Evidence map›Paper›PMID 26475861›Full record

ArticleThe Journal of biological chemistry2015

Early Growth Response 1 (Egr-1) Regulates N-Methyl-d-aspartate Receptor (NMDAR)-dependent Transcription of PSD-95 and α-Amino-3-hydroxy-5-methyl-4-isoxazole Propionic Acid Receptor (AMPAR) Trafficking in Hippocampal Primary Neurons.

Xike Qin, Yongjun Jiang, Yiu Chung Tse, Yunling Wang, Tak Pan Wong, Hemant K Paudel

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

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  10. Altered Expression andCurrent neuropharmacology · 2022
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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

6 authors at 2 institutions in 1 country.

Xike QinFrom The Bloomfield Center for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, and.
Yongjun JiangFrom The Bloomfield Center for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, and Department of Neurology and Neurosurgery.
Yiu Chung TseDouglas Mental Health University Institute, and Department of Psychiatry, McGill University, Montréal, Quebec H4H 1R3, Canada.
Yunling WangFrom The Bloomfield Center for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, and.
Tak Pan WongDouglas Mental Health University Institute, and Department of Psychiatry, McGill University, Montréal, Quebec H4H 1R3, Canada.
Hemant K PaudelFrom The Bloomfield Center for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, and Department of Neurology and Neurosurgery, hemant.paudel@mcgill.ca.
Jewish General Hospital · CAMcGill University · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

The N-methyl-d-aspartate receptor (NMDAR) controls synaptic plasticity and memory function and is one of the major inducers of transcription factor Egr-1 in the hippocampus. However, how Egr-1 mediates the NMDAR signal in neurons has remained unclear. Here, we show that the hippocampus of mice lacking Egr-1 displays electrophysiology properties and ultrastructure that are similar to mice overexpressing PSD-95, a major scaffolding protein of postsynaptic density involved in synapse formation, synaptic plasticity, and synaptic targeting of AMPA receptors (AMPARs), which mediate the vast majority of excitatory transmission in the CNS. We demonstrate that Egr-1 is a transcription repressor of the PSD-95 gene and is recruited to the PSD-95 promoter in response to NMDAR activation. Knockdown of Egr-1 in rat hippocampal primary neurons blocks NMDAR-induced PSD-95 down-regulation and AMPAR endocytosis. Likewise, overexpression of Egr-1 in rat hippocampal primary neurons causes reduction in PSD-95 protein level and promotes AMPAR endocytosis. Our data indicate that Egr-1 is involved in NMDAR-mediated PSD-95 down-regulation and AMPAR endocytosis, a process important in the expression of long term depression.

Indexed as

AnimalsChlorocebus aethiopsCOS CellsDisks Large Homolog 4 ProteinEarly Growth Response Protein 1ElectrophysiologyEndocytosisGuanylate KinasesHippocampusHumansLong-Term Synaptic DepressionMembrane ProteinsMemoryMiceMice, Inbred C57BLMice, KnockoutDisks Large Homolog 4 ProteinDlg4 protein, mouseEarly Growth Response Protein 1Egr1 protein, mouseGuanylate KinasesMembrane ProteinsReceptors, AMPAReceptors, N-Methyl-D-Aspartateearly growth response protein 1 (EGR1)endocytosisneurobiologyPSD95transcription regulationα-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor (AMPA receptor, AMPAR)

Identifiers

PMID26475861
PMCPMC4705959
OpenAlexW2258332806

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.