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...

Full description

Saved in:
Bibliographic Details
Published inNeuron (Cambridge, Mass.) Vol. 110; no. 15; pp. 2438 - 2454.e8
Main Authors Bossi, Simon, Dhanasobhon, Dhanasak, Ellis-Davies, Graham C.R., Frontera, Jimena, de Brito Van Velze, Marcel, Lourenço, Joana, Murillo, Alvaro, Luján, Rafael, Casado, Mariano, Perez-Otaño, Isabel, Bacci, Alberto, Popa, Daniela, Paoletti, Pierre, Rebola, Nelson
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 03.08.2022
Elsevier
Cell Press
Subjects
Online AccessGet full text

Cover

Loading…
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. [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.
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
Author_xml – sequence: 1
  givenname: Simon
  surname: Bossi
  fullname: Bossi, Simon
  organization: Institut de Biologie de l’Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France
– sequence: 2
  givenname: Dhanasak
  surname: Dhanasobhon
  fullname: Dhanasobhon, Dhanasak
  organization: Sorbonne Université, Institut Du Cerveau-Paris Brain Institute-ICM, Inserm U1127, CNRS UMR 7225, 47 Boulevard de l’Hôpital, 75013 Paris, France
– sequence: 3
  givenname: Graham C.R.
  surname: Ellis-Davies
  fullname: Ellis-Davies, Graham C.R.
  organization: Department of Neuroscience, Mount Sinai School of Medicine, One Gustave Levy Place, New York, NY 10029, USA
– sequence: 4
  givenname: Jimena
  surname: Frontera
  fullname: Frontera, Jimena
  organization: Institut de Biologie de l’Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France
– sequence: 5
  givenname: Marcel
  surname: de Brito Van Velze
  fullname: de Brito Van Velze, Marcel
  organization: Sorbonne Université, Institut Du Cerveau-Paris Brain Institute-ICM, Inserm U1127, CNRS UMR 7225, 47 Boulevard de l’Hôpital, 75013 Paris, France
– sequence: 6
  givenname: Joana
  surname: Lourenço
  fullname: Lourenço, Joana
  organization: Sorbonne Université, Institut Du Cerveau-Paris Brain Institute-ICM, Inserm U1127, CNRS UMR 7225, 47 Boulevard de l’Hôpital, 75013 Paris, France
– sequence: 7
  givenname: Alvaro
  surname: Murillo
  fullname: Murillo, Alvaro
  organization: Instituto de Neurociencias (CSIC-UMH), San Juan de Alicante 03550, Spain
– sequence: 8
  givenname: Rafael
  surname: Luján
  fullname: Luján, Rafael
  organization: Synaptic Structure Laboratory, Instituto de Investigación en Discapacidades Neurológicas (IDINE), Facultad de Medicina, Universidad Castilla-La Mancha, 02006 Albacete, Spain
– sequence: 9
  givenname: Mariano
  surname: Casado
  fullname: Casado, Mariano
  organization: Institut de Biologie de l’Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France
– sequence: 10
  givenname: Isabel
  surname: Perez-Otaño
  fullname: Perez-Otaño, Isabel
  organization: Instituto de Neurociencias (CSIC-UMH), San Juan de Alicante 03550, Spain
– sequence: 11
  givenname: Alberto
  surname: Bacci
  fullname: Bacci, Alberto
  organization: Sorbonne Université, Institut Du Cerveau-Paris Brain Institute-ICM, Inserm U1127, CNRS UMR 7225, 47 Boulevard de l’Hôpital, 75013 Paris, France
– sequence: 12
  givenname: Daniela
  surname: Popa
  fullname: Popa, Daniela
  organization: Institut de Biologie de l’Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France
– sequence: 13
  givenname: Pierre
  surname: Paoletti
  fullname: Paoletti, Pierre
  email: pierre.paoletti@ens.psl.eu
  organization: Institut de Biologie de l’Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France
– sequence: 14
  givenname: Nelson
  surname: Rebola
  fullname: Rebola, Nelson
  email: nelson.rebola@icm-institute.org
  organization: Sorbonne Université, Institut Du Cerveau-Paris Brain Institute-ICM, Inserm U1127, CNRS UMR 7225, 47 Boulevard de l’Hôpital, 75013 Paris, France
BackLink https://www.ncbi.nlm.nih.gov/pubmed/35700736$$D View this record in MEDLINE/PubMed
https://hal.science/hal-03782718$$DView record in HAL
BookMark eNpdUU1vEzEQtVARTQv_AKE9wmEXf60dX5CiirZIEQgJzpbXnk0dOXawdyPy73GUlq_TaN7MvHl67wpdxBQBodcEdwQT8X7bRZhzih3FlHa47yr4DC0IVrLlRKkLtMBLJVpBJbtEV6VsMSa8V-QFumS9xFgysUBf78L8ma0a-Gn9ZKaUj80mHK2P0GSwsK9IaWyKU06hMW4OU-3y5K2pbXSN2R03zgSTG-uznf1UXqLnowkFXj3Wa_T99uO3m_t2_eXu081q3QIXcmrNaEZhOGbOEiwdN5IKDsLiQfR4cFwp2Q8jUGDEMjmKpaMjh2F0gxBMWcyu0Ycz734eduAsVI0m6H32O5OPOhmv_51E_6A36aAVEz0jvBK8OxM8_Hd2v1rrE4aZXFJJlgdSd98-Psvpxwxl0jtfLIRgIqS5aCqkULSnRNXVN3_r-s385Pkf4VDdOXjIulgP0YLz1fJJu-Q1wfoUst7qc8j6FLLGva4g-wXH4555
ContentType Journal Article
Copyright 2022 The Authors
Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.
