Evidence map›Paper›PMID 37352687›Full record

ArticleJournal of neuroimmunology2023

Ablation of microglia following infection of the central nervous system with a neurotropic murine coronavirus infection leads to increased demyelination and impaired remyelination.

Yuting Cheng, Dominic Ibarra Javonillo, Collin Pachow, Vanessa M Scarfone, Kellie Fernandez, Craig M Walsh, Kim N Green, Thomas E Lane

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroimmunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Yuting ChengDepartment of Molecular Biology & Biochemistry, School of Biological Sciences, University of California, Irvine 92697, USA.
Dominic Ibarra JavonilloDepartment of Neurobiology & Behavior, School of Biological Sciences, University of California, Irvine 92697, USA.
Collin PachowDepartment of Molecular Biology & Biochemistry, School of Biological Sciences, University of California, Irvine 92697, USA.
Vanessa M ScarfoneSue & Bill Gross Stem Cell Research Center, University of California, Irvine 92697, USA.
Kellie FernandezDepartment of Neurobiology & Behavior, School of Biological Sciences, University of California, Irvine 92697, USA.
Craig M WalshDepartment of Molecular Biology & Biochemistry, School of Biological Sciences, University of California, Irvine 92697, USA.
Kim N GreenDepartment of Neurobiology & Behavior, School of Biological Sciences, University of California, Irvine 92697, USA.
Thomas E LaneDepartment of Molecular Biology & Biochemistry, School of Biological Sciences, University of California, Irvine 92697, USA; Department of Neurobiology & Behavior, School of Biological Sciences, University of California, Irvine 92697, USA; Center for Virus Research, University of California, Irvine 92697, USA. Electronic address: tlane@uci.edu.
University of California, Irvine · US

Funding

Origins, properties, and therapeutic potential of cells that repopulate the microglia-depleted adult brainR01NS083801 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Kim Green · 2014 to 2026
$5.6M
Defining mechanisms of disease and repair in a viral model of multiple sclerosisR35NS116835 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Thomas E Lane · 2020 to 2026
$5.0M
Endogenous human antibodies in aging and Alzheimer's disease and the immune response to amyloidRF1AG061857 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI GLABE, CHARLES G., WALSH, CRAIG MICHAEL · 2018 to 2018
$3.5M
Microglia are necessary for cortical plaque formation in Alzheimer's diseaseRF1AG056768 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI GREEN, KIM · 2018 to 2018
$2.7M
Examining the role of adaptive immunity in Alzheimer's Disease pathogenesisRF1AG055524 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI BLURTON-JONES, MATHEW MARK · 2017 to 2017
$2.7M
Cellular and Molecular Mechanisms of Regulatory T Cells in EAER01AI121945 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAHALAN, MICHAEL D · 2016 to 2020
$2.5M
The lipid amidase NAAA as a therapeutic target for Alzheimer's diseaseRF1AG065329 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI GREEN, KIM, PIOMELLI, DANIELE · 2020 to 2020
$2.3M
NIAID NIH HHS R01 AI121945NIA NIH HHS RF1 AG055524NIA NIH HHS RF1 AG056768NIA NIH HHS RF1 AG061857NIA NIH HHS RF1 AG065329NINDS NIH HHS R01 NS083801NINDS NIH HHS R35 NS116835
6 · The paper itself

Abstract

Intracranial inoculation of susceptible mice with a glial-tropic strain of mouse hepatitis virus (JHMV), a murine coronavirus, results in an acute encephalomyelitis followed by viral persistence in white matter tracts accompanied by chronic neuroinflammation and demyelination. Microglia are the resident immune cell of the central nervous system (CNS) and are considered important in regulating events associated with neuroinflammation as well as influencing both white matter damage and remyelination. To better understand mechanisms by which microglia contribute to these immune-mediated events, JHMV-infected mice with established demyelination were treated with the small molecular inhibitor of colony stimulating factor 1 receptor (CSF1R), PLX5622, to deplete microglia. Treatment with PLX5622 did not affect viral replication within the CNS yet the severity of demyelination was increased and remyelination impaired compared to control mice. Gene expression analysis revealed that targeting microglia resulted in altered expression of genes associated with immune cell activation and phagocytosis of myelin debris. These findings indicate that microglia are not critical in viral surveillance in persistently JHMV-infected mice yet restrict white matter damage and remyelination, in part, by influencing phagocytosis of myelin debris.

Indexed as

Coronavirus InfectionsDemyelinating DiseasesMurine hepatitis virusRemyelinationWhite MatterAnimalsMiceMice, Inbred C57BLMicrogliaNeuroinflammatory DiseasesOrganic ChemicalsOrganic ChemicalsPLX5622CoronavirusDemyelinationMicrogliaNeuroinflammationRemyelination

Identifiers

PMID37352687
PMCPMC11840753
OpenAlexW4380884677

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.