The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
GluN2D-Containing N-methyl-d-Aspartate Receptors Mediate Synaptic Transmission in Hippocampal Interneurons and Regulate Interneuron Activity
Open accessAbstract
N-methyl-d-aspartate receptors (NMDARs) are ionotropic glutamatergic receptors that have been implicated in learning, development, and neuropathological conditions. They are typically composed of GluN1 and GluN2A-D subunits. Whereas a great deal is known about the role of GluN2A- and GluN2B-containing NMDARs, much less is known about GluN2D-containing NMDARs. Here we explore the subunit composition of synaptic NMDARs on hippocampal interneurons. GluN2D mRNA was detected by single-cell PCR and in situ hybridization in diverse interneuron subtypes in the CA1 region of the hippocampus. The GluN2D subunit was detectable by immunoblotting and immunohistochemistry in all subfields of the hippocampus in young and adult mice. In whole-cell patch-clamp recordings from acute hippocampal slices, (+)-CIQ, the active enantiomer of the positive allosteric modulator CIQ, significantly enhanced the amplitude of the NMDAR component of miniature excitatory postsynaptic currents (mEPSCs) in CA1 interneurons but not in pyramidal cells. (+)-CIQ had no effect in slices from Grin2d-/- mice, suggesting that GluN2D-containing NMDARs participate in excitatory synaptic transmission onto hippocampal interneurons. The time course of the NMDAR component of the mEPSC was unaffected by (+)-CIQ potentiation and was not accelerated in slices from Grin2d-/- mice compared with wild-type, suggesting that GluN2D does not detectably slow the NMDAR EPSC time course at this age. (+)-CIQ increased the activity of CA1 interneurons as detected by the rate and net charge transfer of spontaneous inhibitory postsynaptic currents (sIPSCs) recorded from CA1 pyramidal cells. These data provide evidence that interneurons contain synaptic NMDARs possessing a GluN2D subunit, which can influence interneuron function and signal processing.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Furthermore, Grin2d has been found in hippocampal interneurons and enhances their activity due to its involvement in synaptic transmission66.”
From Elimination of the four extracellular matrix molecules tenascin-C, tenascin-R, brevican and neurocan alters the ratio of excitatory and inhibitory synapses (2019) · cites this paper as [66]
In the citing paper
“In addition, ketamine is reported to have higher affinity for GluN2D NMDAR subunits 40, 41, which are highly expressed in forebrain inhibitory interneurons 42, 43.”
From Mechanisms of ketamine action as an antidepressant (2018) · cites this paper as [43]
Citations
Cites
Glutamate Receptor Ion Channels: Structure, Regulation, and Function
Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568
Self-citationMonyer, H., Burnashev, N., Laurie, D. J., Sakmann, B., & Seeburg, P. H. (1994) · Neuron · doi:10.1016/0896-6273(94)90210-0 · Cited by 3,535
Choi, D. W. (1992) · Journal of Neurobiology · doi:10.1002/neu.480230915 · Cited by 2,329
Functional Repression of cAMP Response Element in 6-Hydroxydopamine-treated Neuronal Cells
Chalovich, E. M., Zhu, J.-H., Caltagarone, J., Bowser, R., & Chu, C. T. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602632200 · Cited by 1,385
Automated design of ligands to polypharmacological profiles
Besnard, J., Ruda, G. F., Setola, V., Abecassis, K., Rodriguiz, R. M., Huang, X.-P., Norval, S., Sassano, M. F., Shin, A. I., Webster, L. A., et al. (2012) · Nature · doi:10.1038/nature11691 · Cited by 832
Molecular and Physiological Diversity of Cortical Nonpyramidal Cells
Cauli, B., Audinat, E., Lambolez, B., Angulo, M. C., Ropert, N., Tsuzuki, K., Hestrin, S., & Rossier, J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03894.1997 · Cited by 738
Functional and Pharmacological Differences Between Recombinant N -Methyl- d -Aspartate Receptors
Vicini, S., Wang, J. F., Li, J. H., Zhu, W. J., Wang, Y. H., Luo, J. H., Wolfe, B. B., & Grayson, D. R. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.2.555 · Cited by 674
