Evidence map›Paper›PMID 21124967›Full record

ArticlePloS one2010

Effects of the TLR2 agonists MALP-2 and Pam3Cys in isolated mouse lungs.

Martina Barrenschee, Dennis Lex, Stefan Uhlig

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Lipopeptides for Vaccine Development.Bioconjugate chemistry · 2021
    Review
  6. Chemokines and chemokine receptors during COVID-19 infection.Computational and structural biotechnology journal · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Sepsis: in search of cure.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. TLR4 as receptor for HMGB1-mediated acute lung injury after liver ischemia/reperfusion injury.Laboratory investigation; a journal of technical methods and pathology · 2013
    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

3 authors at 2 institutions in 1 country.

Martina BarrenscheeInstitute of Pharmacology and Toxicology, University Hospital Aachen, RWTH Aachen University, Aachen, Germany.
Dennis Lex
Stefan Uhlig
Universitätsklinikum Aachen · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGram-positive and Gram-negative bacteria are main causes of pneumonia or acute lung injury. They are recognized by the innate immune system via toll-like receptor-2 (TLR2) or TLR4, respectively. Among all organs, the lungs have the highest expression of TLR2 receptors, but little is known about the pulmonary consequences of their activation. Here we studied the effects of the TLR2/6 agonist MALP-2, the TLR2/1 agonist Pam(3)Cys and the TLR4 agonist lipopolysaccharide (LPS) on pro-inflammatory responses in isolated lungs. METHODOLOGY/PRINCIPAL

findingsIsolated perfused mouse lungs were perfused for 60 min or 180 min with MALP-2 (25 ng/mL), Pam(3)Cys (160 ng/mL) or LPS (1 µg/mL). We studied mediator release by enzyme linked immunosorbent assay (ELISA), the activation of mitogen activated protein kinase (MAPK) and AKT/protein kinase B by immunoblotting, and gene induction by quantitative polymerase chain reaction. All agonists activated the MAPK ERK1/2 and p38, but neither JNK or AKT kinase. The TLR ligands upregulated the inflammation related genes Tnf, Il1β, Il6, Il10, Il12, Ifng, Cxcl2 (MIP-2α) and Ptgs2. MALP-2 was more potent than Pam(3)Cys in inducing Slpi, Cxcl10 (IP10) and Parg. Remarkable was the strong induction of Tnc by MALP2, which was not seen with Pam(3)Cys or LPS. The growth factor related genes Areg and Hbegf were not affected. In addition, all three TLR agonists stimulated the release of IL-6, TNF, CXCL2 and CXCL10 protein from the lungs. CONCLUSIONS/SIGNIFICANCE: TLR2 and TLR4 activation leads to similar reactions in the lungs regarding MAPK activation, gene induction and mediator release. Several genes studied here have not yet been appreciated as targets of TLR2-activation in the lungs before, i.e., Slpi, tenascin C, Parg and Traf1. In addition, the MALP-2 dependent induction of Tnc may indicate the existence of TLR2/6-specific pathways.

Indexed as

AnimalsChemokine CXCL2Cluster AnalysisCytokinesEnzyme ActivationEnzyme-Linked Immunosorbent AssayFemaleGene ExpressionGene Expression ProfilingImmunoblottingInflammation MediatorsInterferon-gammaInterleukin-1betaIn Vitro TechniquesLipopeptidesLipopolysaccharidesChemokine CXCL2Cxcl2 protein, mouseCytokinesInflammation MediatorsInterferon-gammaInterleukin-1betaLipopeptidesLipopolysaccharidesmacrophage stimulatory lipopeptide 2Mitogen-Activated Protein KinasesPam(3)CSK(4) peptideToll-Like Receptor 2Toll-Like Receptor 4

Identifiers

PMID21124967
PMCPMC2987752
OpenAlexW2086851541

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.