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Cited 12 time in webofscience Cited 10 time in scopus
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Viral labeling of neurons synaptically connected to nucleus accumbens somatostatin interneurons

Authors
Ribeiro, Efrain A.Nectow, Alexander R.Pomeranz, Lisa E.Ekstrand, Mats I.Koo, Ja WookNestler, Eric J.
Issue Date
Mar-2019
Publisher
PUBLIC LIBRARY SCIENCE
Citation
PLOS ONE, v.14, no.3
Journal Title
PLOS ONE
Volume
14
Number
3
URI
http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/699
DOI
10.1371/journal.pone.0213476
ISSN
1932-6203
Abstract
The nucleus accumbens, a key brain reward region, receives synaptic inputs from a range of forebrain and brainstem regions. Many of these projections have been established using electrophysiology or fluorescent tract tracing. However, more recently developed viral tracing techniques have allowed for fluorescent labeling of synaptic afferents in a cell type-specific manner. Since the NAc is comprised of multiple cell types, these methods have enabled the delineation of the cell type-specific connectivity of principal medium spiny neurons in the region. The synaptic connectivity of somatostatin interneurons, which account for <5% of the neurons in the region, has been inferred from electrophysiological and immunohistochemical data, but has not yet been visualized using modern viral tracing techniques. Here, we use the pseudorabies virus (PRV)-Introvert-GFP virus, an alphaherpes virus previously shown to label synaptic afferents in a cell type-specific manner, to label first order afferents to NAc somatostatin interneurons. While we find GFP(+) labeling in several well established projections to the NAc, we also observe that several known projections to NAc did not contain GFP(+) cells, suggesting they do not innervate somatostatin interneurons in the region. A subset of the GFP(+) afferents are c-FOS(+) following acute administration of cocaine, showing that NAc somatostatin interneurons are innervated by some cells that respond to rewarding stimuli. These results provide a foundation for future studies aimed toward elucidating the cell type-specific connectivity of the NAc, and identify specific circuits that warrant future functional characterization.
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