Distributed under a Creative Commons Attribution 4.0 International License
2022 The Authors 2022
Copyright_xml – notice: 2022 The Authors
– notice: Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.
– notice: Distributed under a Creative Commons Attribution 4.0 International License
– notice: 2022 The Authors 2022
DBID 6I.
AAFTH
NPM
7X8
1XC
VOOES
5PM
DOI 10.1016/j.neuron.2022.05.016
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
PubMed
MEDLINE - Academic
Hyper Article en Ligne (HAL)
Hyper Article en Ligne (HAL) (Open Access)
PubMed Central (Full Participant titles)
DatabaseTitle PubMed
MEDLINE - Academic
DatabaseTitleList
PubMed
MEDLINE - Academic


Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
Biology
EISSN 1097-4199
EndPage 2454.e8
ExternalDocumentID PMC9365314
oai_HAL_hal_03782718v1
35700736
S0896627322004573
Genre Journal Article
GroupedDBID ---
--K
-DZ
-~X
0R~
123
1RT
1~5
26-
2WC
4.4
457
4G.
53G
5RE
62-
6I.
7-5
8C1
8FE
8FH
AACTN
AAEDW
AAFTH
AAIAV
AAKRW
AAKUH
AALRI
AAUCE
AAVLU
AAXUO
ABJNI
ABMAC
ABMWF
ABVKL
ACGFO
ACGFS
ACIWK
ACNCT
ACPRK
ADBBV
ADEZE
ADFRT
ADJPV
AEFWE
AENEX
AEXQZ
AFTJW
AGKMS
AHHHB
AHMBA
AITUG
ALKID
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
AQUVI
ASPBG
AVWKF
AZFZN
BAWUL
BKEYQ
BKNYI
BPHCQ
BVXVI
CS3
DIK
DU5
E3Z
EBS
F5P
FCP
FDB
FEDTE
FIRID
HVGLF
IAO
IHE
IHR
INH
IXB
J1W
JIG
K-O
KQ8
L7B
LK8
LX5
M2O
M3Z
M41
N9A
O-L
O9-
OK1
P2P
P6G
PQQKQ
PROAC
RCE
ROL
RPZ
SCP
SDP
SES
SSZ
TR2
WOW
WQ6
ZA5
AAEDT
AAMRU
ADVLN
AKAPO
AKRWK
NPM
7X8
AAFWJ
AAYWO
ABDGV
ACVFH
ADCNI
AEUPX
AFPUW
AGCQF
AIGII
AKBMS
AKYEP
APXCP
.55
.GJ
1XC
29N
3O-
5VS
AAIKJ
AAQFI
AAQXK
ABWVN
ACRPL
ADMUD
ADNMO
AGHFR
AGQPQ
EJD
FGOYB
G-2
HZ~
ITC
MVM
OZT
R2-
RIG
VOOES
X7M
ZGI
ZKB
5PM
EFKBS
ID FETCH-LOGICAL-e467t-afaf6a403dc107d4a7264e6c0b650bd49975bfe2e31c37f68d2f4ebfdb6639c03
IEDL.DBID IXB
ISSN 0896-6273
1097-4199
IngestDate Thu Aug 21 17:56:26 EDT 2025
Fri May 09 12:22:51 EDT 2025
Fri Jul 11 09:18:02 EDT 2025
Thu Apr 03 07:04:29 EDT 2025
Fri Feb 23 02:39:39 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 15
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/).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-e467t-afaf6a403dc107d4a7264e6c0b650bd49975bfe2e31c37f68d2f4ebfdb6639c03
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
ORCID 0000-0002-8389-1122
0000-0002-9975-4747
0000-0001-5550-9291
OpenAccessLink https://www.sciencedirect.com/science/article/pii/S0896627322004573
PMID 35700736
PQID 2676925219
PQPubID 23479
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_9365314
hal_primary_oai_HAL_hal_03782718v1
proquest_miscellaneous_2676925219
pubmed_primary_35700736
elsevier_sciencedirect_doi_10_1016_j_neuron_2022_05_016
PublicationCentury 2000
PublicationDate 2022-08-03
PublicationDateYYYYMMDD 2022-08-03
PublicationDate_xml – month: 08
  year: 2022
  text: 2022-08-03
  day: 03
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Neuron (Cambridge, Mass.)
