Evidence map›Paper›PMID 31444264›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Activation Receptor-Dependent IFN-γ Production by NK Cells Is Controlled by Transcription, Translation, and the Proteasome.

Sytse J Piersma, Melissa A Pak-Wittel, Andrea Lin, Beatrice Plougastel-Douglas, Wayne M Yokoyama

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

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  16. RNA Flow Cytometry for the Study of T Cell Metabolism.International journal of molecular sciences · 2021
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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

5 authors at 1 institution in 1 country.

Sytse J PiersmaDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110 spiersma@wustl.edu.ORCID 0000-0002-5379-3556
Melissa A Pak-WittelDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Andrea LinDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0001-5228-8489
Beatrice Plougastel-DouglasDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0002-6389-561X
Wayne M YokoyamaDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0002-0566-7264
Washington University in St. Louis · US

Funding

NATURAL KILLER CELL CONTROL OF MURINE CYTOMEGALOVIRUS INFECTIONR01AI131680 · NIAID · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 2017 to 2025
$6.0M
NIAID NIH HHS R01 AI131680
6 · The paper itself

Abstract

NK cells can recognize target cells such as virus-infected and tumor cells through integration of activation and inhibitory receptors. Recognition by NK cells can lead to direct lysis of the target cell and production of the signature cytokine IFN-γ. However, it is unclear whether stimulation through activation receptors alone is sufficient for IFN-γ production. In this study, we show that NK activation receptor engagement requires additional signals for optimal IFN-γ production, which could be provided by IFN-β or IL-12. Stimulation of murine NK cells with soluble Abs directed against NK1.1, Ly49H, Ly49D, or NKp46 required additional stimulation with cytokines, indicating that a range of activation receptors with distinct adaptor molecules require additional stimulation for IFN-γ production. The requirement for multiple signals extends to stimulation with primary m157-transgenic target cells, which triggers the activation receptor Ly49H, suggesting that NK cells do require multiple signals for IFN-γ production in the context of target cell recognition. Using quantitative PCR and RNA flow cytometry, we found that cytokines, not activating ligands, act on NK cells to express

Indexed as

AnimalsAntigens, LyInterferon-gammaKiller Cells, NaturalMiceMice, KnockoutNatural Cytotoxicity Triggering Receptor 1NK Cell Lectin-Like Receptor Subfamily ANK Cell Lectin-Like Receptor Subfamily BProteasome Endopeptidase ComplexProtein BiosynthesisSignal TransductionTranscription, GeneticAntigens, LyIFNG protein, mouseInterferon-gammaKlra4 protein, mouseKlra8 protein, mouseKlrb1c protein, mouseNatural Cytotoxicity Triggering Receptor 1Ncr1 protein, mouseNK Cell Lectin-Like Receptor Subfamily ANK Cell Lectin-Like Receptor Subfamily BProteasome Endopeptidase Complex

Identifiers

PMID31444264
PMCPMC6760998
OpenAlexW2969903696

What OpenQuestion holds

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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.