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Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity

Optogenetics is a powerful tool for manipulating neuronal activity by light illumination with high temporal and spatial resolution. Anion-channelrhodopsins (ACRs) are light-gated anion channels that allow researchers to efficiently inhibit neuronal activity. A blue light-sensitive ACR2 has recently...

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Autores principales: Mukai, Yasutaka, Li, Yan, Nakamura, Akiyo, Fukatsu, Noriaki, Iijima, Daisuke, Abe, Manabu, Sakimura, Kenji, Itoi, Keiichi, Yamanaka, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998869/
https://www.ncbi.nlm.nih.gov/pubmed/36894577
http://dx.doi.org/10.1038/s41598-023-30907-2
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author Mukai, Yasutaka
Li, Yan
Nakamura, Akiyo
Fukatsu, Noriaki
Iijima, Daisuke
Abe, Manabu
Sakimura, Kenji
Itoi, Keiichi
Yamanaka, Akihiro
author_facet Mukai, Yasutaka
Li, Yan
Nakamura, Akiyo
Fukatsu, Noriaki
Iijima, Daisuke
Abe, Manabu
Sakimura, Kenji
Itoi, Keiichi
Yamanaka, Akihiro
author_sort Mukai, Yasutaka
collection PubMed
description Optogenetics is a powerful tool for manipulating neuronal activity by light illumination with high temporal and spatial resolution. Anion-channelrhodopsins (ACRs) are light-gated anion channels that allow researchers to efficiently inhibit neuronal activity. A blue light-sensitive ACR2 has recently been used in several in vivo studies; however, the reporter mouse strain expressing ACR2 has not yet been reported. Here, we generated a new reporter mouse strain, LSL-ACR2, in which ACR2 is expressed under the control of Cre recombinase. We crossed this strain with a noradrenergic neuron-specific driver mouse (NAT-Cre) to generate NAT-ACR2 mice. We confirmed Cre-dependent expression and function of ACR2 in the targeted neurons by immunohistochemistry and electrophysiological recordings in vitro, and confirmed physiological function using an in vivo behavioral experiment. Our results show that the LSL-ACR2 mouse strain can be applied for optogenetic inhibition of targeted neurons, particularly for long-lasting continuous inhibition, upon crossing with Cre-driver mouse strains. The LSL-ACR2 strain can be used to prepare transgenic mice with homogenous expression of ACR2 in targeted neurons with a high penetration ratio, good reproducibility, and no tissue invasion.
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spelling pubmed-99988692023-03-11 Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity Mukai, Yasutaka Li, Yan Nakamura, Akiyo Fukatsu, Noriaki Iijima, Daisuke Abe, Manabu Sakimura, Kenji Itoi, Keiichi Yamanaka, Akihiro Sci Rep Article Optogenetics is a powerful tool for manipulating neuronal activity by light illumination with high temporal and spatial resolution. Anion-channelrhodopsins (ACRs) are light-gated anion channels that allow researchers to efficiently inhibit neuronal activity. A blue light-sensitive ACR2 has recently been used in several in vivo studies; however, the reporter mouse strain expressing ACR2 has not yet been reported. Here, we generated a new reporter mouse strain, LSL-ACR2, in which ACR2 is expressed under the control of Cre recombinase. We crossed this strain with a noradrenergic neuron-specific driver mouse (NAT-Cre) to generate NAT-ACR2 mice. We confirmed Cre-dependent expression and function of ACR2 in the targeted neurons by immunohistochemistry and electrophysiological recordings in vitro, and confirmed physiological function using an in vivo behavioral experiment. Our results show that the LSL-ACR2 mouse strain can be applied for optogenetic inhibition of targeted neurons, particularly for long-lasting continuous inhibition, upon crossing with Cre-driver mouse strains. The LSL-ACR2 strain can be used to prepare transgenic mice with homogenous expression of ACR2 in targeted neurons with a high penetration ratio, good reproducibility, and no tissue invasion. Nature Publishing Group UK 2023-03-09 /pmc/articles/PMC9998869/ /pubmed/36894577 http://dx.doi.org/10.1038/s41598-023-30907-2 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mukai, Yasutaka
Li, Yan
Nakamura, Akiyo
Fukatsu, Noriaki
Iijima, Daisuke
Abe, Manabu
Sakimura, Kenji
Itoi, Keiichi
Yamanaka, Akihiro
Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity
title Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity
title_full Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity
title_fullStr Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity
title_full_unstemmed Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity
title_short Cre-dependent ACR2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity
title_sort cre-dependent acr2-expressing reporter mouse strain for efficient long-lasting inhibition of neuronal activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998869/
https://www.ncbi.nlm.nih.gov/pubmed/36894577
http://dx.doi.org/10.1038/s41598-023-30907-2
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