Cell Reports · 2016 · 126 citations · 27 references
Life SciencesNeurobiologyNeuroscienceCellular NeuroscienceMolecular NeurobiologyMolecular NeuroscienceCell Signaling In NeuronsMolecular NeurogeneticsNeurotransmissionNeurotransmitter ReceptorsReceptor Signaling In NeuronsSynaptic TransmissionCell Type SpecificityLocus Coeruleus CircuitsMuscarinic Acetylcholine Receptor SignalingMuscarinic Receptor PharmacologyMuscarinic Receptor SubtypesMuscarinic ReceptorsNoradrenergic CircuitsNoradrenergic Neurotransmission
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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Blaine N. Armbruster, Xiang Li, Mark H. Pausch et al. · Proceedings of the National Academy of Sciences · 2007 · 2.1K citations · Full text
Subregion- and Cell Type–Restricted Gene Knockout in Mouse Brain
Joe Z. Tsien, Dong Feng Chen, David J. Gerber et al. · Cell · 1996 · 1.3K citations · Full text