Evidence map›Paper›PMID 34297254›Full record

ArticleCellular and molecular neurobiology2022

Differential Effects of Toll-Like Receptor Activation and Differential Mediation by MAP Kinases of Immune Responses in Microglial Cells.

Jaedeok Kwon, Christos Arsenis, Maria Suessmilch, Alison McColl, Jonathan Cavanagh, Brian J Morris

Abstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Platelets as central hubs of inflammation.Frontiers in immunology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Downregulation of SF3B2 protects CNS neurons in models of multiple sclerosis.Annals of clinical and translational neurology · 2023
    Article
  12. Article
  13. Article
  14. 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

6 authors.

Jaedeok KwonInstitute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, West Medical Building, Glasgow, G12 8QQ, UK.
Christos ArsenisInstitute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, West Medical Building, Glasgow, G12 8QQ, UK.
Maria SuessmilchInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Alison McCollInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Jonathan Cavanagh *Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Brian J Morris *Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, West Medical Building, Glasgow, G12 8QQ, UK. Brian.Morris@glasgow.ac.uk.ORCID http://orcid.org/0000-0003-4439-0795

Funding

Wellcome TrustWellcome Trust 104025/Z/14/Z
6 · The paper itself

Abstract

Microglial activation is believed to play a role in many psychiatric and neurodegenerative diseases. Based largely on evidence from other cell types, it is widely thought that MAP kinase (ERK, JNK and p38) signalling pathways contribute strongly to microglial activation following immune stimuli acting on toll-like receptor (TLR) 3 or TLR4. We report here that exposure of SimA9 mouse microglial cell line to immune mimetics stimulating TLR4 (lipopolysaccharide-LPS) or TLR7/8 (resiquimod/R848), results in marked MAP kinase activation, followed by induction of nitric oxide synthase, and various cytokines/chemokines. However, in contrast to TLR4 or TLR7/8 stimulation, very few effects of TLR3 stimulation by poly-inosine/cytidine (polyI:C) were detected. Induction of chemokines/cytokines at the mRNA level by LPS and resiquimod were, in general, only marginally affected by MAP kinase inhibition, and expression of TNF, Ccl2 and Ccl5 mRNAs, along with nitrite production, were enhanced by p38 inhibition in a stimulus-specific manner. Selective JNK inhibition enhanced Ccl2 and Ccl5 release. Many distinct responses to stimulation of TLR4 and TLR7 were observed, with JNK mediating TNF protein induction by the latter but not the former, and suppressing Ccl5 release by the former but not the latter. These data reveal complex modulation by MAP kinases of microglial responses to immune challenge, including a dampening of some responses. They demonstrate that abnormal levels of JNK or p38 signalling in microglial cells will perturb their profile of cytokine and chemokine release, potentially contributing to abnormal inflammatory patterns in CNS disease states.

Indexed as

MicrogliaToll-Like Receptor 3AnimalsChemokinesCytidineCytokinesImmunityInosineJNK Mitogen-Activated Protein KinasesLipopolysaccharidesMiceMitogen-Activated Protein KinasesNitritesRNA, MessengerToll-Like Receptor 4Toll-Like Receptor 7ChemokinesCytidineCytokinesInosineJNK Mitogen-Activated Protein KinasesLipopolysaccharidesMitogen-Activated Protein KinasesNitritesRNA, MessengerToll-Like Receptor 3Toll-Like Receptor 4Toll-Like Receptor 7Toll-Like ReceptorsBacterial infectionChemokinesCytokinesMicrogliaPoly (IC)Signaling PathwayViral infection

Identifiers

PMID34297254
PMCPMC9560989

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Registered trials

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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.