RT Journal Article SR Electronic T1 Genetic engineering for in vivo optical interrogation of neuronal responses to cell type-specific silencing JF bioRxiv FD Cold Spring Harbor Laboratory SP 2021.01.13.426508 DO 10.1101/2021.01.13.426508 A1 Terzi, Firat A1 Knabbe, Johannes A1 Cambridge, Sidney B. YR 2021 UL http://biorxiv.org/content/early/2021/01/14/2021.01.13.426508.abstract AB Genetic engineering of quintuple transgenic brain tissue was used to establish a low background, Cre-dependent version of the inducible Tet-On system for fast, cell type-specific transgene expression in vivo. Co-expression of a constitutive, Cre-dependent fluorescent marker selectively allowed single cell analyses before and after inducible, tet-dependent transgene expression. Here, we used this method for acute, high-resolution manipulation of neuronal activity in the living brain. Single induction of the potassium channel Kir2.1 produced cell type-specific silencing within hours that lasted for at least three days. Longitudinal in vivo imaging of spontaneous calcium transients and neuronal morphology demonstrated that prolonged silencing did not alter spine densities or synaptic input strength. Furthermore, selective induction of Kir2.1 in parvalbumin interneurons increased the activity of surrounding neurons in a distance-dependent manner. This high-resolution, inducible interference and interval imaging of individual cells (high I5, ‘HighFive’) method thus allows visualizing temporally precise, genetic perturbations of defined cells.Competing Interest StatementThe authors have declared no competing interest.