Channel kinetics determine the time course of NMDA receptor-mediated synaptic currents
Lester, R. A. J., Clements, J. D., Westbrook, G. L., & Jahr, C. E. (1990) · Nature · doi:10.1038/346565a0 · Cited by 564
AMPA receptor subunits expressed by single purkinje cells
Lambolez, B., Audinat, É., Bochet, P., Crépel, F., & Rossier, J. (1992) · Neuron · doi:10.1016/0896-6273(92)90164-9 · Cited by 553
Preskorn, S., Baker, B., Kolluri, S., Menniti, F. S., Krams, M., & Landen, J. W. (2008) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0b013e31818a6cea · Cited by 524
Akazawa, C., Shigemoto, R., Bessho, Y., Nakanishi, S., & Mizuno, N. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903470112 · Cited by 506
Converging Evidence of NMDA Receptor Hypofunction in the Pathophysiology of Schizophrenia
Coyle, J. T., Tsai, G. E., & GOFF, D. C. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.020 · Cited by 443
NMDA Receptor and Schizophrenia: A Brief History
COYLE, J. T. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs076 · Cited by 432
Lacaille, J., Mueller, A., Kunkel, D., & Schwartzkroin, P. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-07-01979.1987 · Cited by 388
Standaert, D. G., Testa, C. M., Young, A. B., & Penney, J. B. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903430102 · Cited by 373
Neural plasticity and behavior – sixty years of conceptual advances
Sweatt, J. D. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13580 · Cited by 364
Long-term synaptic plasticity in hippocampal interneurons
Kullmann, D. M., & Lamsa, K. P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2207 · Cited by 340
NMDA receptor subunit mRNA expression by projection neurons and interneurons in rat striatum
Landwehrmeyer, G. B., Standaert, D. G., Testa, C. M., Penney, J., & Young, A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05297.1995 · Cited by 316
Classification of fusiform neocortical interneurons based on unsupervised clustering
Cauli, B., Porter, J. T., Tsuzuki, K., Lambolez, B., Rossier, J., Quenet, B., & Audinat, E. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.11.6144 · Cited by 316
Liu, X.-B., Murray, K. D., & Jones, E. G. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2476-04.2004 · Cited by 313
Hansen, K. B., Ogden, K. K., Yuan, H., & Traynelis, S. F. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.035 · Cited by 300
Self-citationInfluence of GluN2 subunit identity on NMDA receptor function
Wyllie, D. J. A., Livesey, M. R., & Hardingham, G. E. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.01.016 · Cited by 260
The NMDA receptor as a target for cognitive enhancement
Collingridge, G. L., Volianskis, A., Bannister, N. J., France, G., Hanna, L., Mercier, M., Tidball, P., Fang, G., Irvine, M. W., Costa, B. M., et al. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.051 · Cited by 255
Pelkey, K. A., Barksdale, E., Craig, M. T., Yuan, X., Sukumaran, M., Vargish, G. A., Mitchell, R. M., Wyeth, M. S., Petralia, R. S., Chittajallu, R., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.020 · Cited by 245
Self-citationRationale for and use of NMDA receptor antagonists in Parkinson's disease
Hallett, P. J., & Standaert, D. G. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.04.001 · Cited by 238
McBain, C. J., & Dingledine, R. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019560 · Cited by 221
Self-citationIonotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases
Yuan, H., Low, C., Moody, O. A., Jenkins, A., & Traynelis, S. F. (2015) · Molecular Pharmacology · doi:10.1124/mol.115.097998 · Cited by 208
Self-citationPRESKORN, S., MACALUSO, M., MEHRA, D. V., ZAMMIT, G., MOSKAL, J. R., & BURCH, R. M. (2015) · Journal of Psychiatric Practice · doi:10.1097/01.pra.0000462606.17725.93 · Cited by 193
mGluR7 Is a Metaplastic Switch Controlling Bidirectional Plasticity of Feedforward Inhibition
Pelkey, K. A., Lavezzari, G., Racca, C., Roche, K. W., & McBain, C. J. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.011 · Cited by 178
