Evidence map›Paper›PMID 32350248›Full record

ArticleNature communications2020

MALT-1 mediates IL-17 neural signaling to regulate C. elegans behavior, immunity and longevity.

Sean M Flynn, Changchun Chen, Murat Artan, Stephen Barratt, Alastair Crisp, Geoffrey M Nelson, Sew-Yeu Peak-Chew, Farida Begum, Mark Skehel, Mario de Bono

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 47 citations in OpenAlex.

  1. The neuroimmune system and cognition.Nature immunology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. A structural atlas of death domain fold proteins reveals their versatile roles in biology and function.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Analysis ofComputational and structural biotechnology journal · 2024
    Article
  8. Article
  9. The IL-17 pathway intertwines with neurotrophin and TLR/IL-1R pathways since its domain shuffling origin.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Neuronal IL-17 controlsProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Innate immunity in C. elegans.Current topics in developmental biology · 2021
    Review
  19. IL-17: good fear no tears.Nature immunology · 2020
    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

10 authors at 3 institutions in 4 countries.

Sean M FlynnCell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.ORCID http://orcid.org/0000-0001-7326-2659
Changchun ChenCell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.ORCID http://orcid.org/0000-0003-2233-8996
Murat ArtanCell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.
Stephen BarrattCell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.
Alastair CrispCell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.
Geoffrey M NelsonCell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.ORCID http://orcid.org/0000-0001-9825-4241
Sew-Yeu Peak-ChewBiological Mass Spectrometry and Proteomics, Cell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.
Farida BegumBiological Mass Spectrometry and Proteomics, Cell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.
Mark SkehelBiological Mass Spectrometry and Proteomics, Cell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.
Mario de BonoCell Biology Division, Medical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom. mdebono@ist.ac.at.ORCID http://orcid.org/0000-0001-8347-0443
MRC Laboratory of Molecular Biology · GBHarvard University · USInstitute of Science and Technology Austria · AT

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Medical Research Council MC_U105178786NIH HHS P40 OD010440Wellcome TrustWellcome Trust 209504/Z/17/Z
6 · The paper itself

Abstract

Besides pro-inflammatory roles, the ancient cytokine interleukin-17 (IL-17) modulates neural circuit function. We investigate IL-17 signaling in neurons, and the extent it can alter organismal phenotypes. We combine immunoprecipitation and mass spectrometry to biochemically characterize endogenous signaling complexes that function downstream of IL-17 receptors in C. elegans neurons. We identify the paracaspase MALT-1 as a critical output of the pathway. MALT1 mediates signaling from many immune receptors in mammals, but was not previously implicated in IL-17 signaling or nervous system function. C. elegans MALT-1 forms a complex with homologs of Act1 and IRAK and appears to function both as a scaffold and a protease. MALT-1 is expressed broadly in the C. elegans nervous system, and neuronal IL-17-MALT-1 signaling regulates multiple phenotypes, including escape behavior, associative learning, immunity and longevity. Our data suggest MALT1 has an ancient role modulating neural circuit function downstream of IL-17 to remodel physiology and behavior.

Indexed as

ImmunityLongevityAnimalsBehavior, AnimalCaenorhabditis elegansCaenorhabditis elegans ProteinsGene Expression RegulationGreen Fluorescent ProteinsInterleukin-17InterneuronsModels, BiologicalMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinNeuronsOxygenSignal TransductionSubcellular FractionsCaenorhabditis elegans ProteinsGreen Fluorescent ProteinsInterleukin-17Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinOxygen

Identifiers

PMID32350248
PMCPMC7190641
OpenAlexW3022167651

What OpenQuestion holds

Textmetadata
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.