Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells

Dopamine cells in the ventral tegmental area (VTADA) are critical for a variety of motivated behaviors. These cells receive synaptic inputs from over 100 anatomically defined brain regions, which enables control from a distributed set of inputs across the brain. Extensive efforts have been made to m...

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Main Author: Kevin Beier
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2022-05-01
Series:eLife
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Online Access:https://elifesciences.org/articles/76886
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author Kevin Beier
author_facet Kevin Beier
author_sort Kevin Beier
collection DOAJ
description Dopamine cells in the ventral tegmental area (VTADA) are critical for a variety of motivated behaviors. These cells receive synaptic inputs from over 100 anatomically defined brain regions, which enables control from a distributed set of inputs across the brain. Extensive efforts have been made to map inputs to VTA cells based on neurochemical phenotype and output site. However, all of these studies have the same fundamental limitation that inputs local to the VTA cannot be properly assessed due to non-Cre-dependent uptake of EnvA-pseudotyped virus. Therefore, the quantitative contribution of local inputs to the VTA, including GABAergic, DAergic, and serotonergic, is not known. Here, I used a modified viral-genetic strategy that enables examination of both local and long-range inputs to VTADA cells in mice. I found that nearly half of the total inputs to VTADA cells are located locally, revealing a substantial portion of inputs that have been missed by previous analyses. The majority of inhibition to VTADA cells arises from the substantia nigra pars reticulata, with large contributions from the VTA and the substantia nigra pars compacta. In addition to receiving inputs from VTAGABA neurons, DA neurons are connected with other DA neurons within the VTA as well as the nearby retrorubal field. Lastly, I show that VTADA neurons receive inputs from distributed serotonergic neurons throughout the midbrain and hindbrain, with the majority arising from the dorsal raphe. My study highlights the importance of using the appropriate combination of viral-genetic reagents to unmask the complexity of connectivity relationships to defined cells in the brain.
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spelling doaj.art-0d877b4f9eab4ac69256e022f53b89582022-12-22T02:05:33ZengeLife Sciences Publications LtdeLife2050-084X2022-05-011110.7554/eLife.76886Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cellsKevin Beier0https://orcid.org/0000-0002-4934-1338Department of Physiology and Biophysics, Neurobiology and Behavior, Biomedical Engineering, Pharmaceutical Sciences, Center for the Neurobiology of Learning and Memory, University of California, Irvine, Irvine, United StatesDopamine cells in the ventral tegmental area (VTADA) are critical for a variety of motivated behaviors. These cells receive synaptic inputs from over 100 anatomically defined brain regions, which enables control from a distributed set of inputs across the brain. Extensive efforts have been made to map inputs to VTA cells based on neurochemical phenotype and output site. However, all of these studies have the same fundamental limitation that inputs local to the VTA cannot be properly assessed due to non-Cre-dependent uptake of EnvA-pseudotyped virus. Therefore, the quantitative contribution of local inputs to the VTA, including GABAergic, DAergic, and serotonergic, is not known. Here, I used a modified viral-genetic strategy that enables examination of both local and long-range inputs to VTADA cells in mice. I found that nearly half of the total inputs to VTADA cells are located locally, revealing a substantial portion of inputs that have been missed by previous analyses. The majority of inhibition to VTADA cells arises from the substantia nigra pars reticulata, with large contributions from the VTA and the substantia nigra pars compacta. In addition to receiving inputs from VTAGABA neurons, DA neurons are connected with other DA neurons within the VTA as well as the nearby retrorubal field. Lastly, I show that VTADA neurons receive inputs from distributed serotonergic neurons throughout the midbrain and hindbrain, with the majority arising from the dorsal raphe. My study highlights the importance of using the appropriate combination of viral-genetic reagents to unmask the complexity of connectivity relationships to defined cells in the brain.https://elifesciences.org/articles/76886dopaminerabiesmonosynaptic tracingventral tegmental areainhibition
spellingShingle Kevin Beier
Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells
eLife
dopamine
rabies
monosynaptic tracing
ventral tegmental area
inhibition
title Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells
title_full Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells
title_fullStr Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells
title_full_unstemmed Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells
title_short Modified viral-genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells
title_sort modified viral genetic mapping reveals local and global connectivity relationships of ventral tegmental area dopamine cells
topic dopamine
rabies
monosynaptic tracing
ventral tegmental area
inhibition
url https://elifesciences.org/articles/76886
work_keys_str_mv AT kevinbeier modifiedviralgeneticmappingrevealslocalandglobalconnectivityrelationshipsofventraltegmentalareadopaminecells