Self-citationPorter, J. T., Cauli, B., Staiger, J. F., Lambolez, B., Rossier, J., & Audinat, E. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00367.x · Cited by 173
Standaert, D. G., Landwehrmeyer, G. B., Kerner, J. A., Penney, J. B., & Young, A. B. (1996) · Molecular Brain Research · doi:10.1016/s0169-328x(96)00117-9 · Cited by 171
A subunit-selective potentiator of NR2C- and NR2D-containing NMDA receptors
Mullasseril, P., Hansen, K. B., Vance, K. M., Ogden, K. K., Yuan, H., Kurtkaya, N. L., Santangelo, R., Orr, A. G., Le, P., Vellano, K. M., et al. (2010) · Nature Communications · doi:10.1038/ncomms1085 · Cited by 158
Self-citationNeuroprotection by NMDA Receptor Antagonists in a Variety of Neuropathologies
Palmer, G. C. (2001) · Current Drug Targets · doi:10.2174/1389450013348335 · Cited by 146
Glycine-independent and subunit-specific potentiation of NMDA responses by extracellular Mg2+
Paoletti, P., Neyton, J., & Ascher, P. (1995) · Neuron · doi:10.1016/0896-6273(95)90099-3 · Cited by 131
Mechanisms Underlying the Rules for Associative Plasticity at Adult Human Neocortical Synapses
Verhoog, M. B., Goriounova, N. A., Obermayer, J., Stroeder, J., Hjorth, J. J. J., Testa-Silva, G., Baayen, J. C., de Kock, C. P. J., Meredith, R. M., & Mansvelder, H. D. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3158-13.2013 · Cited by 127
Pelkey, K. A., Topolnik, L., Lacaille, J.-C., & McBain, C. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.032 · Cited by 115
Self-citationDevelopmental origin dictates interneuron AMPA and NMDA receptor subunit composition and plasticity
Matta, J. A., Pelkey, K. A., Craig, M. T., Chittajallu, R., Jeffries, B. W., & McBain, C. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3459 · Cited by 108
Self-citationEngelhardt, J. V., Bocklisch, C., Tönges, L., Herb, A., Mishina, M., & Monyer, H. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00095 · Cited by 103
Eye Opening Rapidly Induces Synaptic Potentiation and Refinement
Lü, W., & Constantine‐Paton, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.031 · Cited by 101
Retchless, B. S., Gao, W., & Johnson, J. W. (2012) · Nature Neuroscience · doi:10.1038/nn.3025 · Cited by 99
Hansen, K. B., Tajima, N., Risgaard, R., Perszyk, R. E., Jørgensen, L. M., Vance, K. M., Ogden, K. K., Clausen, R. P., Furukawa, H., & Traynelis, S. F. (2013) · Molecular Pharmacology · doi:10.1124/mol.113.085803 · Cited by 95
Self-citationNMDA Receptor NR2 Subunit Dependence of the Slow Component of Magnesium Unblock
Clarke, R. J., & Johnson, J. W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0577-06.2006 · Cited by 89
Edman, S. J., McKay, S., Macdonald, L. J., Samadi, M., Livesey, M. R., Hardingham, G. E., & Wyllie, D. J. A. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.04.027 · Cited by 85
Kew, J. N. C., & Kemp, J. A. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.017bf.x · Cited by 80
The role of inhibition in human motor cortical plasticity
Bachtiar, V., & Stagg, C. J. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.059 · Cited by 79
GluN2B and GluN2D NMDARs dominate synaptic responses in the adult spinal cord
Hildebrand, M. E., Pitcher, G. M., Harding, E. K., Li, H., Beggs, S., & Salter, M. W. (2014) · Scientific Reports · doi:10.1038/srep04094 · Cited by 78
NMDA Receptors Containing the GluN2D Subunit Control Neuronal Function in the Subthalamic Nucleus
Swanger, S. A., Vance, K. M., Paré, J., Sotty, F., Fog, K., Smith, Y., & Traynelis, S. F. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1702-15.2015 · Cited by 77
Self-citationThompson, C. L., Drewery, D. L., Atkins, H. D., Stephenson, F. A., & Chazot, P. L. (2002) · Molecular Brain Research · doi:10.1016/s0169-328x(02)00183-3 · Cited by 75
Xue, J.-G., Masuoka, T., Gong, X.-D., Chen, K., Yanagawa, Y., Law, S. K. A., & Konishi, S. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00287.2010 · Cited by 75
GluN1 splice variant control of GluN1/GluN2D NMDA receptors
