Evidence map›Paper›PMID 35793229›Full record

ArticleeLife2022

The transcription factor RUNX2 drives the generation of human NK cells and promotes tissue residency.

Sigrid Wahlen, Filip Matthijssens, Wouter Van Loocke, Sylvie Taveirne, Laura Kiekens, Eva Persyn, Els Van Ammel, Zenzi De Vos, Stijn De Munter, Patrick Matthys and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.6field-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

24 citing papers in PubMed, 33 citations in OpenAlex.

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  13. Restriction of innate Tγδ17 cell plasticity by an AP-1 regulatory axis.bioRxiv : the preprint server for biology · 2024
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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

15 authors at 2 institutions in 1 country.

Sigrid WahlenDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.ORCID 0000-0003-2606-1023
Filip MatthijssensCancer Research Institute Ghent, Ghent, Belgium.
Wouter Van LoockeCancer Research Institute Ghent, Ghent, Belgium.
Sylvie TaveirneDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Laura KiekensDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Eva PersynDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Els Van AmmelDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Zenzi De VosDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Stijn De MunterDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.ORCID 0000-0003-3821-0620
Patrick MatthysLaboratory of Immunobiology, Rega Institute for Medical Research, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.ORCID 0000-0002-9685-6836
Filip Van NieuwerburghDepartment of Pharmaceutics, Ghent University, Ghent, Belgium.
Tom TaghonDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.ORCID 0000-0002-5781-0288
Bart VandekerckhoveDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Pieter Van VlierbergheCancer Research Institute Ghent, Ghent, Belgium.ORCID 0000-0001-9063-7205
Georges LeclercqDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.ORCID 0000-0002-1691-5294
Ghent University · BERega Institute for Medical Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells are innate lymphocytes that eliminate virus-infected and cancer cells by cytotoxicity and cytokine secretion. In addition to circulating NK cells, distinct tissue-resident NK subsets have been identified in various organs. Although transcription factors regulating NK cell development and function have been extensively studied in mice, the role of RUNX2 in these processes has not been investigated, neither in mice nor in human. Here, by manipulating RUNX2 expression with either knockdown or overexpression in human haematopoietic stem cell-based NK cell differentiation cultures, combined with transcriptomic and ChIP-sequencing analyses, we established that RUNX2 drives the generation of NK cells, possibly through induction of IL-2Rβ expression in NK progenitor cells. Importantly, RUNX2 promotes tissue residency in human NK cells. Our findings have the potential to improve existing NK cell-based cancer therapies and can impact research fields beyond NK cell biology, since tissue-resident subsets have also been described in other lymphocyte subpopulations.

Indexed as

Transcription FactorsCore Binding Factor Alpha 1 SubunitGene Expression RegulationHumansKiller Cells, NaturalCore Binding Factor Alpha 1 SubunitRUNX2 protein, humanTranscription FactorshumanimmunologyinflammationmouseNK cell developmentRUNX2tissue residency

Identifiers

PMID35793229
PMCPMC9259014
OpenAlexW4284709635

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.