PublicationTitleAlternate Neuron
PublicationYear 2022
Publisher Elsevier Inc
Elsevier
Cell Press
Publisher_xml – name: Elsevier Inc
– name: Elsevier
– name: Cell Press
References Harvey, Yee (bib16) 2013; 12
Favuzzi, Deogracias, Marques-Smith, Maeso, Jezequel, Exposito-Alonso, Balia, Kroon, Hinojosa, Maraver, Rico (bib11) 2019; 363
Ellis-Davies (bib10) 2011; 6
Pérez-Otaño, Larsen, Wesseling (bib46) 2016; 17
Perez-Otano, Schulteis, Contractor, Lipton, Trimmer, Sucher, Heinemann (bib48) 2001; 21
Oh, Harris, Ng, Winslow, Cain, Mihalas, Wang, Lau, Kuan, Henry (bib37) 2014; 508
Corrie, Kaplan, Forbush, Ogden, Trentham (bib6) 2016; 15
Rhomberg, Rovira-Esteban, Vikór, Paradiso, Kremser, Nagy-Pál, Papp, Tasan, Erdélyi, Szabó (bib53) 2018; 38
Lodge, Mercier (bib23) 2015; 172
Traynelis, Wollmuth, McBain, Menniti, Vance, Ogden, Hansen, Yuan, Myers, Dingledine (bib68) 2010; 62
Marco, Murillo, Pérez-Otaño (bib26) 2018; 26
Al-Hallaq, Jarabek, Fu, Vicini, Wolfe, Yasuda (bib1) 2002; 62
Ulbrich, Isacoff (bib69) 2008; 105
Pachitariu, Stringer, Dipoppa, Schröder, Rossi, Dalgleish, Carandini, Harris (bib39) 2017
Westergren, Nyström, Hamberger, Nordborg, Johansson (bib71) 1994; 62
Nicoll (bib79) 2017; 93
Awobuluyi, Yang, Ye, Chatterton, Godzik, Lipton, Zhang (bib2) 2007; 71
Crawley, Conde-Dusman, Pérez-Otaño (bib7) 2022; 600
Papageorgiou, Corrie (bib43) 2000; 56
Yao, Mayer (bib73) 2006; 26
Hodge, Bakken, Miller, Smith, Barkan, Graybuck, Close, Long, Johansen, Penn (bib17) 2019; 573
Johnson, Ascher (bib20) 1987; 325
McGinley, Vinck, Reimer, Batista-Brito, Zagha, Cadwell, Tolias, Cardin, McCormick (bib29) 2015; 87
Yaeger, Ringach, Trachtenberg (bib72) 2019; 567
Wang, Tu, Bonet, Aubrey, Supplisson (bib70) 2013; 80
Das, Sasaki, Rothe, Premkumar, Takasu, Crandall, Dikkes, Conner, Rayudu, Cheung (bib8) 1998; 393
Pala, Petersen (bib41) 2015; 85
Pakan, Lowe, Dylda, Keemink, Currie, Coutts, Rochefort (bib40) 2016; 5
Stringer, Pachitariu, Steinmetz, Carandini, Harris (bib62) 2019; 571
Rothman, Silver (bib56) 2018; 12
Sakimura, Kutsuwada, Ito, Manabe, Takayama, Kushiya, Yagi, Aizawa, Inoue, Sugiyama (bib57) 1995; 373
Johansen, Cain, Ostroff, LeDoux (bib19) 2011; 147
Reimer, Froudarakis, Cadwell, Yatsenko, Denfield, Tolias (bib52) 2014; 84
Pfeffer, Xue, He, Huang, Scanziani (bib49) 2013; 16
Zeilhofer, Studler, Arabadzisz, Schweizer, Ahmadi, Layh, Bösl, Fritschy (bib75) 2005; 482
Muñoz, Tremblay, Levenstein, Rudy (bib33) 2017; 355
Tong, Takahashi, Tu, Shin, Talantova, Zago, Xia, Nie, Goetz, Zhang (bib67) 2008; 99
Basu, Tsai, Ma, Ehmsen, Mustafa, Han, Jiang, Benneyworth, Froimowitz, Lange (bib3) 2009; 14
Chatterton, Awobuluyi, Premkumar, Takahashi, Talantova, Shin, Cui, Tu, Sevarino, Nakanishi (bib4) 2002; 415
Ciabarra, Sevarino, Gahn, Pecht, Heinemann, Sevarino (bib5) 1995; 15
Saleem, Ayaz, Jeffery, Harris, Carandini (bib58) 2013; 16
Marco, Giralt, Petrovic, Pouladi, Martínez-Turrillas, Martínez-Hernández, Kaltenbach, Torres-Peraza, Graham, Watanabe (bib25) 2013; 19
Sucher, Akbarian, Chi, Leclerc, Awobuluyi, Deitcher, Wu, Yuan, Jones, Lipton (bib65) 1995; 15
Poulet, Petersen (bib51) 2008; 454
Rothman, Cathala, Steuber, Silver (bib55) 2009; 457
Gentet, Kremer, Taniguchi, Huang, Staiger, Petersen (bib13) 2012; 15
Madry, Mesic, Bartholomäus, Nicke, Betz, Laube (bib24) 2007; 354
Matsuzaki, Hayama, Kasai, Ellis-Davies (bib27) 2010; 6
Dipoppa, Ranson, Krumin, Pachitariu, Carandini, Harris (bib9) 2018; 98
Legendre (bib78) 2001
Paoletti, Bellone, Zhou (bib42) 2013; 14
