Evidence map›Paper›PMID 23935652›Full record

ReviewClinical & developmental immunology2013

Inflammatory chemokine expression via Toll-like receptor 3 signaling in normal human mesangial cells.

Hiroshi Tanaka, Tadaatsu Imaizumi

Open access · goldAbstract readReview
In one paragraph

Review in Clinical & developmental immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. ST32da, a NovelCells · 2025
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  9. Botanically-Derived ΔMolecules (Basel, Switzerland) · 2022
    Article
  10. Mesangial Cells in Lupus Nephritis.Current rheumatology reports · 2022
    Review
  11. Article
  12. Mesangial cell: A hub in lupus nephritis.Frontiers in immunology · 2022
    Review
  13. Article
  14. Article
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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

2 authors at 1 institution in 1 country.

Hiroshi TanakaDepartment of School Health Science, Hirosaki University Faculty of Education, 1 Bunkyo-cho, Hirosaki 036-8560, Japan. hirotana@cc.hirosaki-u.ac.jp
Tadaatsu Imaizumi
Hirosaki University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate and adaptive immune systems have been reported to play an important role in the pathogenesis of glomerular diseases. Since viral infections may trigger the development of inflammatory renal disease or the worsening of preexisting renal disease, recent studies have focused on the involvement of toll-like receptors (TLRs) and their signaling pathways in the inflammatory processes of glomerular cells. Viral double-stranded RNA (dsRNA) can activate not only TLR3 located within intracellular endosomes but also retinoic-acid-inducible-gene-I- (RIG-I-) like helicase receptors located within the cytosol. RIG-I and melanoma differentiation-associated gene 5 (MDA5) are members of the RNA helicase family in the cytosol, and both act as pathogen recognition receptors. The activation of TLRs and their downstream immune responses can be induced by both infectious pathogens and noninfectious stimuli such as endogenous ligands, and this mechanism may be involved in the pathogenesis of autoimmune renal diseases. However, there are few data on the interaction between TLR3, MDA5, and RIG-I in autoimmune glomerular diseases. Based on our recent experimental studies using cultured normal human mesangial cells (MCs), we found that novel TLR3-mediated signaling pathways in MCs may be involved in the pathogenesis of glomerular diseases. In the present paper, we summarize our recent findings.

Indexed as

Adaptor Proteins, Signal TransducingChemokinesDEAD Box Protein 58DEAD-box RNA HelicasesGene Expression RegulationHumansInflammation MediatorsMesangial CellsProtein BindingReceptors, ImmunologicRNA-Binding ProteinsSignal TransductionSmad5 ProteinToll-Like Receptor 3Transcription FactorsAdaptor Proteins, Signal TransducingChemokinesDEAD Box Protein 58DEAD-box RNA HelicasesIFIT1 protein, humanInflammation MediatorsReceptors, ImmunologicRIGI protein, humanRNA-Binding ProteinsSmad5 ProteinToll-Like Receptor 3Transcription Factors

Identifiers

PMID23935652
PMCPMC3710592
OpenAlexW2160019745

What OpenQuestion holds

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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.