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Recombinase-Dependent Mouse Lines for Chemogenetic Activation of Genetically Defined Cell Types
Author(s) -
Natale R. Sciolino,
Nicholas W. Plummer,
Yuwei Chen,
Georgia M. Alexander,
Sabrina D. Robertson,
Serena M. Dudek,
Zoé A. McElligott,
Patricia Jensen
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.05.034
Subject(s) - biology , recombinase , phenotype , cre recombinase , microbiology and biotechnology , cell type , locus coeruleus , transgene , allele , neuroscience , cell , genetically modified mouse , genetics , central nervous system , gene , recombination
Chemogenetic technologies, including the mutated human Gq-coupled M3 muscarinic receptor (hM3Dq), have greatly facilitated our ability to directly link changes in cellular activity to altered physiology and behavior. Here, we extend the hM3Dq toolkit with recombinase-responsive mouse lines that permit hM3Dq expression in virtually any cell type. These alleles encode a fusion protein designed to increase effective expression levels by concentrating hM3Dq to the cell body and dendrites. To illustrate their broad utility, we targeted three different genetically defined cell populations: noradrenergic neurons of the compact, bilateral locus coeruleus and two dispersed populations, Camk2a+ neurons and GFAP+ glia. In all three populations, we observed reproducible expression and confirmed that activation of hM3Dq is sufficient to dose-dependently evoke phenotypic changes, without extreme phenotypes associated with hM3Dq overexpression. These alleles offer the ability to non-invasively control activity of diverse cell types to uncover their function and dysfunction at any developmental stage.

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