Stroebel, Mony, Paoletti (bib64) 2021; 193
Ferreira, Papouin, Ladépêche, Yao, Langlais, Bouchet, Dulong, Mothet, Sacchi, Pollegioni (bib12) 2017; 6
Pfisterer, Petukhov, Demharter, Meichsner, Thompson, Batiuk, Asenjo-Martinez, Vasistha, Thakur, Mikkelsen (bib50) 2020; 11
Mothet, Parent, Wolosker, Brady, Linden, Ferris, Rogawski, Snyder (bib30) 2000; 97
Yuan, Mameli, O’Connor, Dey, Verpelli, Sala, Perez-Otano, Lüscher, Bellone (bib74) 2013; 80
Mueller, Meador-Woodruff (bib31) 2004; 71
Zhang, Herde, Mitchell, Whitfield, Wulff, Vongsouthi, Sanchez-Romero, Gulakova, Minge, Breithausen (bib76) 2018; 14
Sheng, Kim (bib60) 2011; 3
Zhu, Yi, Epplin, Liu, Summer, Mizu, Shaulsky, Xiangwei, Tang, Burger (bib77) 2020; 176
Muller, Mascagni, McDonald (bib32) 2009; 213
Grand, Abi Gerges, David, Diana, Paoletti (bib14) 2018; 9
Kleckner, Dingledine (bib21) 1988; 241
Otsu, Darcq, Pietrajtis, Mátyás, Schwartz, Bessaih, Abi Gerges, Rousseau, Grand, Dieudonné (bib38) 2019; 366
Gründemann, Lüthi (bib15) 2015; 35
Pérez-Otaño, Luján, Tavalin, Plomann, Modregger, Liu, Jones, Heinemann, Lo, Ehlers (bib47) 2006; 9
Javitt, Zukin (bib18) 1991; 148
Le Bail, Martineau, Sacchi, Yatsenko, Radzishevsky, Conrod, Ait Ouares, Wolosker, Pollegioni, Billard, Mothet (bib22) 2015; 112
Niewoehner, Single, Hvalby, Jensen, Meyer zum Alten Borgloh, Seeburg, Rawlins, Sprengel, Bannerman (bib36) 2007; 25
Murillo, Navarro, Puelles, Zhang, Petros, Pérez-Otaño (bib34) 2021; 31
Matsuzaki, Honkura, Ellis-Davies, Kasai (bib28) 2004; 429
Stringer, Pachitariu, Steinmetz, Reddy, Carandini, Harris (bib63) 2019; 364
Roberts, Díez-García, Rodriguiz, López, Luján, Martínez-Turrillas, Picó, Henson, Bernardo, Jarrett (bib54) 2009; 63
Shibasaki, Hosoi, Kaneko, Tominaga, Yamada (bib61) 2017; 140
Niell, Stryker (bib35) 2010; 65
Papouin, Ladépêche, Ruel, Sacchi, Labasque, Hanini, Groc, Pollegioni, Mothet, Oliet (bib44) 2012; 150
Tang, Kochubey, Kintscher, Schneggenburger (bib66) 2020; 40
Sasaki, Rothe, Premkumar, Das, Cui, Talantova, Wong, Gong, Chan, Zhang (bib59) 2002; 87
Paul, Crow, Raudales, He, Gillis, Huang (bib45) 2017; 171
References_xml – volume: 35
  start-page: 200
  year: 2015
  end-page: 206
  ident: bib15
  article-title: Ensemble coding in amygdala circuits for associative learning
  publication-title: Curr. Opin. Neurobiol.
– year: 2001
  ident: bib78
  article-title: The glycinergic inhibitory synapse
  publication-title: Cellular and Molecular Life Sciences CMLS
– volume: 364
  start-page: 255
  year: 2019
  ident: bib63
  article-title: Spontaneous behaviors drive multidimensional, brainwide activity
  publication-title: Science
– volume: 429
  start-page: 761
  year: 2004
  end-page: 766
  ident: bib28
  article-title: Structural basis of long-term potentiation in single dendritic spines
  publication-title: Nature
– volume: 87
  start-page: 1143
  year: 2015
  end-page: 1161
  ident: bib29
  article-title: Waking state: rapid variations modulate neural and behavioral responses
  publication-title: Neuron
– volume: 99
  start-page: 122
  year: 2008
  end-page: 132
  ident: bib67
  article-title: Modulation of NMDA receptor properties and synaptic transmission by the NR3A subunit in mouse hippocampal and cerebrocortical neurons
  publication-title: J. Neurophysiol.
– volume: 71
  start-page: 112
  year: 2007
  end-page: 122
  ident: bib2
  article-title: Subunit-specific roles of glycine-binding domains in activation of NR1/NR3
  publication-title: Mol. Pharmacol.
