Cell-type Specific Optogenetic Mice for Dissecting Neural Circuitry Function
Author(s)
Zhao, Shengli; Ting, Jonathan Thomas; Atallah, Hicham; Qiu, Li; Tan, Jie; Gloss, Bernd; Augustine, George J.; Deisseroth, Karl; Luo, Minmin; Graybiel, Ann M.; Feng, Guoping; ... Show more Show less
DownloadFeng-Cell-type Specific Optogenetic.pdf (1.964Mb)
PUBLISHER_POLICY
Publisher Policy
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Alternative title
Cell type–specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function
Terms of use
Metadata
Show full item recordAbstract
Optogenetic methods have emerged as powerful tools for dissecting neural circuit connectivity, function, and dysfunction. We used a Bacterial Artificial Chromosome (BAC) transgenic strategy to express Channelrhodopsin2 (ChR2) under the control of cell-type specific promoter elements. We provide a detailed functional characterization of the newly established VGAT-ChR2-EYFP, ChAT-ChR2-EYFP, TPH2-ChR2-EYFP and Pvalb-ChR2-EYFP BAC transgenic mouse lines and demonstrate the utility of these lines for precisely controlling action potential firing of GABAergic, cholinergic, serotonergic, and parvalbumin+ neuron subsets using blue light. This resource of cell type-specific ChR2 mouse lines will facilitate the precise mapping of neuronal connectivity and the dissection of the neural basis of behavior.
Date issued
2011-10Department
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences; McGovern Institute for Brain Research at MITJournal
Nature Methods
Publisher
Nature Publishing Group
Citation
Zhao, Shengli et al. "Cell type–specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function." Nature Methods, 2011 ; 8(9): 745–752.
Version: Author's final manuscript
ISSN
1548-7091
1548-7105