Evidence map›Paper›PMID 20141542›Full record

ArticleImmunology2010

Lipopolysaccharide induces calcitonin gene-related peptide in the RAW264.7 macrophage cell line.

Weiya Ma, Yvan Dumont, Freya Vercauteren, Remi Quirion

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

37 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
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  11. The diversity of neuroimmune circuits controlling lung inflammation.American journal of physiology. Lung cellular and molecular physiology · 2023
    Review
  12. Review
  13. Dural Immune Cells, CGRP, and Migraine.Frontiers in neurology · 2022
    Review
  14. Review
  15. Review
  16. Article
  17. Biodegradable Magnesium-Based Implants in Orthopedics-A General Review and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Review
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Weiya MaDouglas Mental Health University Institute, McGill University, Montreal, QC, Canada. weiya.ma@douglas.mcgill.ca
Yvan Dumont
Freya Vercauteren
Remi Quirion
Douglas Mental Health University Institute · CAMcGill University · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

summaryCalcitonin gene-related peptide (CGRP) is widely distributed and plays important roles in a wide array of biological functions. It is enriched in primary sensory neurons and hence involved in nociception and neurogenic inflammation. Recent studies have shown that CGRP can be produced by immune cells such as monocytes/macrophages following inflammatory stimulation, suggesting a role in innate immunity. However, it is unclear how CGRP is up-regulated in macrophages and if it plays a role in macrophage functions such as the production of cytokines and chemokines. Using enzyme-linked immunosorbent assay (ELISA) and multiplex ELISA, lipopolysaccharide (LPS) was found to induce CGRP in the RAW 264.7 macrophage cell line. LPS-induced inflammatory mediators such as nerve growth factor (NGF), interleukin-1beta (IL-1beta), IL-6, prostaglandin E(2) (PGE(2)) and nuclear factor-kappaB (NF-kappaB) signalling are involved in inducing CGRP, whereas the NGF receptor trkA and CGRP receptor signalling pathways are unexpectedly involved in suppressing LPS-induced CGRP, which leads to the fine-tune regulation of CGRP release. Exogenous CGRP and CGRP receptor antagonists, in a concentration-dependent manner, stimulated, inhibited or had no effect on basal or LPS-induced release of monocyte chemoattractant protein-1, IL-1beta, IL-6, tumour necrosis factor-alpha and IL-10 in RAW macrophages. The ligand-concentration-dependent regulation of the production of inflammatory mediators by CGRP receptor signalling is a novel mechanism underlying the stimulating and suppressing role of CGRP in immune and inflammatory responses. Together, our data suggest that monocytes/macrophages are an important source of CGRP. Inflammation-induced CGRP has a positive or negative reciprocal effect on the production of other pro- and anti-inflammatory mediators. Thereby CGRP plays both facilitating and suppressing roles in immune and inflammatory responses.

Indexed as

AnimalsAntibodiesCalcitonin Gene-Related PeptideCalcitonin Receptor-Like ProteinCell LineChemokinesCycloheximideCyclooxygenase 2 InhibitorsCytokinesDactinomycinDinoprostoneEnzyme InhibitorsI-kappa B ProteinsInterleukin-1betaInterleukin-6Interleukin-6 Inhibitors3-(4-methylphenylsulfonyl)-2-propenenitrileAntibodiesCalcitonin Gene-Related Peptidecalcitonin gene-related peptide (8-37)Calcitonin Receptor-Like ProteinCalcrl protein, mouseChemokinesCycloheximideCyclooxygenase 2 InhibitorsCytokinesDactinomycinDinoprostoneEnzyme InhibitorsI kappa B beta proteinI-kappa B ProteinsInterleukin-1betaInterleukin-6Interleukin-6 InhibitorsIntracellular Signaling Peptides and ProteinsLipopolysaccharidesMembrane ProteinsN-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamideNerve Growth FactorNitrilesNitrobenzenesolcegepantPeptide FragmentsPiperazinesQuinazolinesReceptor Activity-Modifying ProteinsReceptors, CalcitoninReceptor, trkASulfonamidesSulfonesTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID20141542
PMCPMC2913219
OpenAlexW2098226285

What OpenQuestion holds

Textmetadata
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.