– volume: 19
  start-page: 1030
  year: 2013
  end-page: 1038
  ident: bib25
  article-title: Suppressing aberrant GluN3A expression rescues synaptic and behavioral impairments in Huntington’s disease models
  publication-title: Nat. Med.
– volume: 6
  start-page: e25492
  year: 2017
  ident: bib12
  article-title: Co-agonists differentially tune GluN2B-NMDA receptor trafficking at hippocampal synapses
  publication-title: eLife
– volume: 9
  start-page: 4769
  year: 2018
  ident: bib14
  article-title: Unmasking GluN1/GluN3A excitatory glycine NMDA receptors
  publication-title: Nat. Commun.
– volume: 325
  start-page: 529
  year: 1987
  end-page: 531
  ident: bib20
  article-title: Glycine potentiates the NMDA response in cultured mouse brain neurons
  publication-title: Nature
– volume: 15
  start-page: 6509
  year: 1995
  end-page: 6520
  ident: bib65
  article-title: Developmental and regional expression pattern of a novel NMDA receptor-like subunit (NMDAR-L) in the rodent brain
  publication-title: J. Neurosci.
– volume: 15
  start-page: 604
  year: 2016
  end-page: 608
  ident: bib6
  article-title: Photolysis quantum yield measurements in the near-UV; a critical analysis of 1-(2-nitrophenyl)ethyl photochemistry
  publication-title: Photochem. Photobiol. Sci.
– volume: 98
  start-page: 602
  year: 2018
  end-page: 615.e8
  ident: bib9
  article-title: Vision and locomotion shape the interactions between neuron types in mouse visual cortex
  publication-title: Neuron
– volume: 105
  start-page: 14163
  year: 2008
  end-page: 14168
  ident: bib69
  article-title: Rules of engagement for NMDA receptor subunits
  publication-title: Proc. Natl. Acad. Sci. USA
– volume: 17
  start-page: 623
  year: 2016
  end-page: 635
  ident: bib46
  article-title: Emerging roles of GluN3-containing NMDA receptors in the CNS
  publication-title: Nat. Rev. Neurosci.
– volume: 172
  start-page: 4254
  year: 2015
  end-page: 4276
  ident: bib23
  article-title: Ketamine and phencyclidine: the good, the bad and the unexpected
  publication-title: Br. J. Pharmacol.
– volume: 140
  start-page: 395
  year: 2017
  end-page: 403
  ident: bib61
  article-title: Glycine release from astrocytes via functional reversal of GlyT1
  publication-title: J. Neurochem.
– volume: 454
  start-page: 881
  year: 2008
  end-page: 885
  ident: bib51
  article-title: Internal brain state regulates membrane potential synchrony in barrel cortex of behaving mice
  publication-title: Nature
– volume: 482
  start-page: 123
  year: 2005
  end-page: 141
  ident: bib75
  article-title: Glycinergic neurons expressing enhanced green fluorescent protein in bacterial artificial chromosome transgenic mice
  publication-title: J. Comp. Neurol.
– volume: 363
  start-page: 413
  year: 2019
  end-page: 417
  ident: bib11
  article-title: Distinct molecular programs regulate synapse specificity in cortical inhibitory circuits
  publication-title: Science
– volume: 3
  start-page: a005678
  year: 2011
  ident: bib60
  article-title: The postsynaptic organization of synapses
  publication-title: Cold Spring Harbor Perspect. Biol.
– volume: 12
  start-page: 866
  year: 2013
  end-page: 885
  ident: bib16
  article-title: Glycine transporters as novel therapeutic targets in schizophrenia, alcohol dependence and pain
  publication-title: Nat. Rev. Drug Discov.
– volume: 366
  start-page: 250
  year: 2019
  end-page: 254
  ident: bib38
  article-title: Control of aversion by glycine-gated GluN1/GluN3A NMDA receptors in the adult medial habenula
  publication-title: Science
– volume: 9
  start-page: 611
  year: 2006
  end-page: 621
  ident: bib47
  article-title: Endocytosis and synaptic removal of NR3A-containing NMDA receptors by PACSIN1/syndapin1
  publication-title: Nat. Neurosci.
– volume: 14
  start-page: 383
  year: 2013
  end-page: 400
  ident: bib42
  article-title: NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease
  publication-title: Nat. Rev. Neurosci.
– volume: 56
  start-page: 8197
  year: 2000
  end-page: 8205
  ident: bib43
  article-title: Effects of aromatic substituents on the photocleavage of 1-acyl-7-nitroindolines
  publication-title: Tetrahedron
– volume: 85
  start-page: 68
  year: 2015
  end-page: 75
  ident: bib41
  article-title: In vivo measurement of cell-type-specific synaptic connectivity and synaptic transmission in layer 2/3 mouse barrel cortex
  publication-title: Neuron
– volume: 84
  start-page: 355
  year: 2014
  end-page: 362
  ident: bib52
  article-title: Pupil fluctuations track fast switching of cortical states during quiet wakefulness
  publication-title: Neuron
– volume: 40
  start-page: 3969
  year: 2020
  end-page: 3980
  ident: bib66
  article-title: A VTA to basal amygdala dopamine projection contributes to signal salient somatosensory events during fear learning
  publication-title: J. Neurosci.
