Evidence map›Paper›PMID 21167054›Full record

ArticleJournal of neuroinflammation2010

Fractalkine receptor (CX3CR1) deficiency sensitizes mice to the behavioral changes induced by lipopolysaccharide.

Angela W Corona, Yan Huang, Jason C O'Connor, Robert Dantzer, Keith W Kelley, Phillip G Popovich, Jonathan P Godbout

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed, 2 pooled it
7.7field-weighted citation impact, top 3% 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

112 citing papers in PubMed, 2 syntheses or guidelines pooled it, 206 citations in OpenAlex.

  1. What Animal Models Can Tell Us About Long-Term Psychiatric Symptoms in Sepsis Survivors: a Systematic Review.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
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  12. Cortical microglia dynamics are conserved during voluntary wheel running.Journal of applied physiology (Bethesda, Md. : 1985) · 2024
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  13. Article
  14. Alpha-1 antitrypsin inhibits fractalkine-mediated monocyte-lung endothelial cell interactions.American journal of physiology. Lung cellular and molecular physiology · 2023
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  15. P2YThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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52 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

7 authors at 3 institutions in 1 country.

Angela W CoronaDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, 333 W. 10th Ave., Columbus, OH 43210, USA. Angela.Wynne@osumc.edu
Yan Huang
Jason C O'Connor
Robert Dantzer
Keith W Kelley
Phillip G Popovich
Jonathan P Godbout
University of Illinois Urbana-Champaign · USInstitute for Behavioral Medicine · USThe Ohio State University · US

Funding

Neuroimmune Mechanisms of Depressive-Like Behavior During AgingR01AG029573 · NIA · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI KELLEY, KEITH W · 2007 to 2011
$2.1M
AIDS, Immune Activation and Mental HealthR01MH079829 · NIMH · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI DANTZER, ROBERT · 2006 to 2010
$1.8M
Aging, Microglial Dysregulation and DepressionR01AG033028 · NIA · OHIO STATE UNIVERSITY · PI GODBOUT, JONATHAN P · 2009 to 2013
$1.5M
NIA NIH HHS R01 AG 029573NIA NIH HHS R01 AG029573NIA NIH HHS R01-AG-033028NIMH NIH HHS R01 MH 079829
6 · The paper itself

Abstract

backgroundInteractions between fractalkine (CX3CL1) and fractalkine receptor (CX3CR1) regulate microglial activation in the CNS. Recent findings indicate that age-associated impairments in CX3CL1 and CX3CR1 are directly associated with exaggerated microglial activation and an impaired recovery from sickness behavior after peripheral injection of lipopolysaccharide (LPS). Therefore, the purpose of this study was to determine the extent to which an acute LPS injection causes amplified and prolonged microglial activation and behavioral deficits in CX3CR1-deficient mice (CX3CR1-/-).

methodsCX3CR1-/- mice or control heterozygote mice (CX3CR1+/-) were injected with LPS (0.5 mg/kg i.p.) or saline and behavior (i.e., sickness and depression-like behavior), microglial activation, and markers of tryptophan metabolism were determined. All data were analyzed using Statistical Analysis Systems General Linear Model procedures and were subjected to one-, two-, or three-way ANOVA to determine significant main effects and interactions.

resultsLPS injection caused a prolonged duration of social withdrawal in CX3CR1-/- mice compared to control mice. This extended social withdrawal was associated with enhanced mRNA expression of IL-1β, indolamine 2,3-dioxygenase (IDO) and kynurenine monooxygenase (KMO) in microglia 4 h after LPS. Moreover, elevated expression of IL-1β and CD14 was still detected in microglia of CX3CR1-/- mice 24 h after LPS. There was also increased turnover of tryptophan, serotonin, and dopamine in the brain 24 h after LPS, but these increases were independent of CX3CR1 expression. When submitted to the tail suspension test 48 and 72 h after LPS, an increased duration of immobility was evident only in CX3CR1-/- mice. This depression-like behavior in CX3CR1-/- mice was associated with a persistent activated microglial phenotype in the hippocampus and prefrontal cortex.

conclusionsTaken together, these data indicate that a deficiency of CX3CR1 is permissive to protracted microglial activation and prolonged behavioral alterations in response to transient activation of the innate immune system.

Indexed as

AnimalsBehavior, AnimalChemokine CX3CL1CX3C Chemokine Receptor 1DepressionHumansImmunity, InnateInterleukin-1betaLipopolysaccharidesMiceMice, Inbred C57BLMice, KnockoutMicrogliaMotor ActivityOxygenasesReceptors, ChemokineChemokine CX3CL1CX3C Chemokine Receptor 1Cx3cr1 protein, mouseInterleukin-1betaLipopolysaccharidesOxygenasesReceptors, ChemokineTryptophan

Identifiers

PMID21167054
PMCPMC3018416
OpenAlexW2127278809

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.