Vance, K. M., Hansen, K. B., & Traynelis, S. F. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.234062 · Cited by 69
Self-citationExpression of N-methyl- d-aspartate glutamate receptor subunits in the prefrontal cortex of the rat
Rudolf, G., Cronin, C. A., Landwehrmeyer, G. B., Standaert, D. G., Penney, J., & Young, A. B. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00048-6 · Cited by 49
Santangelo, R., Ogden, K. K., Strong, K. L., Khatri, A., Chepiga, K. M., Jensen, H. S., Traynelis, S. F., & Liotta, D. C. (2013) · Journal of Medicinal Chemistry · doi:10.1021/jm400177t · Cited by 48
Self-citationMcKay, S., Griffiths, N., Butters, P., Thubron, E., Hardingham, G. E., & Wyllie, D. J. A. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01748.x · Cited by 38
Depolarization gates spine calcium transients and spike-timing-dependent potentiation
Jiang, H., & Oertner, T. G. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.10.004 · Cited by 29
Marani, T. H. E., Marani, E., Heida, T., Lakke, E. A. J. F., & Usunoff, K. G. (2008) · Cited by 25
Modal gating of GluN1/GluN2D NMDA receptors
Vance, K. M., Hansen, K. B., & Traynelis, S. F. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.03.018 · Cited by 19
Self-citationStefanescu, R. A., & Shore, S. E. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00075 · Cited by 17
Talaei, S. A., Azami, A., & Salami, M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.01.024 · Cited by 10
Santangelo, R., Ogden, K. K., Strong, K. L., Khatri, A., Chepiga, K. M., Jensen, H. S., Traynelis, S. F., & Liotta, D. C. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm500710w · Cited by 9
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Mechanisms of ketamine action as an antidepressant
Zanos, P., & Gould, T. D. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.255 · Cited by 1,127
Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889
Self-citationStructure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686
Self-citationThe Role of NMDA Receptors in Alzheimer’s Disease
Liu, J., Chang, L., Song, Y., Li, H., & Wu, Y. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00043 · Cited by 535
Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies
Oyrer, J., Maljevic, S., Scheffer, I. E., Berkovic, S. F., Petrou, S., & Reid, C. A. (2018) · Pharmacological Reviews · doi:10.1124/pr.117.014456 · Cited by 315
Metadata
- Authors
- Perszyk, R. E., DiRaddo, J. O., Strong, K. L., Low, C.-M., Ogden, K. K., Khatri, A., Vargish, G. A., Pelkey, K. A., Tricoire, L., Liotta, D. C., Smith, Y., McBain, C. J., & Traynelis, S. F.
- Affiliations
- National Institutes of Health (US)
- ORCID
- Venue
- Molecular Pharmacology
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 90
- Issue
- 6
- Pages
- 689-702
- ISSN
- 0026-895X (ISSN-L)
- PMC
- PMC5118640
- OpenAlex
- W2548997185
- Cited by
- 116
- References
- 59
- Citations by year
- 2026: 12 · 2025: 14 · 2024: 9 · 2023: 11 · 2022: 11 · 2021: 13 · 2020: 15 · 2019: 13 · 2018: 9 · 2017: 8 · 2016: 1
- FWCI
- 5.98
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Pharmacology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- University of Florida
- National Institutes of Health (P51OD011132)
- National Institute of General Medical Sciences (T32GM008602)
- National Institute of Neurological Disorders and Stroke (R01NS065371, R01NS036654)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- GluN2D, NMDA receptor, hippocampal interneurons, synaptic transmission, positive allosteric modulation, miniature excitatory postsynaptic currents, spontaneous inhibitory postsynaptic currents, CA1, glutamatergic synapses
- MeSH terms
- Allosteric Regulation, Animals, Hippocampus, Interneurons, Isoquinolines, Mice, Inbred C57BL, Synaptic Transmission, RNA, Messenger, Stereoisomerism, Time Factors, Xenopus laevis, Ion Channel Gating, Receptors, N-Methyl-D-Aspartate, Excitatory Postsynaptic Potentials, Rats, CA1 Region, Hippocampal, Real-Time Polymerase Chain Reaction
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review