– volume: 6
  start-page: 314
  year: 2011
  end-page: 326
  ident: bib10
  article-title: A practical guide to the synthesis of dinitroindolinyl-caged neurotransmitters
  publication-title: Nat. Protoc.
– volume: 62
  start-page: 159
  year: 1994
  end-page: 165
  ident: bib71
  article-title: Concentrations of amino acids in extracellular fluid after opening of the blood-brain barrier by intracarotid infusion of protamine sulfate
  publication-title: J. Neurochem.
– volume: 5
  start-page: e14985
  year: 2016
  ident: bib40
  article-title: Behavioral-state modulation of inhibition is context-dependent and cell type specific in mouse visual cortex
  publication-title: eLife
– volume: 14
  start-page: 719
  year: 2009
  end-page: 727
  ident: bib3
  article-title: Targeted disruption of serine racemase affects glutamatergic neurotransmission and behavior
  publication-title: Mol. Psychiatry
– volume: 241
  start-page: 835
  year: 1988
  end-page: 837
  ident: bib21
  article-title: Requirement for glycine in activation of NMDA-receptors expressed in
  publication-title: Science
– volume: 93
  start-page: 281
  year: 2017
  end-page: 290
  ident: bib79
  article-title: A Brief History of Long-Term Potentiation
  publication-title: Neuron
– volume: 63
  start-page: 342
  year: 2009
  end-page: 356
  ident: bib54
  article-title: Downregulation of NR3A-containing NMDARs is required for synapse maturation and memory consolidation
  publication-title: Neuron
– volume: 150
  start-page: 633
  year: 2012
  end-page: 646
  ident: bib44
  article-title: Synaptic and extrasynaptic NMDA receptors are gated by different endogenous coagonists
  publication-title: Cell
– volume: 65
  start-page: 472
  year: 2010
  end-page: 479
  ident: bib35
  article-title: Modulation of visual responses by behavioral state in mouse visual cortex
  publication-title: Neuron
– volume: 213
  start-page: 275
  year: 2009
  end-page: 288
  ident: bib32
  article-title: Dopaminergic innervation of pyramidal cells in the rat basolateral amygdala
  publication-title: Brain Struct. Funct.
– volume: 571
  start-page: 361
  year: 2019
  end-page: 365
  ident: bib62
  article-title: High-dimensional geometry of population responses in visual cortex
  publication-title: Nature
– volume: 373
  start-page: 151
  year: 1995
  end-page: 155
  ident: bib57
  article-title: Reduced hippocampal LTP and spatial learning in mice lacking NMDA receptor epsilon 1 subunit
  publication-title: Nature
– volume: 80
  start-page: 1025
  year: 2013
  end-page: 1038
  ident: bib74
  article-title: Expression of cocaine-evoked synaptic plasticity by GluN3A-containing NMDA receptors
  publication-title: Neuron
– volume: 14
  start-page: 861
  year: 2018
  end-page: 869
  ident: bib76
  article-title: Monitoring hippocampal glycine with the computationally designed optical sensor GlyFS
  publication-title: Nat. Chem. Biol.
– volume: 62
  start-page: 1119
  year: 2002
  end-page: 1127
  ident: bib1
  article-title: Association of NR3A with the
  publication-title: Mol. Pharmacol.
– volume: 354
  start-page: 102
  year: 2007
  end-page: 108
  ident: bib24
  article-title: Principal role of NR3 subunits in NR1/NR3 excitatory glycine receptor function
  publication-title: Biochem. Biophys. Res. Commun.
– volume: 16
  start-page: 1864
  year: 2013
  end-page: 1869
  ident: bib58
  article-title: Integration of visual motion and locomotion in mouse visual cortex
  publication-title: Nat. Neurosci.
– volume: 31
  start-page: 1914
  year: 2021
  end-page: 1926
  ident: bib34
  article-title: Temporal dynamics and neuronal specificity of Grin3a expression in the mouse forebrain
  publication-title: Cereb. Cortex
– volume: 176
  start-page: 108117
  year: 2020
  ident: bib77
  article-title: Negative allosteric modulation of GluN1/GluN3 NMDA receptors
  publication-title: Neuropharmacology
– volume: 87
  start-page: 2052
  year: 2002
  end-page: 2063
  ident: bib59
  article-title: Characterization and comparison of the NR3A subunit of the NMDA receptor in recombinant systems and primary cortical neurons
  publication-title: J. Neurophysiol.
– volume: 193
  start-page: 108631
  year: 2021
  ident: bib64
  article-title: Glycine agonism in ionotropic glutamate receptors
  publication-title: Neuropharmacology
– volume: 171
  start-page: 522
  year: 2017
  end-page: 539.e20
  ident: bib45
  article-title: Transcriptional architecture of synaptic communication delineates GABAergic neuron identity
  publication-title: Cell
– volume: 600
  start-page: 261
  year: 2022
  end-page: 276
  ident: bib7
  article-title: GluN3A NMDA receptor subunits: more enigmatic than ever?
  publication-title: J. Physiol.
