| Literature DB >> 27264177 |
Natale R Sciolino1, Nicholas W Plummer1, Yu-Wei Chen1, Georgia M Alexander1, Sabrina D Robertson2, Serena M Dudek1, Zoe A McElligott3, Patricia Jensen4.
Abstract
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. Published by Elsevier Inc.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27264177 PMCID: PMC4915594 DOI: 10.1016/j.celrep.2016.05.034
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423