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Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex

The medial prefrontal cortex (mPFC) integrates inputs from multiple subcortical regions including the mediodorsal nucleus of the thalamus (MD) and the ventral hippocampus (vHPC). How the mPFC differentially processes these inputs is not known. One possibility is that these two inputs target discreet...

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Autores principales: Canetta, Sarah, Teboul, Eric, Holt, Emma, Bolkan, Scott S, Padilla-Coreano, Nancy, Gordon, Joshua A, Harrison, Neil L, Kellendonk, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750130/
https://www.ncbi.nlm.nih.gov/pubmed/33381761
http://dx.doi.org/10.1093/texcom/tgaa084
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author Canetta, Sarah
Teboul, Eric
Holt, Emma
Bolkan, Scott S
Padilla-Coreano, Nancy
Gordon, Joshua A
Harrison, Neil L
Kellendonk, Christoph
author_facet Canetta, Sarah
Teboul, Eric
Holt, Emma
Bolkan, Scott S
Padilla-Coreano, Nancy
Gordon, Joshua A
Harrison, Neil L
Kellendonk, Christoph
author_sort Canetta, Sarah
collection PubMed
description The medial prefrontal cortex (mPFC) integrates inputs from multiple subcortical regions including the mediodorsal nucleus of the thalamus (MD) and the ventral hippocampus (vHPC). How the mPFC differentially processes these inputs is not known. One possibility is that these two inputs target discreet populations of mPFC cells. Alternatively, individual prefrontal cells could receive convergent inputs but distinguish between both inputs based on synaptic differences, such as communication frequency. To address this, we utilized a dual wavelength optogenetic approach to stimulate MD and vHPC inputs onto single, genetically defined mPFC neuronal subtypes. Specifically, we compared the convergence and synaptic dynamics of both inputs onto mPFC pyramidal cells, and parvalbumin (PV)- and vasoactive intestinal peptide (VIP)-expressing interneurons. We found that all individual pyramidal neurons in layer 2/3 of the mPFC receive convergent input from both MD and vHPC. In contrast, PV neurons receive input biased from the MD, while VIP cells receive input biased from the vHPC. Independent of the target, MD inputs transferred information more reliably at higher frequencies (20 Hz) than vHPC inputs. Thus, MD and vHPC projections converge functionally onto mPFC pyramidal cells, but both inputs are distinguished by frequency-dependent synaptic dynamics and preferential engagement of discreet interneuron populations.
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spelling pubmed-77501302020-12-28 Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex Canetta, Sarah Teboul, Eric Holt, Emma Bolkan, Scott S Padilla-Coreano, Nancy Gordon, Joshua A Harrison, Neil L Kellendonk, Christoph Cereb Cortex Commun Original Article The medial prefrontal cortex (mPFC) integrates inputs from multiple subcortical regions including the mediodorsal nucleus of the thalamus (MD) and the ventral hippocampus (vHPC). How the mPFC differentially processes these inputs is not known. One possibility is that these two inputs target discreet populations of mPFC cells. Alternatively, individual prefrontal cells could receive convergent inputs but distinguish between both inputs based on synaptic differences, such as communication frequency. To address this, we utilized a dual wavelength optogenetic approach to stimulate MD and vHPC inputs onto single, genetically defined mPFC neuronal subtypes. Specifically, we compared the convergence and synaptic dynamics of both inputs onto mPFC pyramidal cells, and parvalbumin (PV)- and vasoactive intestinal peptide (VIP)-expressing interneurons. We found that all individual pyramidal neurons in layer 2/3 of the mPFC receive convergent input from both MD and vHPC. In contrast, PV neurons receive input biased from the MD, while VIP cells receive input biased from the vHPC. Independent of the target, MD inputs transferred information more reliably at higher frequencies (20 Hz) than vHPC inputs. Thus, MD and vHPC projections converge functionally onto mPFC pyramidal cells, but both inputs are distinguished by frequency-dependent synaptic dynamics and preferential engagement of discreet interneuron populations. Oxford University Press 2020-11-06 /pmc/articles/PMC7750130/ /pubmed/33381761 http://dx.doi.org/10.1093/texcom/tgaa084 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Canetta, Sarah
Teboul, Eric
Holt, Emma
Bolkan, Scott S
Padilla-Coreano, Nancy
Gordon, Joshua A
Harrison, Neil L
Kellendonk, Christoph
Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex
title Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex
title_full Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex
title_fullStr Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex
title_full_unstemmed Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex
title_short Differential Synaptic Dynamics and Circuit Connectivity of Hippocampal and Thalamic Inputs to the Prefrontal Cortex
title_sort differential synaptic dynamics and circuit connectivity of hippocampal and thalamic inputs to the prefrontal cortex
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750130/
https://www.ncbi.nlm.nih.gov/pubmed/33381761
http://dx.doi.org/10.1093/texcom/tgaa084
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