– volume: 393
  start-page: 377
  year: 1998
  end-page: 381
  ident: bib8
  article-title: Increased NMDA current and spine density in mice lacking the NMDA receptor subunit NR3A
  publication-title: Nature
– volume: 508
  start-page: 207
  year: 2014
  end-page: 214
  ident: bib37
  article-title: A mesoscale connectome of the mouse brain
  publication-title: Nature
– year: 2017
  ident: bib39
  article-title: Suite2p: beyond 10,000 neurons with standard two-photon microscopy
  publication-title: bioRxiv
– volume: 457
  start-page: 1015
  year: 2009
  end-page: 1018
  ident: bib55
  article-title: Synaptic depression enables neuronal gain control
  publication-title: Nature
– volume: 80
  start-page: 143
  year: 2013
  end-page: 158
  ident: bib70
  article-title: Cytosolic transmitter concentration regulates vesicle cycling at hippocampal GABAergic terminals
  publication-title: Neuron
– volume: 71
  start-page: 361
  year: 2004
  end-page: 370
  ident: bib31
  article-title: NR3A NMDA receptor subunit mRNA expression in schizophrenia, depression and bipolar disorder
  publication-title: Schizophr. Res.
– volume: 38
  start-page: 6983
  year: 2018
  end-page: 7003
  ident: bib53
  article-title: Vasoactive intestinal polypeptide-immunoreactive interneurons within circuits of the mouse basolateral amygdala
  publication-title: J. Neurosci.
– volume: 15
  start-page: 607
  year: 2012
  end-page: 612
  ident: bib13
  article-title: Unique functional properties of somatostatin-expressing GABAergic neurons in mouse barrel cortex
  publication-title: Nat. Neurosci.
– volume: 62
  start-page: 405
  year: 2010
  end-page: 496
  ident: bib68
  article-title: Glutamate receptor ion channels: structure, regulation, and function
  publication-title: Pharmacol. Rev.
– volume: 15
  start-page: 6498
  year: 1995
  end-page: 6508
  ident: bib5
  article-title: Cloning and characterization of chi-1: a developmentally regulated member of a novel class of the ionotropic glutamate receptor family
  publication-title: J Neurosci
– volume: 11
  start-page: 5038
  year: 2020
  ident: bib50
  article-title: Identification of epilepsy-associated neuronal subtypes and gene expression underlying epileptogenesis
  publication-title: Nat. Commun.
– volume: 355
  start-page: 954
  year: 2017
  end-page: 959
  ident: bib33
  article-title: Layer-specific modulation of neocortical dendritic inhibition during active wakefulness
  publication-title: Science
– volume: 25
  start-page: 837
  year: 2007
  end-page: 846
  ident: bib36
  article-title: Impaired spatial working memory but spared spatial reference memory following functional loss of NMDA receptors in the dentate gyrus
  publication-title: Eur. J. Neurosci.
– volume: 26
  start-page: 4559
  year: 2006
  end-page: 4566
  ident: bib73
  article-title: Characterization of a soluble ligand binding domain of the NMDA receptor regulatory subunit NR3A
  publication-title: J. Neurosci.
– volume: 567
  start-page: 100
  year: 2019
  end-page: 104
  ident: bib72
  article-title: Neuromodulatory control of localized dendritic spiking in critical period cortex
  publication-title: Nature
– volume: 148
  start-page: 1301
  year: 1991
  end-page: 1308
  ident: bib18
  article-title: Recent advances in the phencyclidine model of schizophrenia
  publication-title: Am. J. Psychiatry
– volume: 6
  start-page: 255
  year: 2010
  end-page: 257
  ident: bib27
  article-title: Two-photon uncaging of γ-aminobutyric acid in intact brain tissue
  publication-title: Nat. Chem. Biol.
– volume: 26
  start-page: 1965
  year: 2018
  end-page: 1972
  ident: bib26
  article-title: RNAi-based GluN3A silencing prevents and reverses disease phenotypes induced by mutant huntingtin
  publication-title: Mol. Ther.
– volume: 147
  start-page: 509
  year: 2011
  end-page: 524
  ident: bib19
  article-title: Molecular mechanisms of fear learning and memory
  publication-title: Cell
– volume: 16
  start-page: 1068
  year: 2013
  end-page: 1076
  ident: bib49
  article-title: Inhibition of inhibition in visual cortex: the logic of connections between molecularly distinct interneurons
  publication-title: Nat. Neurosci.
– volume: 415
  start-page: 793
  year: 2002
  end-page: 798
  ident: bib4
  article-title: Excitatory glycine receptors containing the NR3 family of NMDA receptor subunits
  publication-title: Nature
– volume: 112
  start-page: E204
  year: 2015
  end-page: E213
  ident: bib22
  article-title: Identity of the NMDA receptor coagonist is synapse specific and developmentally regulated in the hippocampus
  publication-title: Proc. Natl. Acad. Sci. USA
– volume: 97
  start-page: 4926
  year: 2000
  end-page: 4931
  ident: bib30
  article-title: D-serine is an endogenous ligand for the glycine site of the
  publication-title: Proc. Natl. Acad. Sci. USA
– volume: 21
  start-page: 1228
  year: 2001
  end-page: 1237
  ident: bib48
  article-title: Assembly with the NR1 subunit is required for surface expression of NR3A-containing NMDA receptors
  publication-title: J. Neurosci.
