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Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons

A substantial proportion of raphe neurons are glutamatergic. However, little is known about how these glutamatergic neurons modulate the forebrain. We investigated how glutamatergic median raphe nucleus (MRN) input modulates the medial prefrontal cortex (mPFC), a critical component of fear circuitry...

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Autores principales: Collins, Stuart A., Stinson, Hannah E., Himes, Amanda, Nestor-Kalinoski, Andrea, Ninan, Ipe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637752/
https://www.ncbi.nlm.nih.gov/pubmed/37948526
http://dx.doi.org/10.1126/sciadv.adg4800
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author Collins, Stuart A.
Stinson, Hannah E.
Himes, Amanda
Nestor-Kalinoski, Andrea
Ninan, Ipe
author_facet Collins, Stuart A.
Stinson, Hannah E.
Himes, Amanda
Nestor-Kalinoski, Andrea
Ninan, Ipe
author_sort Collins, Stuart A.
collection PubMed
description A substantial proportion of raphe neurons are glutamatergic. However, little is known about how these glutamatergic neurons modulate the forebrain. We investigated how glutamatergic median raphe nucleus (MRN) input modulates the medial prefrontal cortex (mPFC), a critical component of fear circuitry. We show that vesicular glutamate transporter 3 (VGLUT3)–expressing MRN neurons activate VGLUT3- and somatostatin-expressing neurons in the mPFC. Consistent with this modulation of mPFC GABAergic neurons, activation of MRN (VGLUT3) neurons enhances GABAergic transmission in mPFC pyramidal neurons and attenuates fear memory in female but not male mice. Serotonin plays a key role in MRN (VGLUT3) neuron–mediated GABAergic plasticity in the mPFC. In agreement with these female-specific effects, we observed sex differences in glutamatergic transmission onto MRN (VGLUT3) neurons and in mPFC (VGLUT3) neuron–mediated dual release of glutamate and GABA. Our results demonstrate a cell type–specific modulation of the mPFC by MRN (VGLUT3) neurons and reveal a sex-specific role of this neuromodulation in mPFC synaptic plasticity.
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spelling pubmed-106377522023-11-11 Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons Collins, Stuart A. Stinson, Hannah E. Himes, Amanda Nestor-Kalinoski, Andrea Ninan, Ipe Sci Adv Neuroscience A substantial proportion of raphe neurons are glutamatergic. However, little is known about how these glutamatergic neurons modulate the forebrain. We investigated how glutamatergic median raphe nucleus (MRN) input modulates the medial prefrontal cortex (mPFC), a critical component of fear circuitry. We show that vesicular glutamate transporter 3 (VGLUT3)–expressing MRN neurons activate VGLUT3- and somatostatin-expressing neurons in the mPFC. Consistent with this modulation of mPFC GABAergic neurons, activation of MRN (VGLUT3) neurons enhances GABAergic transmission in mPFC pyramidal neurons and attenuates fear memory in female but not male mice. Serotonin plays a key role in MRN (VGLUT3) neuron–mediated GABAergic plasticity in the mPFC. In agreement with these female-specific effects, we observed sex differences in glutamatergic transmission onto MRN (VGLUT3) neurons and in mPFC (VGLUT3) neuron–mediated dual release of glutamate and GABA. Our results demonstrate a cell type–specific modulation of the mPFC by MRN (VGLUT3) neurons and reveal a sex-specific role of this neuromodulation in mPFC synaptic plasticity. American Association for the Advancement of Science 2023-11-10 /pmc/articles/PMC10637752/ /pubmed/37948526 http://dx.doi.org/10.1126/sciadv.adg4800 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Neuroscience
Collins, Stuart A.
Stinson, Hannah E.
Himes, Amanda
Nestor-Kalinoski, Andrea
Ninan, Ipe
Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons
title Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons
title_full Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons
title_fullStr Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons
title_full_unstemmed Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons
title_short Sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons
title_sort sex-specific modulation of the medial prefrontal cortex by glutamatergic median raphe neurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637752/
https://www.ncbi.nlm.nih.gov/pubmed/37948526
http://dx.doi.org/10.1126/sciadv.adg4800
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