Evidence map›Paper›PMID 18991139›Full record

ArticleJournal of neurovirology2008

Characterization of retinoic acid-inducible gene-I expression in primary murine glia following exposure to vesicular stomatitis virus.

Samantha R Furr, Vinita S Chauhan, David Sterka, Valery Grdzelishvili, Ian Marriott

Abstract read
In one paragraph

Article in Journal of neurovirology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

42 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
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  7. Immune Functions of Astrocytes in Viral Neuroinfections.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Review
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  11. Article
  12. Review
  13. Article
  14. Review
  15. Cytosolic DNA Sensors and CNS Responses to Viral Pathogens.Frontiers in cellular and infection microbiology · 2020
    Review
  16. Article
  17. Astrocytes: Heterogeneous and Dynamic Phenotypes in Neurodegeneration and Innate Immunity.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2019
    Review
  18. Article
  19. Article
  20. Review
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

5 authors at 1 institution in 1 country.

Samantha R FurrDepartment of Biology, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, USA.
Vinita S Chauhan
David Sterka
Valery Grdzelishvili
Ian Marriott
University of North Carolina at Charlotte · US

Funding

Substance P exacerbation of CNS inflammationR01NS050325 · NINDS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI MARRIOTT, IAN, PHILIPP, MARIO TOMAS · 2006 to 2016
$3.6M
Novel intracellular pattern recognition receptor expression by resident CNS cellsR03NS057434 · NINDS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI MARRIOTT, IAN · 2007 to 2009
$209k
NINDS NIH HHS NS050325NINDS NIH HHS NS057434NINDS NIH HHS R01 NS050325NINDS NIH HHS R03 NS057434
6 · The paper itself

Abstract

Vesicular stomatitis virus (VSV) is a negative-sense single-stranded RNA virus that closely resembles its deadly cousin, rabies virus. In mice, VSV elicits a rapid and severe T cell-independent encephalitis, indicating that resident glial cells play an important role in the initiation of central nervous system (CNS) inflammation. Recently, retinoic acid-inducible gene I (RIG-I)-like helicases have been shown to function as intracellular pattern recognition receptors for replicative viral RNA motifs. In the present study, we demonstrate that the expression of two members of this RIG-I-like receptor family (RLR), RIG-I and melanoma differentiation-associated antigen 5 (MDA5), are elevated in mouse brain tissue following intranasal administration of VSV. Using isolated cultures of primary murine glial cells, we demonstrate that microglia and astrocytes constitutively express both RIG-I and MDA5 transcripts and protein. Importantly, we show that such expression is elevated following challenge with VSV or another negative-sense RNA virus, Sendai virus. The authors provide evidence that such induction is indirect and secondary to the production of soluble mediators by infected cells. Circumstantial evidence for the functional nature of RLR expression in glial cells comes from the observation that microglia express the RLR downstream effector molecule, interferon promoter stimulator-1, and demonstrate diminished levels of the negative RLR regulator, laboratory of genetics and physiology 2, following viral challenge. These findings raise the exciting possibility that RLR molecules play important roles in the detection of viral CNS pathogens and the initiation of protective immune responses or, alternatively, the progression of damaging inflammation within the brain.

Indexed as

VesiculovirusAnimalsCells, CulturedDEAD Box Protein 58DEAD-box RNA HelicasesGene Expression RegulationInterferon-Induced Helicase, IFIH1MiceMice, Inbred C57BLNeurogliaReceptors, VirusRhabdoviridae InfectionsDdx58 protein, mouseDEAD Box Protein 58DEAD-box RNA HelicasesIfih1 protein, mouseInterferon-Induced Helicase, IFIH1Receptors, Virus

Identifiers

PMID18991139
PMCPMC3833003
OpenAlexW2147037014

What OpenQuestion holds

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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.