and Cardin http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Jun, Na Young
Cardin, Jessica A.
Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity
title Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity
title_full Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity
title_fullStr Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity
title_full_unstemmed Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity
title_short Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity
title_sort activation of distinct channelrhodopsin variants engages different patterns of network activity
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944482/
https://www.ncbi.nlm.nih.gov/pubmed/31822522
http://dx.doi.org/10.1523/ENEURO.0222-18.2019
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