– volume: 12
  start-page: 14
  year: 2018
  ident: bib56
  article-title: NeuroMatic: an integrated open-source software toolkit for acquisition, analysis and simulation of electrophysiological data
  publication-title: Front. Neuroinform.
– volume: 573
  start-page: 61
  year: 2019
  end-page: 68
  ident: bib17
  article-title: Conserved cell types with divergent features in human versus mouse cortex
  publication-title: Nature
SSID ssj0014591
Score 2.5394309
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...
SourceID pubmedcentral
hal
proquest
pubmed
elsevier
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 2438
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
Volume 110
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Nb9QwEB2VIiQuFW352JZWBiFu0Tq2EyfHUFFWFCrxUbE3y46dNqjNrra7Ffn3jJ2kInDjaMeJE48zfraf3wC8yTKBw0qmoypPXCRyoSPDJYuM1AnekjAbwr19Pk9nF-LjPJlvwclwFsbTKnvf3_n04K37nGnfmtNlXU-_0Sz36uXYIz0ukV7xk4ssHOKbv7vfSRBJFzUPC0e-9HB8LnC8gmakV0FlrNPvTEdj0oMrT478F3n-TaD8Y0Q6fQI7PZQkRfe2u7Dlmj3YLxqcRt-05C0J5M6war4Hj7qYk-0-fPlwvTnnBXG_Sn-8bLFqyeV167fXCTaEW_roO6QnsJOgzoGpVVjxJrqxRN-0l1bjfJiU9arc1Ovbp3Bx-v77ySzq4ypEDt3iOtKVrlItKLclTv6s0BJRkUtLahCuGYtzIJmYyjHH45LLKs0sq4QzlTUIT_KS8mew3Swa9wKINSbNNM-tlLEoU5NLauLEMqc1zaqYTkAOzalGZlXosdXAMPupOkMobwhFE4WZE3iNra-WneaG8irYs-KT8nmUI6zBMfUunsCrwTgKfwu_16Ebt9jcKuapuwyxST6B552x7p_Fvaa_5FiFHJlxVNn4SlNfBentnKfotMTBf3_WITz2qUAh5C9he73auCOENWtzDA-Ls68_zo5D__0NRlz56w
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1db9MwFL3ahhC8TLDx0fFlEOItqmM7cfJYJkYHXSXEJvXNsmNnC9rSqmsR-fdcO8lE4I3H2E6c-DrXx_bxuQDvs0zgsJLpqMwTF4lc6MhwySIjdYK3JMyGcG9n83R6Ib4sksUOHPdnYTytsvP9rU8P3rpLGXetOV5V1fg7zXKvXo490uMSyXfhHqIB6eM3nC4-3m0liKQNm4elI1-8Pz8XSF5BNNLLoDLWCnimg0Fp98qzI_-Fnn8zKP8Ykk4ewX6HJcmkfd3HsOPqAzic1DiPvmnIBxLYnWHZ_ADut0Enm0P49vl6O-cT4n4V_nzZct2Qy-vG768TbAm38uF3SMdgJ0GeA6_WYcmb6NoSfdNcWo0TYlJU62JbbW6fwMXJp_PjadQFVogc-sVNpEtdplpQbguc_VmhJcIilxbUIF4zFidBMjGlY47HBZdlmllWCmdKaxCf5AXlT2GvXtbuORBrTJppnlspY1GkJpfUxIllTmualTEdgeybUw3sqtBlq55i9kO1hlDeEIomChNH8A5bX61a0Q3lZbCnk5nyaZQjrsFB9Wc8gre9cRT-F36zQ9duub1VzHN3GYKTfATPWmPdPYt7UX_JsQo5MOOgsmFOXV0F7e2cp-i1xNF_f9YbeDA9P5up2en86wt46HMCn5C_hL3NeuteIcbZmNehD_8G-PH7Zw
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=GluN3A+excitatory+glycine+receptors+control+adult+cortical+and+amygdalar+circuits&rft.jtitle=Neuron+%28Cambridge%2C+Mass.%29&rft.au=Bossi%2C+Simon&rft.au=Dhanasobhon%2C+Dhanasak&rft.au=Ellis-Davies%2C+Graham+C+R&rft.au=Frontera%2C+Jimena&rft.date=2022-08-03&rft.pub=Elsevier&rft.issn=0896-6273&rft.volume=110&rft.issue=15&rft.spage=2438&rft.epage=2454.e8&rft_id=info:doi/10.1016%2Fj.neuron.2022.05.016&rft_id=info%3Apmid%2F35700736&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=oai_HAL_hal_03782718v1
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0896-6273&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0896-6273&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0896-6273&client=summon