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Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions

Striatal cholinergic (ChAT) and parvalbumin (PV) interneurons exert powerful influences on striatal function in health and disease, yet little is known about the organization of their inputs. Here using rabies tracing, electrophysiology and genetic tools, we compare the whole-brain inputs to these t...

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Autores principales: Klug, Jason R, Engelhardt, Max D, Cadman, Cara N, Li, Hao, Smith, Jared B, Ayala, Sarah, Williams, Elora W, Hoffman, Hilary, Jin, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5929909/
https://www.ncbi.nlm.nih.gov/pubmed/29714166
http://dx.doi.org/10.7554/eLife.35657
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author Klug, Jason R
Engelhardt, Max D
Cadman, Cara N
Li, Hao
Smith, Jared B
Ayala, Sarah
Williams, Elora W
Hoffman, Hilary
Jin, Xin
author_facet Klug, Jason R
Engelhardt, Max D
Cadman, Cara N
Li, Hao
Smith, Jared B
Ayala, Sarah
Williams, Elora W
Hoffman, Hilary
Jin, Xin
author_sort Klug, Jason R
collection PubMed
description Striatal cholinergic (ChAT) and parvalbumin (PV) interneurons exert powerful influences on striatal function in health and disease, yet little is known about the organization of their inputs. Here using rabies tracing, electrophysiology and genetic tools, we compare the whole-brain inputs to these two types of striatal interneurons and dissect their functional connectivity in mice. ChAT interneurons receive a substantial cortical input from associative regions of cortex, such as the orbitofrontal cortex. Amongst subcortical inputs, a previously unknown inhibitory thalamic reticular nucleus input to striatal PV interneurons is identified. Additionally, the external segment of the globus pallidus targets striatal ChAT interneurons, which is sufficient to inhibit tonic ChAT interneuron firing. Finally, we describe a novel excitatory pathway from the pedunculopontine nucleus that innervates ChAT interneurons. These results establish the brain-wide direct inputs of two major types of striatal interneurons and allude to distinct roles in regulating striatal activity and controlling behavior.
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spelling pubmed-59299092018-05-03 Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions Klug, Jason R Engelhardt, Max D Cadman, Cara N Li, Hao Smith, Jared B Ayala, Sarah Williams, Elora W Hoffman, Hilary Jin, Xin eLife Neuroscience Striatal cholinergic (ChAT) and parvalbumin (PV) interneurons exert powerful influences on striatal function in health and disease, yet little is known about the organization of their inputs. Here using rabies tracing, electrophysiology and genetic tools, we compare the whole-brain inputs to these two types of striatal interneurons and dissect their functional connectivity in mice. ChAT interneurons receive a substantial cortical input from associative regions of cortex, such as the orbitofrontal cortex. Amongst subcortical inputs, a previously unknown inhibitory thalamic reticular nucleus input to striatal PV interneurons is identified. Additionally, the external segment of the globus pallidus targets striatal ChAT interneurons, which is sufficient to inhibit tonic ChAT interneuron firing. Finally, we describe a novel excitatory pathway from the pedunculopontine nucleus that innervates ChAT interneurons. These results establish the brain-wide direct inputs of two major types of striatal interneurons and allude to distinct roles in regulating striatal activity and controlling behavior. eLife Sciences Publications, Ltd 2018-05-01 /pmc/articles/PMC5929909/ /pubmed/29714166 http://dx.doi.org/10.7554/eLife.35657 Text en © 2018, Klug et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Klug, Jason R
Engelhardt, Max D
Cadman, Cara N
Li, Hao
Smith, Jared B
Ayala, Sarah
Williams, Elora W
Hoffman, Hilary
Jin, Xin
Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions
title Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions
title_full Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions
title_fullStr Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions
title_full_unstemmed Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions
title_short Differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions
title_sort differential inputs to striatal cholinergic and parvalbumin interneurons imply functional distinctions
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5929909/
https://www.ncbi.nlm.nih.gov/pubmed/29714166
http://dx.doi.org/10.7554/eLife.35657
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