Evidence map›Paper›PMID 34880868›Full record

ArticleFrontiers in immunology2021

Exposure of Microglia to Interleukin-4 Represses NF-κB-Dependent Transcription of Toll-Like Receptor-Induced Cytokines.

Ella A Zuiderwijk-Sick, Céline van der Putten, Raissa Timmerman, Jennifer Veth, Erica M Pasini, Linda van Straalen, Paul van der Valk, Sandra Amor, Jeffrey J Bajramovic

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-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

12 citing papers in PubMed, 22 citations in OpenAlex.

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  7. Alterations of the blood-brain barrier during aging.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Review
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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

9 authors at 2 institutions in 1 country.

Ella A Zuiderwijk-SickAlternatives Unit, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Céline van der PuttenAlternatives Unit, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Raissa TimmermanAlternatives Unit, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Jennifer VethAlternatives Unit, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Erica M PasiniDepartment of Parasitology, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Linda van StraalenAlternatives Unit, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Paul van der ValkDepartment of Pathology, Vrije Universiteit (VU) Medical Centre, Amsterdam, Netherlands.
Sandra AmorDepartment of Pathology, Vrije Universiteit (VU) Medical Centre, Amsterdam, Netherlands.
Jeffrey J BajramovicDepartment of Parasitology, Biomedical Primate Research Centre, Rijswijk, Netherlands.
Biomedical Primate Research Centre · NLVrije Universiteit Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin (IL)-4 is a cytokine that affects both adaptive and innate immune responses. In the central nervous system, microglia express IL-4 receptors and it has been described that IL-4-exposed microglia acquire anti-inflammatory properties. We here demonstrate that IL-4 exposure induces changes in the cell surface protein expression profile of primary rhesus macaque microglia and enhances their potential to induce proliferation of T cells with a regulatory signature. Moreover, we show that Toll like receptor (TLR)-induced cytokine production is broadly impaired in IL-4-exposed microglia at the transcriptional level. IL-4 type 2 receptor-mediated signaling is shown to be crucial for the inhibition of microglial innate immune responses. TLR-induced nuclear translocalization of NF-κB appeared intact, and we found no evidence for epigenetic modulation of target genes. By contrast, nuclear extracts from IL-4-exposed microglia contained significantly less NF-κB capable of binding to its DNA consensus site. Further identification of the molecular mechanisms that underlie the inhibition of TLR-induced responses in IL-4-exposed microglia may aid the design of strategies that aim to modulate innate immune responses in the brain, for example in gliomas.

Indexed as

AnimalsCell ProliferationCells, CulturedCytokinesFemaleHistone DeacetylasesLipopolysaccharidesMacaca mulattaMaleMicrogliaNF-kappa BT-LymphocytesToll-Like ReceptorsTranscription, GeneticCytokinesHistone DeacetylasesLipopolysaccharidesNF-kappa BToll-Like Receptorsalternative activationgliomainnate immunitymacrophagesmicrogliatoll-like receptor

Identifiers

PMID34880868
PMCPMC8645606
OpenAlexW3216480976

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.