Evidence map›Paper›PMID 27069114›Full record

ArticleThe Journal of experimental medicine2016

The ETS1 transcription factor is required for the development and cytokine-induced expansion of ILC2.

Erin C Zook, Kevin Ramirez, Xiaohuan Guo, Grant van der Voort, Mikael Sigvardsson, Eric C Svensson, Yang-Xin Fu, Barbara L Kee

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 89 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Erin C ZookCommittee on Immunology, The University of Chicago, Chicago, IL 60637.
Kevin RamirezCommittee on Immunology, The University of Chicago, Chicago, IL 60637.
Xiaohuan GuoCommittee on Immunology, The University of Chicago, Chicago, IL 60637.
Grant van der VoortDepartment of Pathology, The University of Chicago, Chicago, IL 60637.
Mikael SigvardssonExperimental Hematopoiesis Unit, Department of Clinical and Experimental Medicine, Faculty of Medicine for Health Sciences, Linköping University, 58183 Linköping, Sweden.
Eric C SvenssonDepartment of Medicine, Section of Cardiology, The University of Chicago, Chicago, IL 60637.
Yang-Xin FuCommittee on Immunology, The University of Chicago, Chicago, IL 60637 Department of Pathology, The University of Chicago, Chicago, IL 60637.
Barbara L KeeCommittee on Immunology, The University of Chicago, Chicago, IL 60637 Department of Pathology, The University of Chicago, Chicago, IL 60637 bkee@bsd.uchicago.edu.
University of Chicago · USLinköping University · SE

Funding

INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
Transcriptional Control of Natural Killer Cell DevelopmentR01AI106352 · NIAID · UNIVERSITY OF CHICAGO · PI KEE, BARBARA L. · 2014 to 2023
$4.6M
Transcriptional Regulation of Cardiac DevelopmentR01HL071063 · NHLBI · UNIVERSITY OF CHICAGO · PI SVENSSON, ERIC C · 2002 to 2010
$3.2M
ETS1 function in mature innate lymphoid cellsR21AI115388 · NIAID · UNIVERSITY OF CHICAGO · PI KEE, BARBARA L. · 2015 to 2016
$430k
Ets1Regulation of Natural Killer Cell Development and ActivationF32CA177235 · NCI · UNIVERSITY OF CHICAGO · PI ZOOK, ERIN CHRISTINE · 2013 to 2014
$99k
NCI NIH HHS F32 CA177235NHLBI NIH HHS R01 HL071063NIAID NIH HHS R01 AI106352NIAID NIH HHS R21 AI115388NIAID NIH HHS T32 AI007090
6 · The paper itself

Abstract

Group 2 innate lymphoid cells (ILC2s) are a subset of ILCs that play a protective role in the response to helminth infection, but they also contribute to allergic lung inflammation. Here, we report that the deletion of the ETS1 transcription factor in lymphoid cells resulted in a loss of ILC2s in the bone marrow and lymph nodes and that ETS1 promotes the fitness of the common progenitor of all ILCs. ETS1-deficient ILC2 progenitors failed to up-regulate messenger RNA for the E protein transcription factor inhibitor ID2, a critical factor for ILCs, and these cells were unable to expand in cytokine-driven in vitro cultures. In vivo, ETS1 was required for the IL-33-induced accumulation of lung ILC2s and for the production of the T helper type 2 cytokines IL-5 and IL-13. IL-25 also failed to elicit an expansion of inflammatory ILC2s when these cells lacked ETS1. Our data reveal ETS1 as a critical regulator of ILC2 expansion and cytokine production and implicate ETS1 in the regulation of Id2 at the inception of ILC2 development.

Indexed as

Immunity, InnateAnimalsCytokinesInhibitor of Differentiation Protein 2LymphocytesMiceMice, KnockoutProto-Oncogene Protein c-ets-1CytokinesEts1 protein, mouseIdb2 protein, mouseInhibitor of Differentiation Protein 2Proto-Oncogene Protein c-ets-1

Identifiers

PMID27069114
PMCPMC4854726
OpenAlexW2331724191

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.