Evidence map›Paper›PMID 27156386›Full record

ArticleImmunity2016

Transforming Growth Factor-β Signaling Guides the Differentiation of Innate Lymphoid Cells in Salivary Glands.

Victor S Cortez, Luisa Cervantes-Barragan, Michelle L Robinette, Jennifer K Bando, Yaming Wang, Theresa L Geiger, Susan Gilfillan, Anja Fuchs, Eric Vivier, Joe C Sun and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 165 papers.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed
16.2field-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

165 citing papers in PubMed, 241 citations in OpenAlex.

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105 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

12 authors at 3 institutions in 2 countries.

Victor S CortezDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA.
Luisa Cervantes-BarraganDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA.
Michelle L RobinetteDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA.
Jennifer K BandoDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA.
Yaming WangDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA.
Theresa L GeigerImmunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Susan GilfillanDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA.
Anja FuchsDepartment of Surgery, Section of Acute and Critical Care Surgery, Washington University School of Medicine, St Louis, MO 63108, USA.
Eric VivierCentre d'Immunologie de Marseille-Luminy, UM2 Aix-Marseille Université, Marseille, France.
Joe C SunImmunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Marina CellaDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA.
Marco ColonnaDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63108, USA. Electronic address: mcolonna@pathology.wustl.edu.
Washington University in St. Louis · USMemorial Sloan Kettering Cancer Center · USCentre d’Immunologie de Marseille-Luminy · FR

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
ImmGen: Gene Expression and Regulation in Immune CellsR24AI072073 · NIAID · JOSLIN DIABETES CENTER · PI CHRISTOPHE O. BENOIST · 2007 to 2026
$28.5M
Mucosal Immune Defense Mechanisms of the Urinary BladderU01AI095542 · NIAID · WASHINGTON UNIVERSITY · PI COLONNA, MARCO, HULTGREN, SCOTT J. · 2011 to 2020
$9.8M
The role of TGFbeta in development and function of salivary gland innate lymphoid cellsR01DE025884 · NIDCR · WASHINGTON UNIVERSITY · PI COLONNA, MARCO, WEISMAN, GARY ANDREW · 2017 to 2021
$3.5M
THE ROLE OF NK-22 CELLS IN ANTI-HIV-1 MUCOSAL IMMUNITYR01DE021255 · NIDCR · WASHINGTON UNIVERSITY · PI COLONNA, MARCO · 2010 to 2014
$1.9M
IL-22 IN OBESITY AND OBESITY-ASSOCIATED CANCERR01CA176695 · NCI · WASHINGTON UNIVERSITY · PI CELLA, MARINA · 2013 to 2017
$1.6M
CRTAM-CADM1 INTERACTION IN THE BIOLOGY OF GUT LYMPHOCYTESR01DK103039 · NIDDK · WASHINGTON UNIVERSITY · PI COLONNA, MARCO · 2015 to 2018
$1.4M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA176695NIAID NIH HHS R24 AI072073NIAID NIH HHS U01 AI095542NIDCR NIH HHS R01 DE021255NIDCR NIH HHS R01 DE025884NIDDK NIH HHS R01 DK103039
6 · The paper itself

Abstract

The signals guiding differentiation of innate lymphoid cells (ILCs) within tissues are not well understood. Salivary gland (SG) ILCs as well as liver and intestinal intraepithelial ILC1 have markers that denote tissue residency and transforming growth factor-β (TGF-β) imprinting. We deleted Tgfbr2 in cells expressing the ILC and NK marker NKp46 and found that SG ILCs were reduced in number. They lost distinct tissue markers, such as CD49a, and the effector molecules TRAIL and CD73. Expression of the transcription factor Eomes, which promotes NK cell differentiation, was elevated. Conversely, Eomes deletion in NKp46(+) cells enhanced TGF-β-imprinting of SG ILCs. Thus, TGF-β induces SG ILC differentiation by suppressing Eomes. TGF-β acted through a JNK-dependent, Smad4-independent pathway. Transcriptome analysis demonstrated that SG ILCs had characteristic of both NK cells and ILC1. Finally, TGF-β imprinting of SG ILCs was synchronized with SG development, highlighting the impact of tissue microenvironment on ILC development.

Indexed as

Cell DifferentiationAnimalsAntigens, LyCellular MicroenvironmentGene Expression ProfilingImmunity, InnateKiller Cells, NaturalLymphocytesMAP Kinase Kinase 4MiceMice, KnockoutNatural Cytotoxicity Triggering Receptor 1Protein Serine-Threonine KinasesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type IISalivary GlandsAntigens, LyEomes protein, mouseMAP Kinase Kinase 4Natural Cytotoxicity Triggering Receptor 1Ncr1 protein, mouseProtein Serine-Threonine KinasesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type IISmad4 ProteinSmad4 protein, mouseT-Box Domain ProteinsTransforming Growth Factor betadevelopmentinnate lymphoid cellssalivary glandsignalingTGF-βtranscription factors

Identifiers

PMID27156386
PMCPMC5114145
OpenAlexW2345466072

What OpenQuestion holds

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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.