GluN3A excitatory glycine receptors control adult cortical and amygdalar circuits
GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the forma...
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Published in | Neuron (Cambridge, Mass.) Vol. 110; no. 15; pp. 2438 - 2454.e8 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
03.08.2022
Elsevier Cell Press |
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Abstract | GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs) and their tonic activation by extracellular glycine. eGlyRs are mostly extrasynaptic and reside in specific neuronal populations, including the principal cells of the basolateral amygdala (BLA) and SST-positive interneurons (SST-INs) of the neocortex. In the BLA, tonic eGlyR currents are sensitive to fear-conditioning protocols, are subject to neuromodulation by the dopaminergic system, and control the stability of fear memories. In the neocortex, eGlyRs control the in vivo spiking of SST-INs and the behavior-dependent modulation of cortical activity. GluN3A-containing eGlyRs thus represent a novel and widespread signaling modality in the adult brain, with attributes that strikingly depart from those of conventional NMDARs.
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•In mice, GluN3A is expressed by SST-INs in the cortex and pyramidal neurons in the BLA•GluN3A assembles as excitatory glycine GluN1/GluN3A receptors (eGlyRs)•eGlyRs detect extracellular glycine levels and generate tonic excitatory currents•eGlyRs tune the function of SST-INs in cortex and alter the formation of fear memories in BLA
Bossi et al. show that GluN3A subunits control the activity of selective neuronal populations in the adult mouse brain via the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs). Functional analysis reveals that eGlyRs regulate the recruitment of somatostatin-positive interneurons in the neocortex and participate in the stability of fear memories in the BLA. |
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AbstractList | GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs) and their tonic activation by extracellular glycine. eGlyRs are mostly extrasy- naptic and reside in specific neuronal populations, including the principal cells of the basolateral amygdala (BLA) and SST-positive interneurons (SST-INs) of the neocortex. In the BLA, tonic eGlyR currents are sensitive to fear-conditioning protocols, are subject to neuromodulation by the dopaminergic system, and control the sta- bility of fear memories. In the neocortex, eGlyRs control the in vivo spiking of SST-INs and the behavior-depen- dent modulation of cortical activity. GluN3A-containing eGlyRs thus represent a novel and widespread signaling modality in the adult brain, with attributes that strikingly depart from those of conventional NMDARs. GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs) and their tonic activation by extracellular glycine. eGlyRs are mostly extrasynaptic and reside in specific neuronal populations, including the principal cells of the basolateral amygdala (BLA) and SST-positive interneurons (SST-INs) of the neocortex. In the BLA, tonic eGlyR currents are sensitive to fear-conditioning protocols, are subject to neuromodulation by the dopaminergic system, and control the stability of fear memories. In the neocortex, eGlyRs control the in vivo spiking of SST-INs and the behavior-dependent modulation of cortical activity. GluN3A-containing eGlyRs thus represent a novel and widespread signaling modality in the adult brain, with attributes that strikingly depart from those of conventional NMDARs. GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs) and their tonic activation by extracellular glycine. eGlyRs are mostly extrasynaptic and reside in specific neuronal populations, including the principal cells of the basolateral amygdala (BLA) and SST-positive interneurons (SST-INs) of the neocortex. In the BLA, tonic eGlyR currents are sensitive to fear-conditioning protocols, are subject to neuromodulation by the dopaminergic system, and control the stability of fear memories. In the neocortex, eGlyRs control the in vivo spiking of SST-INs and the behavior-dependent modulation of cortical activity. GluN3A-containing eGlyRs thus represent a novel and widespread signaling modality in the adult brain, with attributes that strikingly depart from those of conventional NMDARs.GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs) and their tonic activation by extracellular glycine. eGlyRs are mostly extrasynaptic and reside in specific neuronal populations, including the principal cells of the basolateral amygdala (BLA) and SST-positive interneurons (SST-INs) of the neocortex. In the BLA, tonic eGlyR currents are sensitive to fear-conditioning protocols, are subject to neuromodulation by the dopaminergic system, and control the stability of fear memories. In the neocortex, eGlyRs control the in vivo spiking of SST-INs and the behavior-dependent modulation of cortical activity. GluN3A-containing eGlyRs thus