Evidence map›Paper›PMID 29590608›Full record

ArticleCell reports2018

The Murine Natural Cytotoxic Receptor NKp46/NCR1 Controls TRAIL Protein Expression in NK Cells and ILC1s.

Sam Sheppard, Iona S Schuster, Christopher E Andoniou, Clement Cocita, Thomas Adejumo, Sam K P Kung, Joseph C Sun, Mariapia A Degli-Esposti, Nadia Guerra

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  16. Unleashing the power of NK cells in anticancer immunotherapy.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  17. Article
  18. Review
  19. Innate lymphoid cells type 3 in cancer.Frontiers in immunology · 2022
    Review
  20. Plasticity of Innate Lymphoid Cells in Cancer.Frontiers in immunology · 2022
    Review
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 6 institutions in 4 countries.

Sam SheppardDepartment of Life Sciences, Imperial College London, London SW7 2AZ, UK; Memorial Sloan Kettering Cancer Center, Zuckerman Research Center, 408 East 69th Street, New York, NY 10065, USA.
Iona S SchusterImmunology and Virology Program, Centre for Ophthalmology and Visual Science, The University of Western Australia, Crawley, Western Australia, Australia; Centre for Experimental Immunology, Lions Eye Institute, Nedlands, Western Australia, Australia.
Christopher E AndoniouImmunology and Virology Program, Centre for Ophthalmology and Visual Science, The University of Western Australia, Crawley, Western Australia, Australia; Centre for Experimental Immunology, Lions Eye Institute, Nedlands, Western Australia, Australia.
Clement CocitaDepartment of Life Sciences, Imperial College London, London SW7 2AZ, UK.
Thomas AdejumoMedical Research Center, Hammersmith Hospital, London W12 0NN, UK.
Sam K P KungDepartment of Immunology, Max Rady College of Medicine, University of Manitoba, Winnipeg R3E 0T5, Manitoba, Canada.
Joseph C SunMemorial Sloan Kettering Cancer Center, Zuckerman Research Center, 408 East 69th Street, New York, NY 10065, USA.
Mariapia A Degli-EspostiImmunology and Virology Program, Centre for Ophthalmology and Visual Science, The University of Western Australia, Crawley, Western Australia, Australia; Centre for Experimental Immunology, Lions Eye Institute, Nedlands, Western Australia, Australia.
Nadia GuerraDepartment of Life Sciences, Imperial College London, London SW7 2AZ, UK. Electronic address: n.guerra@imperial.ac.uk.
Imperial College London · GBUniversity of Western Australia · AUHammersmith Hospital · GBLions Eye Institute · AUMemorial Sloan Kettering Cancer Center · USUniversity of Manitoba · CA

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Biotechnology and Biological Sciences Research CouncilNCI NIH HHS P30 CA008748Wellcome Trust 088381/Z/09/A
6 · The paper itself

Abstract

TRAIL is an apoptosis-inducing ligand constitutively expressed on liver-resident type 1 innate lymphoid cells (ILC1s) and a subset of natural killer (NK) cells, where it contributes to NK cell anti-tumor, anti-viral, and immunoregulatory functions. However, the intrinsic pathways involved in TRAIL expression in ILCs remain unclear. Here, we demonstrate that the murine natural cytotoxic receptor mNKp46/NCR1, expressed on ILC1s and NK cells, controls TRAIL protein expression. Using NKp46-deficient mice, we show that ILC1s lack constitutive expression of TRAIL protein and that NK cells activated in vitro and in vivo fail to upregulate cell surface TRAIL in the absence of NKp46. We show that NKp46 regulates TRAIL expression in a dose-dependent manner and that the reintroduction of NKp46 in mature NK cells deficient for NKp46 is sufficient to restore TRAIL surface expression. These studies uncover a link between NKp46 and TRAIL expression in ILCs with potential implications in pathologies involving NKp46-expressing cells.

Indexed as

AnimalsAntigens, LyKiller Cells, NaturalLiverLymphocytesMiceMice, TransgenicNatural Cytotoxicity Triggering Receptor 1TNF-Related Apoptosis-Inducing LigandUp-RegulationAntigens, LyNatural Cytotoxicity Triggering Receptor 1Ncr1 protein, mouseTNF-Related Apoptosis-Inducing LigandTnfsf10 protein, mouseIL-15IL-2ILC1natural killer cellNK cellNKp46TRAIL

Identifiers

PMID29590608
PMCPMC5896200
OpenAlexW2795113333

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.