| dc.contributor.author | Zhao, Shengli | |
| dc.contributor.author | Ting, Jonathan Thomas | |
| dc.contributor.author | Atallah, Hicham | |
| dc.contributor.author | Qiu, Li | |
| dc.contributor.author | Tan, Jie | |
| dc.contributor.author | Gloss, Bernd | |
| dc.contributor.author | Augustine, George J. | |
| dc.contributor.author | Deisseroth, Karl | |
| dc.contributor.author | Luo, Minmin | |
| dc.contributor.author | Graybiel, Ann M. | |
| dc.contributor.author | Feng, Guoping | |
| dc.date.accessioned | 2012-06-28T13:38:15Z | |
| dc.date.available | 2012-06-28T13:38:15Z | |
| dc.date.issued | 2011-10 | |
| dc.identifier.issn | 1548-7091 | |
| dc.identifier.issn | 1548-7105 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/71248 | |
| dc.description.abstract | 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. | en_US |
| dc.description.sponsorship | National Institutes of Health (U.S.) (Ruth L. Kirschstein National Research Service award (F32MH084460)) | en_US |
| dc.description.sponsorship | National Institute of Mental Health (U.S.) (RC1-MH088434) | en_US |
| dc.description.sponsorship | Brain and Behavior Research Foundation (Young Investigator award) | en_US |
| dc.language.iso | en_US | |
| dc.publisher | Nature Publishing Group | en_US |
| dc.relation.isversionof | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191888/pdf/nihms-311754.pdf?tool=pmcentrez | en_US |
| dc.rights | 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. | en_US |
| dc.rights.uri | | en_US |
| dc.source | PubMed Central | en_US |
| dc.title | Cell-type Specific Optogenetic Mice for Dissecting Neural Circuitry Function | en_US |
| dc.title.alternative | Cell type–specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function | en_US |
| dc.type | Article | en_US |
| dc.identifier.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. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | en_US |
| dc.contributor.department | McGovern Institute for Brain Research at MIT | en_US |
| dc.contributor.approver | Feng, Guoping | |
| dc.contributor.mitauthor | Feng, Guoping | |
| dc.contributor.mitauthor | Atallah, Hicham | |
| dc.contributor.mitauthor | Ting, Jonathan Thomas | |
| dc.contributor.mitauthor | Graybiel, Ann M. | |
| dc.relation.journal | Nature Methods | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dspace.orderedauthors | Zhao, Shengli; Ting, Jonathan T.; Atallah, Hisham E.; Qiu, Li; Tan, Jie; Gloss, Bernd; Augustine, George J.; Deisseroth, Karl; Luo, Minmin; Graybiel, Ann M.; Feng, Guoping | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0002-8021-277X | |
| dc.identifier.orcid | https://orcid.org/0000-0002-4326-7720 | |
| mit.license | PUBLISHER_POLICY | en_US |
| mit.metadata.status | Complete | |