represent a novel and widespread signaling modality in the adult brain, with attributes that strikingly depart from those of conventional NMDARs. GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs) and their tonic activation by extracellular glycine. eGlyRs are mostly extrasynaptic and reside in specific neuronal populations, including the principal cells of the basolateral amygdala (BLA) and SST-positive interneurons (SST-INs) of the neocortex. In the BLA, tonic eGlyR currents are sensitive to fear-conditioning protocols, are subject to neuromodulation by the dopaminergic system, and control the stability of fear memories. In the neocortex, eGlyRs control the in vivo spiking of SST-INs and the behavior-dependent modulation of cortical activity. GluN3A-containing eGlyRs thus represent a novel and widespread signaling modality in the adult brain, with attributes that strikingly depart from those of conventional NMDARs. • In mice, GluN3A is expressed by SST-INs in the cortex and pyramidal neurons in the BLA • GluN3A assembles as excitatory glycine GluN1/GluN3A receptors (eGlyRs) • eGlyRs detect extracellular glycine levels and generate tonic excitatory currents • eGlyRs tune the function of SST-INs in cortex and alter the formation of fear memories in BLA Bossi et al. show that GluN3A subunits control the activity of selective neuronal populations in the adult mouse brain via the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs). Functional analysis reveals that eGlyRs regulate the recruitment of somatostatin-positive interneurons in the neocortex and participate in the stability of fear memories in the BLA. GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of GluN3A subunits controls the excitability of mouse adult cortical and amygdalar circuits via an unusual signaling mechanism involving the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs) and their tonic activation by extracellular glycine. eGlyRs are mostly extrasynaptic and reside in specific neuronal populations, including the principal cells of the basolateral amygdala (BLA) and SST-positive interneurons (SST-INs) of the neocortex. In the BLA, tonic eGlyR currents are sensitive to fear-conditioning protocols, are subject to neuromodulation by the dopaminergic system, and control the stability of fear memories. In the neocortex, eGlyRs control the in vivo spiking of SST-INs and the behavior-dependent modulation of cortical activity. GluN3A-containing eGlyRs thus represent a novel and widespread signaling modality in the adult brain, with attributes that strikingly depart from those of conventional NMDARs. [Display omitted] •In mice, GluN3A is expressed by SST-INs in the cortex and pyramidal neurons in the BLA•GluN3A assembles as excitatory glycine GluN1/GluN3A receptors (eGlyRs)•eGlyRs detect extracellular glycine levels and generate tonic excitatory currents•eGlyRs tune the function of SST-INs in cortex and alter the formation of fear memories in BLA Bossi et al. show that GluN3A subunits control the activity of selective neuronal populations in the adult mouse brain via the formation of excitatory glycine GluN1/GluN3A receptors (eGlyRs). Functional analysis reveals that eGlyRs regulate the recruitment of somatostatin-positive interneurons in the neocortex and participate in the stability of fear memories in the BLA. |
Author | Lourenço, Joana Rebola, Nelson de Brito Van Velze, Marcel Ellis-Davies, Graham C.R. Dhanasobhon, Dhanasak Frontera, Jimena Popa, Daniela Paoletti, Pierre Murillo, Alvaro Bacci, Alberto Luján, Rafael Casado, Mariano Perez-Otaño, Isabel Bossi, Simon |
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Keywords | cortex tonic activation amygdala neurotransmission receptors glycine somatostatin interneurons NMDA interneuron GluN3A fear |
Language | English |
License | This is an open access article under the CC BY-NC-ND license. Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved. Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0 This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 PMCID: PMC9365314 Present address: UK Dementia Research Institute at Cardiff University, CF24 4HQ Cardiff, UK These authors contributed equally Senior author Lead contact |
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Snippet | GluN3A is an atypical glycine-binding subunit of NMDA receptors (NMDARs) whose actions in the brain are mostly unknown. Here, we show that the expression of... |
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SubjectTerms | amygdala cortex fear GluN3A glycine interneuron Life Sciences Neurobiology Neurons and Cognition neurotransmission NMDA receptors somatostatin interneurons tonic activation |
Title | GluN3A excitatory glycine receptors control adult cortical and amygdalar circuits |
URI | https://dx.doi.org/10.1016/j.neuron.2022.05.016 https://www.ncbi.nlm.nih.gov/pubmed/35700736 https://www.proquest.com/docview/2676925219 https://hal.science/hal-03782718 https://pubmed.ncbi.nlm.nih.gov/PMC9365314 |
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