Evidence map›Paper›PMID 24431445›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Phosphorylation of Ser1166 on GluN2B by PKA is critical to synaptic NMDA receptor function and Ca2+ signaling in spines.

Jessica A Murphy, Ivar S Stein, C Geoffrey Lau, Rui T Peixoto, Teresa K Aman, Naoki Kaneko, Kelly Aromolaran, Jessica L Saulnier, Gabriela K Popescu, Bernardo L Sabatini and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
5.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 113 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Dynamic control of NMDA receptor CaProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Neural Processing without OPhysiology (Bethesda, Md.) · 2024
    Review
  9. Amyloid-β Causes NMDA Receptor Dysfunction and Dendritic Spine Loss through mGluR1 and AKAP150-Anchored Calcineurin Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  10. d-Serine Inhibits Non-ionotropic NMDA Receptor Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  11. Review
  12. Plasticity in the Functional Properties of NMDA Receptors Improves Network Stability during Severe Energy Stress.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  13. Review
  14. Estimating the CaMethods in molecular biology (Clifton, N.J.) · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 1 country.

Jessica A MurphyDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461, Department of Pharmacology, University of California, Davis, California 95616, Department of Neurobiology, HHMI, Harvard Medical School, Boston, Massachusetts 02115, and Department of Biochemistry, University of Buffalo, State University of New York, Buffalo, New York 14214.
Ivar S Stein
C Geoffrey Lau
Rui T Peixoto
Teresa K Aman
Naoki Kaneko
Kelly Aromolaran
Jessica L Saulnier
Gabriela K Popescu
Bernardo L Sabatini
Johannes W Hell
R Suzanne Zukin
Yeshiva University · USAlbert Einstein College of Medicine · USHarvard University · USUniversity of California, Davis · USBuffalo State University · USHarvard University Press · USUniversity at Buffalo, State University of New York · US

Funding

REST-Activated Program of Gene Expression in IschemiaR01NS046742 · NINDS · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI ZUKIN, R. SUZANNE · 2004 to 2019
$6.1M
Dendritic Ca signals in striatal medium spiny neuronsR01NS046579 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SABATINI, BERNARDO L · 2004 to 2016
$5.0M
Probing allosteric surfaces of NMDA receptorsR01NS052669 · NINDS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI POPESCU, GABRIELA K · 2006 to 2015
$3.4M
Predoctoral Training in Pharmacological SciencesT32GM099608 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2021
$2.2M
Signaling by cAMP within postsynaptic nano domains R01NS078792R01NS078792 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2016
$2.0M
Permeation Mechanisms in NMDA receptorsR01NS097016 · NINDS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI POPESCU, GABRIELA K · 2016 to 2019
$1.4M
Protein kinase A modulation of NMDA receptor gating and permeabilityF32NS077622 · NINDS · UNIVERSITY OF WASHINGTON · PI AMAN, TERESA K · 2012 to 2014
$156k
NIGMS NIH HHS T32 GM099608NINDS NIH HHS F32 NS077622NINDS NIH HHS R01 NS046579NINDS NIH HHS R01 NS046742NINDS NIH HHS R01 NS052669NINDS NIH HHS R01 NS078792NINDS NIH HHS R01 NS097016
6 · The paper itself

Abstract

The NMDA-type glutamate receptor (NMDAR) is essential for synaptogenesis, synaptic plasticity, and higher cognitive function. Emerging evidence indicates that NMDAR Ca(2+) permeability is under the control of cAMP/protein kinase A (PKA) signaling. Whereas the functional impact of PKA on NMDAR-dependent Ca(2+) signaling is well established, the molecular target remains unknown. Here we identify serine residue 1166 (Ser1166) in the carboxy-terminal tail of the NMDAR subunit GluN2B to be a direct molecular and functional target of PKA phosphorylation critical to NMDAR-dependent Ca(2+) permeation and Ca(2+) signaling in spines. Activation of β-adrenergic and D1/D5-dopamine receptors induces Ser1166 phosphorylation. Loss of this single phosphorylation site abolishes PKA-dependent potentiation of NMDAR Ca(2+) permeation, synaptic currents, and Ca(2+) rises in dendritic spines. We further show that adverse experience in the form of forced swim, but not exposure to fox urine, elicits striking phosphorylation of Ser1166 in vivo, indicating differential impact of different forms of stress. Our data identify a novel molecular and functional target of PKA essential to NMDAR-mediated Ca(2+) signaling at synapses and regulated by the emotional response to stress.

Indexed as

AnimalsAnimals, NewbornCalcium SignalingCells, CulturedCyclic AMP-Dependent Protein KinasesDendritic SpinesFoxesHEK293 CellsHippocampusHumansNeural InhibitionPhosphorylationRats, Sprague-DawleyReceptors, N-Methyl-D-AspartateSerineStress, PsychologicalCyclic AMP-Dependent Protein KinasesNR2B NMDA receptorReceptors, N-Methyl-D-AspartateSerine

Identifiers

PMID24431445
PMCPMC3891964
OpenAlexW2040704538

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.