Author:
Mukai Yasutaka,Li Yan,Nakamura Akiyo,Fukatsu Noriaki,Iijima Daisuke,Abe Manabu,Sakimura Kenji,Itoi Keiichi,Yamanaka Akihiro
Abstract
AbstractOptogenetics 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.
Funder
Japan Society for the Promotion of Science
AMED-CREST
Mitsubishi Foundation
SENSHIN Medical Research Foundation
Kao Foundation for Arts and Sciences
Lotte Foundation
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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