Evidence map›Paper›PMID 29282318›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

SRC1 promotes Th17 differentiation by overriding Foxp3 suppression to stimulate RORγt activity in a PKC-θ-dependent manner.

Subha Sen, Fei Wang, Jing Zhang, Zhiheng He, Jian Ma, Yousang Gwack, Jianming Xu, Zuoming Sun

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

27 citing papers in PubMed, 38 citations in OpenAlex.

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  12. SRC2 controls CD4Proceedings of the National Academy of Sciences of the United States of America · 2023
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  17. Th17 cell master transcription factor RORC2 regulates HIV-1 gene expression and viral outgrowth.Proceedings of the National Academy of Sciences of the United States of America · 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

8 authors at 3 institutions in 1 country.

Subha SenDivision of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010.
Fei WangDivision of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010.
Jing ZhangDivision of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010.
Zhiheng HeDivision of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010.
Jian MaDivision of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010.
Yousang GwackDepartment of Physiology, David Geffen School of Medicine, University of California, Los Angeles, CA 90095.
Jianming XuDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030.
Zuoming SunDivision of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010; zsun@coh.org.ORCID 0000-0003-1896-6666
City of Hope · USBaylor College of Medicine · USUniversity of California, Los Angeles · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Steroid nuclear receptor coactivators in T cell differentiationR01AI109644 · NIAID · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI Zuoming Sun · 2014 to 2026
$6.9M
Novel regulators of store-operated Ca2+ entry in immune systemsR01AI083432 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GWACK, YOUSANG · 2009 to 2020
$3.8M
PKC-theta function in RORgammat-regulated Th17 differentiationR01AI053147 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUN, ZUOMING · 2004 to 2015
$3.7M
NCI NIH HHS P30 CA016042NCI NIH HHS P30 CA033572NIAID NIH HHS R01 AI053147NIAID NIH HHS R01 AI083432NIAID NIH HHS R01 AI109644
6 · The paper itself

Abstract

Th17 cells are major players in multiple autoimmune diseases and are developmentally contingent on reciprocal functionality between the transcription factor Retineic acid receptor-related orphan nuclear receptor gamma (RORγt) and Forkhead box protein P3 (Foxp3). Here we deciphered a previously unappreciated role of Steroid receptor coactivator 1 (SRC1) in defining the lineage decision for the development of Th17 versus induced T-regulatory (iTreg) cells. We demonstrate that SRC1 functions as a critical coactivator for RORγt in vivo to promote the functional dominance of RORγt over Foxp3 and thus establishing an unopposed Th17 differentiation program. In the absence of SRC1, T cell polarization resulted in decreased IL-17

Indexed as

Amino Acid SequenceAnimalsCell DifferentiationForkhead Transcription FactorsGene DeletionGene Expression Regulation, EnzymologicInterleukinsMiceNuclear Receptor Coactivator 1Nuclear Receptor Subfamily 1, Group F, Member 3Protein Kinase C-thetaTh17 CellsForkhead Transcription FactorsFoxp3 protein, mouseInterleukinsNcoa1 protein, mouseNuclear Receptor Coactivator 1Nuclear Receptor Subfamily 1, Group F, Member 3Protein Kinase C-thetaRorc protein, mouseEAET cell differentiationTh17Treg

Identifiers

PMID29282318
PMCPMC5776998
OpenAlexW2776612223

What OpenQuestion holds

Textmetadata
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.