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Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks

Opn7b is a non-visual G protein-coupled receptor expressed in zebrafish. Here we find that Opn7b expressed in HEK cells constitutively activates the G(i/o) pathway and illumination with blue/green light inactivates G protein-coupled inwardly rectifying potassium channels. This suggests that light ac...

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Autores principales: Karapinar, Raziye, Schwitalla, Jan Claudius, Eickelbeck, Dennis, Pakusch, Johanna, Mücher, Brix, Grömmke, Michelle, Surdin, Tatjana, Knöpfel, Thomas, Mark, Melanie D., Siveke, Ida, Herlitze, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302595/
https://www.ncbi.nlm.nih.gov/pubmed/34301944
http://dx.doi.org/10.1038/s41467-021-24718-0
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author Karapinar, Raziye
Schwitalla, Jan Claudius
Eickelbeck, Dennis
Pakusch, Johanna
Mücher, Brix
Grömmke, Michelle
Surdin, Tatjana
Knöpfel, Thomas
Mark, Melanie D.
Siveke, Ida
Herlitze, Stefan
author_facet Karapinar, Raziye
Schwitalla, Jan Claudius
Eickelbeck, Dennis
Pakusch, Johanna
Mücher, Brix
Grömmke, Michelle
Surdin, Tatjana
Knöpfel, Thomas
Mark, Melanie D.
Siveke, Ida
Herlitze, Stefan
author_sort Karapinar, Raziye
collection PubMed
description Opn7b is a non-visual G protein-coupled receptor expressed in zebrafish. Here we find that Opn7b expressed in HEK cells constitutively activates the G(i/o) pathway and illumination with blue/green light inactivates G protein-coupled inwardly rectifying potassium channels. This suggests that light acts as an inverse agonist for Opn7b and can be used as an optogenetic tool to inhibit neuronal networks in the dark and interrupt constitutive inhibition in the light. Consistent with this prediction, illumination of recombinant expressed Opn7b in cortical pyramidal cells results in increased neuronal activity. In awake mice, light stimulation of Opn7b expressed in pyramidal cells of somatosensory cortex reliably induces generalized epileptiform activity within a short (<10 s) delay after onset of stimulation. Our study demonstrates a reversed mechanism for G protein-coupled receptor control and Opn7b as a tool for controlling neural circuit properties.
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spelling pubmed-83025952021-08-12 Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks Karapinar, Raziye Schwitalla, Jan Claudius Eickelbeck, Dennis Pakusch, Johanna Mücher, Brix Grömmke, Michelle Surdin, Tatjana Knöpfel, Thomas Mark, Melanie D. Siveke, Ida Herlitze, Stefan Nat Commun Article Opn7b is a non-visual G protein-coupled receptor expressed in zebrafish. Here we find that Opn7b expressed in HEK cells constitutively activates the G(i/o) pathway and illumination with blue/green light inactivates G protein-coupled inwardly rectifying potassium channels. This suggests that light acts as an inverse agonist for Opn7b and can be used as an optogenetic tool to inhibit neuronal networks in the dark and interrupt constitutive inhibition in the light. Consistent with this prediction, illumination of recombinant expressed Opn7b in cortical pyramidal cells results in increased neuronal activity. In awake mice, light stimulation of Opn7b expressed in pyramidal cells of somatosensory cortex reliably induces generalized epileptiform activity within a short (<10 s) delay after onset of stimulation. Our study demonstrates a reversed mechanism for G protein-coupled receptor control and Opn7b as a tool for controlling neural circuit properties. Nature Publishing Group UK 2021-07-23 /pmc/articles/PMC8302595/ /pubmed/34301944 http://dx.doi.org/10.1038/s41467-021-24718-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Karapinar, Raziye
Schwitalla, Jan Claudius
Eickelbeck, Dennis
Pakusch, Johanna
Mücher, Brix
Grömmke, Michelle
Surdin, Tatjana
Knöpfel, Thomas
Mark, Melanie D.
Siveke, Ida
Herlitze, Stefan
Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks
title Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks
title_full Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks
title_fullStr Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks
title_full_unstemmed Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks
title_short Reverse optogenetics of G protein signaling by zebrafish non-visual opsin Opn7b for synchronization of neuronal networks
title_sort reverse optogenetics of g protein signaling by zebrafish non-visual opsin opn7b for synchronization of neuronal networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302595/
https://www.ncbi.nlm.nih.gov/pubmed/34301944
http://dx.doi.org/10.1038/s41467-021-24718-0
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