| Literature DB >> 31553913 |
Georg Hafner1, Mirko Witte1, Julien Guy1, Nidhi Subhashini1, Lief E Fenno2, Charu Ramakrishnan2, Yoon Seok Kim2, Karl Deisseroth2, Edward M Callaway3, Martina Oberhuber4, Karl-Klaus Conzelmann4, Jochen F Staiger5.
Abstract
Parvalbumin (PV)-expressing GABAergic neurons are the largest class of inhibitory neocortical cells. We visualize brain-wide, monosynaptic inputs to PV neurons in mouse barrel cortex. We develop intersectional rabies virus tracing to specifically target GABAergic PV cells and exclude a small fraction of excitatory PV cells from our starter population. Local inputs are mainly from layer (L) IV and excitatory cells. A small number of inhibitory inputs originate from LI neurons, which connect to LII/III PV neurons. Long-range inputs originate mainly from other sensory cortices and the thalamus. In visual cortex, most transsynaptically labeled neurons are located in LIV, which contains a molecularly mixed population of projection neurons with putative functional similarity to LIII neurons. This study expands our knowledge of the brain-wide circuits in which PV neurons are embedded and introduces intersectional rabies virus tracing as an applicable tool to dissect the circuitry of more clearly defined cell types.Entities:
Keywords: Cre; Flp; GABAergic neuron; barrel cortex; intersectional; parvalbumin; rabies tracing
Year: 2019 PMID: 31553913 PMCID: PMC6897332 DOI: 10.1016/j.celrep.2019.08.064
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423