Cited by 159Cell death mechanisms and regulationImmune Response and Inflammationinterferon and immune responses

An evolutionary perspective on the necroptotic pathway

Dondelinger, Yves, Hulpiau, Paco, Saeys, Yvan, Bertrand, Mathieu J.M., Vandenabeele, Peter·2016·Trends in Cell Biology

Abstract

Throughout the animal kingdom, innate immune receptors protect the organism from microbial intruders by activating pathways that mediate inflammation and pathogen clearance. Necroptosis contributes to the innate immune response by killing pathogen-infected cells and by alerting the immune system through the release of danger signals. Components of the necroptotic signaling axis - TIR-domain-containing adapter-inducing interferon-β (TRIF), Z-DNA sensor DAI, receptor-interacting kinase (RIPK)1, RIPK3 and mixed-lineage kinase domain-like protein (MLKL) - are therefore expected to be found in all animals. However, a phylogenetic analysis reveals that the necroptotic axis, except for RIPK1, is poorly conserved in the animal kingdom, suggesting that alternative mechanisms regulate necroptosis in these species or that necroptosis would apparently be absent. These findings question the universal role of necroptosis during innate immunity in the animal kingdom.

Integrity signals

Registry

Crossref · 10.1016/j.tcb.2016.06.004

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

The citation lists haven’t been fetched yet

References 81 · Cited by 159

Authors
Dondelinger, Y., Hulpiau, P., Saeys, Y., Bertrand, M. J. M., & Vandenabeele, P.
Affiliations
  • Ghent University (BE)
  • Ghent University Hospital (BE)
  • Vlaams Instituut voor Biotechnologie (BE)
Corresponding author
Vandenabeele, Peter
Venue
Trends in Cell Biology
Publisher
Elsevier BV
Published
2016-10
Volume
26
Issue
10
Pages
721-732
ISSN
0962-8924 (ISSN-L)
OpenAlex
W2464409316
Cited by
159
References
81
Citations by year
2026: 16 · 2025: 10 · 2024: 25 · 2023: 16 · 2022: 13 · 2021: 26 · 2020: 17 · 2019: 12 · 2018: 10 · 2017: 10 · 2016: 4
FWCI
1.09
Type
journal article
Language
en
Open access
closed
Locations
  • Trends in Cell Biology (publishedVersion)
  • PubMed (publishedVersion)
  • Ghent University Academic Bibliography (Ghent University) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
  • Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
  • Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
Keywords
necroptosis, innate immunity, phylogenetic conservation, TRIF, DAI, RIPK1, RIPK3, MLKL, damage-associated molecular patterns, pathogen clearance, inflammation
MeSH terms
Animals, Biological Evolution, Humans, Immunity, Innate, Inflammation, Necrosis, Phylogeny, Apoptosis

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review