Evidence map›Paper›PMID 18606818›Full record

ArticleThe Journal of biological chemistry2008

SDF1alpha/CXCR4 signaling, via ERKs and the transcription factor Egr1, induces expression of a 67-kDa form of glutamic acid decarboxylase in embryonic hippocampal neurons.

Yongquan Luo, Justin Lathia, Mohammed Mughal, Mark P Mattson

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

38 citing papers in PubMed, 63 citations in OpenAlex.

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  13. Endocytic Trafficking of HIV gp120 is Mediated by Dynamin and Plays a Role in gp120 Neurotoxicity.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2017
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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

4 authors at 1 institution in 1 country.

Yongquan LuoLaboratory of Neurosciences, NIA Intramural Research Program, National Institutes of Health, Baltimore, Maryland 21224, USA.
Justin Lathia
Mohammed Mughal
Mark P Mattson
National Institutes of Health · US

Funding

Stem Cells And NeurogenesisZ01AG000324 · NIA · AGING · PI MATTSON, MARK · 2002 to 2007
$782k
Stem Cells And NeurogenesisZIAAG000324 · NIA · NATIONAL INSTITUTE ON AGING · PI MATTSON, MARK · 2009 to 2014
$585k
Intramural NIH HHS
6 · The paper itself

Abstract

Stromal cell-derived factor alpha (SDF1alpha) and its cognate receptor CXCR4 play an important role in neuronal development in the hippocampus, but the genes directly regulated by SDF1alpha/CXCR4 signaling are unknown. To study the role of CXCR4 targeted genes in neuronal development, we used neuronal cultures established from embryonic day 18 rats. Hippocampal neurons express CXCR4 receptor proteins and are stimulated by SDF1alpha resulting in activation of extracellular signal-regulated kinase (ERK)1/2 and the transcription factor cAMP-response element-binding protein. SDF1alpha rapidly induces the expression of the early growth response gene Egr1, a transcription factor involved in activity-dependent neuronal responses, in a concentration-dependent manner. Gel-shift analysis showed that SDF1alpha enhances DNA binding activity to the Egr1-containing promoter for GAD67. Chromatin immunoprecipitation analysis using an Egr1 antibody indicated that SDF1alpha stimulation increases binding of Egr1 to a GAD67 promoter DNA sequence. SDF1alpha stimulation increases the expression of GAD67 at both the mRNA and protein levels, and increases the amount and neurite localization of gamma-aminobutyric acid (GABA) in neurons already expressing GABA. SDF1alpha-induced Egr1/GAD67 expression is mediated by the G protein-coupled CXCR4 receptor and activation of the ERK pathway. Reduction of Egr1 gene expression using small interfering RNA technology lowers the level of GAD67 transcripts and inhibits SDF1alpha-induced GABA production. Inhibition of CXCR4 activation in the developing mouse brain in utero greatly reduced Egr1 and GAD67 mRNA levels and GAD67 protein levels, suggesting a pivotal role for CXCR4 signaling in the development of GABAergic neurons in vivo. Our data suggest that SDF1alpha/CXCR4/G protein/ERK signaling induces the expression of the GAD67 system via Egr1 activation, a mechanism that may promote the maturation of GABAergic neurons during development.

Indexed as

AnimalsChemokine CXCL12Dose-Response Relationship, DrugEarly Growth Response Protein 1Embryo, MammalianExtracellular Signal-Regulated MAP KinasesFemalegamma-Aminobutyric AcidGene Expression Regulation, DevelopmentalGene Expression Regulation, EnzymologicGlutamate DecarboxylaseHippocampusMAP Kinase Signaling SystemMiceNeuritesPregnancyChemokine CXCL12Cxcl12 protein, mouseCXCR4 protein, mouseCxcr4 protein, ratEarly Growth Response Protein 1Egr1 protein, mouseEgr1 protein, ratExtracellular Signal-Regulated MAP Kinasesgamma-Aminobutyric AcidGlutamate Decarboxylaseglutamate decarboxylase 1Receptors, CXCR4RNA, MessengerRNA, Small Interfering

Identifiers

PMID18606818
PMCPMC2529007
OpenAlexW1980201109

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.