Evidence map›Paper›PMID 24516120›Full record

ArticleThe Journal of experimental medicine2014

T-bet and Eomes instruct the development of two distinct natural killer cell lineages in the liver and in the bone marrow.

Cécile Daussy, Fabrice Faure, Katia Mayol, Sébastien Viel, Georg Gasteiger, Emily Charrier, Jacques Bienvenu, Thomas Henry, Emilie Debien, Uzma A Hasan and 7 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 320 papers.

0numbers the graph read from it
0cells of the map it votes in
320citing papers in PubMed
23.7field-weighted citation impact, top 1% 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

320 citing papers in PubMed, 526 citations in OpenAlex.

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  7. Developmental determinants of male bias in medulloblastoma.bioRxiv : the preprint server for biology · 2026
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260 more citing papers are in PubMed but not listed here.

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

17 authors at 9 institutions in 6 countries.

Cécile DaussyCIRI, International Center for Infectiology Research, Université de Lyon; 2 Institut National de la Santé et de la Recherche Médicale, U1111; 3 Ecole Normale Supérieure de Lyon; 4 Université Lyon 1, Centre International de Recherche en Infectiologie; and 5 Centre National de la Recherche Scientifique, UMR5308, 69007 Lyon, France.
Fabrice Faure
Katia Mayol
Sébastien Viel
Georg Gasteiger
Emily Charrier
Jacques Bienvenu
Thomas Henry
Emilie Debien
Uzma A Hasan
Jacqueline Marvel
Keigyou Yoh
Satoru Takahashi
Immo Prinz
Simon de Bernard
Laurent Buffat
Thierry Walzer
Centre National pour la Recherche Scientifique et Technique (CNRST) · MACentre International de Recherche en Infectiologie · FRÉcole Normale Supérieure de Lyon · FRUniversité Claude Bernard Lyon 1 · FRUniversity of Tsukuba · JPInserm · FRInstitut National de Recherche en Santé Publique · MLMedizinische Hochschule Hannover · DEMemorial Sloan Kettering Cancer Center · US

Funding

European Research Council 281025
6 · The paper itself

Abstract

Trail(+)DX5(-)Eomes(-) natural killer (NK) cells arise in the mouse fetal liver and persist in the adult liver. Their relationships with Trail(-)DX5(+) NK cells remain controversial. We generated a novel Eomes-GFP reporter murine model to address this question. We found that Eomes(-) NK cells are not precursors of classical Eomes(+) NK cells but rather constitute a distinct lineage of innate lymphoid cells. Eomes(-) NK cells are strictly dependent on both T-bet and IL-15, similarly to NKT cells. We observed that, in the liver, expression of T-bet in progenitors represses Eomes expression and the development of Eomes(+) NK cells. Reciprocally, the bone marrow (BM) microenvironment restricts T-bet expression in developing NK cells. Ectopic expression of T-bet forces the development of Eomes(-) NK cells, demonstrating that repression of T-bet is essential for the development of Eomes(+) NK cells. Gene profile analyses show that Eomes(-) NK cells share part of their transcriptional program with NKT cells, including genes involved in liver homing and NK cell receptors. Moreover, Eomes(-) NK cells produce a broad range of cytokines, including IL-2 and TNF in vitro and in vivo, during immune responses against vaccinia virus. Thus, mutually exclusive expression of T-bet and Eomes drives the development of different NK cell lineages with complementary functions.

Indexed as

Adoptive TransferAnimalsBone MarrowCell DifferentiationCell LineageDNA PrimersFlow CytometryGene Knock-In TechniquesKiller Cells, NaturalLiverMiceMicroarray AnalysisModels, AnimalReal-Time Polymerase Chain ReactionStem Cell NicheT-bet Transcription FactorDNA PrimersEomes protein, mouseT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID24516120
PMCPMC3949572
OpenAlexW2168405751

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.