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Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum

The medial prefrontal cortex (mPFC) steers goal-directed actions and withholds inappropriate behavior. Dorsal and ventral mPFC (dmPFC/vmPFC) circuits have distinct roles in cognitive control, but underlying mechanisms are poorly understood. Here we use neuroanatomical tracing techniques, in vitro el...

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Autores principales: de Kloet, Sybren F., Bruinsma, Bastiaan, Terra, Huub, Heistek, Tim S., Passchier, Emma M. J., van den Berg, Alexandra R., Luchicchi, Antonio, Min, Rogier, Pattij, Tommy, Mansvelder, Huibert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012364/
https://www.ncbi.nlm.nih.gov/pubmed/33790281
http://dx.doi.org/10.1038/s41467-021-22260-7
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author de Kloet, Sybren F.
Bruinsma, Bastiaan
Terra, Huub
Heistek, Tim S.
Passchier, Emma M. J.
van den Berg, Alexandra R.
Luchicchi, Antonio
Min, Rogier
Pattij, Tommy
Mansvelder, Huibert D.
author_facet de Kloet, Sybren F.
Bruinsma, Bastiaan
Terra, Huub
Heistek, Tim S.
Passchier, Emma M. J.
van den Berg, Alexandra R.
Luchicchi, Antonio
Min, Rogier
Pattij, Tommy
Mansvelder, Huibert D.
author_sort de Kloet, Sybren F.
collection PubMed
description The medial prefrontal cortex (mPFC) steers goal-directed actions and withholds inappropriate behavior. Dorsal and ventral mPFC (dmPFC/vmPFC) circuits have distinct roles in cognitive control, but underlying mechanisms are poorly understood. Here we use neuroanatomical tracing techniques, in vitro electrophysiology, chemogenetics and fiber photometry in rats engaged in a 5-choice serial reaction time task to characterize dmPFC and vmPFC outputs to distinct thalamic and striatal subdomains. We identify four spatially segregated projection neuron populations in the mPFC. Using fiber photometry we show that these projections distinctly encode behavior. Postsynaptic striatal and thalamic neurons differentially process synaptic inputs from dmPFC and vmPFC, highlighting mechanisms that potentially amplify distinct pathways underlying cognitive control of behavior. Chemogenetic silencing of dmPFC and vmPFC projections to lateral and medial mediodorsal thalamus subregions oppositely regulate cognitive control. In addition, dmPFC neurons projecting to striatum and thalamus divergently regulate cognitive control. Collectively, we show that mPFC output pathways targeting anatomically and functionally distinct striatal and thalamic subregions encode bi-directional command of cognitive control.
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spelling pubmed-80123642021-04-16 Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum de Kloet, Sybren F. Bruinsma, Bastiaan Terra, Huub Heistek, Tim S. Passchier, Emma M. J. van den Berg, Alexandra R. Luchicchi, Antonio Min, Rogier Pattij, Tommy Mansvelder, Huibert D. Nat Commun Article The medial prefrontal cortex (mPFC) steers goal-directed actions and withholds inappropriate behavior. Dorsal and ventral mPFC (dmPFC/vmPFC) circuits have distinct roles in cognitive control, but underlying mechanisms are poorly understood. Here we use neuroanatomical tracing techniques, in vitro electrophysiology, chemogenetics and fiber photometry in rats engaged in a 5-choice serial reaction time task to characterize dmPFC and vmPFC outputs to distinct thalamic and striatal subdomains. We identify four spatially segregated projection neuron populations in the mPFC. Using fiber photometry we show that these projections distinctly encode behavior. Postsynaptic striatal and thalamic neurons differentially process synaptic inputs from dmPFC and vmPFC, highlighting mechanisms that potentially amplify distinct pathways underlying cognitive control of behavior. Chemogenetic silencing of dmPFC and vmPFC projections to lateral and medial mediodorsal thalamus subregions oppositely regulate cognitive control. In addition, dmPFC neurons projecting to striatum and thalamus divergently regulate cognitive control. Collectively, we show that mPFC output pathways targeting anatomically and functionally distinct striatal and thalamic subregions encode bi-directional command of cognitive control. Nature Publishing Group UK 2021-03-31 /pmc/articles/PMC8012364/ /pubmed/33790281 http://dx.doi.org/10.1038/s41467-021-22260-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
de Kloet, Sybren F.
Bruinsma, Bastiaan
Terra, Huub
Heistek, Tim S.
Passchier, Emma M. J.
van den Berg, Alexandra R.
Luchicchi, Antonio
Min, Rogier
Pattij, Tommy
Mansvelder, Huibert D.
Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum
title Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum
title_full Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum
title_fullStr Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum
title_full_unstemmed Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum
title_short Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum
title_sort bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012364/
https://www.ncbi.nlm.nih.gov/pubmed/33790281
http://dx.doi.org/10.1038/s41467-021-22260-7
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