Evidence map›Paper›PMID 24573680›Full record

ArticleThe Journal of biological chemistry2014

Defective chemokine signal integration in leukocytes lacking activator of G protein signaling 3 (AGS3).

Melissa Branham-O'Connor, William G Robichaux, Xian-Kui Zhang, Hyeseon Cho, John H Kehrl, Stephen M Lanier, Joe B Blumer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-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

23 citing papers in PubMed, 29 citations in OpenAlex.

  1. GPSM1 restricts CD73Nature communications · 2026
    Article
  2. Myeloid GPSM1 regulates atherosclerosis progression by governing monocyte and macrophage activation and chemotaxis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
  5. Article
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  7. Article
  8. Article
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  10. Article
  11. AGS3 and GαMolecules (Basel, Switzerland) · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Regulation of Chemokine Signal Integration by Activator of G-Protein Signaling 4 (AGS4).The Journal of pharmacology and experimental therapeutics · 2017
    Article
  17. Review
  18. Article
  19. Article
  20. Article
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

7 authors at 3 institutions in 1 country.

Melissa Branham-O'ConnorDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina 29425.
William G RobichauxDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina 29425.
Xian-Kui ZhangDepartment of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, South Carolina 29425.
Hyeseon ChoB-cell Section, NIAID, National Institutes of Health, Bethesda, Maryland 20892.
John H KehrlB-cell Section, NIAID, National Institutes of Health, Bethesda, Maryland 20892.
Stephen M LanierDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina 29425.
Joe B BlumerDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, South Carolina 29425. Electronic address: blumerjb@musc.edu.
Medical University of South Carolina · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

South Carolina IDeA Networks of Biomedical Research (SC INBRE V)P20GM103499 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI EDIE C GOLDSMITH · 2012 to 2026
$61.0M
Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
Control Of G Protein Signaling: Role Of The RGSsZIAAI000738 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KEHRL, JOHN H · 2009 to 2025
$15.9M
Analysis of the Functional Roles of a Novel G-alpha Nucleotide CycleZIAAI000961 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KEHRL, JOHN H · 2009 to 2018
$4.4M
MUSC FACIL EXPANSION &RENOV: SLE C06RR015455 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CROUCH, ROSALIE K · 2002 to 2002
$2.0M
ACCESSORY PROTEINS AND G-PROTEIN SIGNALING MECHANISMSR01DA025896 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LANIER, STEPHEN M. · 2008 to 2012
$1.6M
AGS4 in G-protein Signal ProcessingR01GM086510 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BLUMER, JOE B · 2009 to 2013
$1.5M
Molecular mechanisms of the impact of Fli-1 on lupusR01AR056670 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ZHANG, XIAN · 2010 to 2014
$1.4M
TRAINING IN CANCER THERAPEUTICST32CA119945 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI TEW, KENNETH D. · 2006 to 2010
$1.3M
Fluorometric Imaging Plate Reader (FLIPRtetra)S10RR027777 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LUTTRELL, LOUIS M · 2010 to 2010
$500k
Intramural NIH HHSNCI NIH HHS P30 CA138313NCI NIH HHS T32 CA119945NCI NIH HHS T32CA119945NCRR NIH HHS C06 RR015455NCRR NIH HHS S10 RR027777NIAMS NIH HHS AR056670NIAMS NIH HHS R01 AR056670NIDA NIH HHS DA025896NIDA NIH HHS R01 DA025896NIGMS NIH HHS GM086510NIGMS NIH HHS P20 GM103499NIGMS NIH HHS P20GM103499NIGMS NIH HHS R01 GM086510NIMHD NIH HHS L60 MD003100
6 · The paper itself

Abstract

Activator of G-protein signaling 3 (AGS3, gene name G-protein signaling modulator-1, Gpsm1), an accessory protein for G-protein signaling, has functional roles in the kidney and CNS. Here we show that AGS3 is expressed in spleen, thymus, and bone marrow-derived dendritic cells, and is up-regulated upon leukocyte activation. We explored the role of AGS3 in immune cell function by characterizing chemokine receptor signaling in leukocytes from mice lacking AGS3. No obvious differences in lymphocyte subsets were observed. Interestingly, however, AGS3-null B and T lymphocytes and bone marrow-derived dendritic cells exhibited significant chemotactic defects as well as reductions in chemokine-stimulated calcium mobilization and altered ERK and Akt activation. These studies indicate a role for AGS3 in the regulation of G-protein signaling in the immune system, providing unexpected venues for the potential development of therapeutic agents that modulate immune function by targeting these regulatory mechanisms.

Indexed as

Signal TransductionAmino Acid MotifsAnimalsB-LymphocytesBone Marrow CellsCalciumCarrier ProteinsChemokinesChemotaxisDendritic CellsFemaleGTP-Binding ProteinsGuanine Nucleotide Dissociation InhibitorsImmune SystemLeukocytesMaleCalciumCarrier ProteinsChemokinesGpsm1 protein, mouseGTP-Binding ProteinsGuanine Nucleotide Dissociation InhibitorsAGS3ChemokinesChemotaxisCxcr4GPR MotifG-protein-coupled Receptors (GPCR)G ProteinsGpsm1GαiGβγ

Identifiers

PMID24573680
PMCPMC4036190
OpenAlexW2017990834

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.