Evidence map›Paper›PMID 26834155›Full record

ArticleThe Journal of experimental medicine2016

miR-23∼27∼24 clusters control effector T cell differentiation and function.

Sunglim Cho, Cheng-Jang Wu, Tomoharu Yasuda, Leilani O Cruz, Aly Azeem Khan, Ling-Li Lin, Duc T Nguyen, Marina Miller, Hyang-Mi Lee, Ming-Ling Kuo and 4 more

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 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% 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

82 citing papers in PubMed, 1 synthesis or guideline pooled it, 135 citations in OpenAlex.

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22 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

14 authors at 5 institutions in 3 countries.

Sunglim ChoDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Cheng-Jang WuDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093 Department of Microbiology and Immunology, College of Medicine, Chang Gung University, 333 Taoyuan, Taiwan.
Tomoharu YasudaImmune Regulation and Cancer, Max-Delbrück-Center for Molecular Medicine, 13125 Berlin, Germany.
Leilani O CruzDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Aly Azeem KhanToyota Technological Institute at Chicago, Chicago, IL 60637.
Ling-Li LinDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Duc T NguyenDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Marina MillerDepartment of Medicine, University of California, San Diego, La Jolla, CA 92093.
Hyang-Mi LeeDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Ming-Ling KuoDepartment of Microbiology and Immunology, College of Medicine, Chang Gung University, 333 Taoyuan, Taiwan.
David H BroideDepartment of Medicine, University of California, San Diego, La Jolla, CA 92093.
Klaus RajewskyImmune Regulation and Cancer, Max-Delbrück-Center for Molecular Medicine, 13125 Berlin, Germany.
Alexander Y RudenskyHoward Hughes Medical Institute and Immunology Program, Ludwig Center at Memorial Sloan-Kettering Cancer Center, Memorial Sloan-Kettering Cancer Center, New York, NY 10065.
Li-Fan LuDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093 Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093 lifanlu@ucsd.edu.
University of California, San Diego · USMax Delbrück Center · DEChang Gung University · TWHoward Hughes Medical Institute · USToyota Technological Institute at Chicago · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Role of microRNAs in regulatory T cell-mediated immunological tolerance and T celR01AI108651 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2014 to 2024
$4.0M
Function of microRNAs in controlling regulatory T cell biologyR00AI089935 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2012 to 2013
$493k
The role of SOCS1 repression by miR-155 in regulating immune responsivenessR21AI103646 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2013 to 2014
$426k
Function of microRNAs in controlling regulatory T cell biologyK99AI089935 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI LU, LI-FAN · 2011 to 2011
$94k
NCI NIH HHS P30 CA008748NIAID NIH HHS AI089935NIAID NIH HHS AI103646NIAID NIH HHS AI108651NIAID NIH HHS K99 AI089935NIAID NIH HHS R00 AI089935NIAID NIH HHS R01 AI108651NIAID NIH HHS R21 AI103646
6 · The paper itself

Abstract

Coordinated repression of gene expression by evolutionarily conserved microRNA (miRNA) clusters and paralogs ensures that miRNAs efficiently exert their biological impact. Combining both loss- and gain-of-function genetic approaches, we show that the miR-23∼27∼24 clusters regulate multiple aspects of T cell biology, particularly helper T (Th) 2 immunity. Low expression of this miRNA family confers proper effector T cell function at both physiological and pathological settings. Further studies in T cells with exaggerated regulation by individual members of the miR-23∼27∼24 clusters revealed that miR-24 and miR-27 collaboratively limit Th2 responses through targeting IL-4 and GATA3 in both direct and indirect manners. Intriguingly, although overexpression of the entire miR-23 cluster also negatively impacts other Th lineages, enforced expression of miR-24, in contrast to miR-23 and miR-27, actually promotes the differentiation of Th1, Th17, and induced regulatory T cells, implying that under certain conditions, miRNA families can fine tune the biological effects of their regulation by having individual members antagonize rather than cooperate with each other. Together, our results identify a miRNA family with important immunological roles and suggest that tight regulation of miR-23∼27∼24 clusters in T cells is required to maintain optimal effector function and to prevent aberrant immune responses.

Indexed as

AnimalsAsthmaCell DifferentiationDisease Models, AnimalGATA3 Transcription FactorGene Expression RegulationGene Regulatory NetworksInterleukin-4Lymphocyte ActivationMiceMice, TransgenicMicroRNAsMultigene FamilyPhenotypeTh2 CellsT-Lymphocytes, Helper-InducerGata3 protein, mouseGATA3 Transcription FactorInterleukin-4MicroRNAsMirn23b microRNA, mouseMirn24 microRNA, mouseMirn27 microRNA, mouse

Identifiers

PMID26834155
PMCPMC4749926
OpenAlexW2268476648

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.