Evidence map›Paper›PMID 30574141›Full record

ArticleFrontiers in immunology2018

MicroRNA-31 Reduces the Motility of Proinflammatory T Helper 1 Lymphocytes.

Markus Bardua, Claudia Haftmann, Pawel Durek, Kerstin Westendorf, Antje Buttgereit, Cam Loan Tran, Mairi McGrath, Melanie Weber, Katrin Lehmann, Richard Kwasi Addo and 8 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  7. Non-Coding RNAs in CD4Frontiers in immunology · 2020
    Review
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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

18 authors at 3 institutions in 1 country.

Markus BarduaDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Claudia HaftmannDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Pawel DurekDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Kerstin WestendorfDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Antje ButtgereitDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Cam Loan TranDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Mairi McGrathDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Melanie WeberDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Katrin LehmannDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Richard Kwasi AddoDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Gitta Anne HeinzDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Anna-Barbara StittrichInstitute for Medical Immunology, Charité-Universitätsmedizin, Berlin, Germany.
Patrick MaschmeyerDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Helena RadbruchDepartment of Neuropathology, Charité-Universitätsmedizin, Berlin, Germany.
Michael LohoffInstitute for Medical Microbiology and Hospital Hygiene, University of Marburg, Marburg, Germany.
Hyun-Dong ChangDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Andreas RadbruchDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Mir-Farzin MashreghiDeutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
German Rheumatism Research Centre · DECharité - Universitätsmedizin Berlin · DEPhilipps University of Marburg · DE

Funding

European Research Council 268987
6 · The paper itself

Abstract

Proinflammatory type 1 T helper (Th1) cells are enriched in inflamed tissues and contribute to the maintenance of chronic inflammation in rheumatic diseases. Here we show that the microRNA- (miR-) 31 is upregulated in murine Th1 cells with a history of repeated reactivation and in memory Th cells isolated from the synovial fluid of patients with rheumatic joint disease. Knock-down of miR-31 resulted in the upregulation of genes associated with cytoskeletal rearrangement and motility and induced the expression of target genes involved in T cell activation, chemokine receptor- and integrin-signaling. Accordingly, inhibition of miR-31 resulted in increased migratory activity of repeatedly activated Th1 cells. The transcription factors T-bet and FOXO1 act as positive and negative regulators of T cell receptor (TCR)-mediated miR-31 expression, respectively. Taken together, our data show that a gene regulatory network involving miR-31, T-bet, and FOXO1 controls the migratory behavior of proinflammatory Th1 cells.

Indexed as

AnimalsCell MovementFemaleForkhead Box Protein O1HumansInflammationMaleMiceMice, Inbred BALB CMice, KnockoutMicroRNAsT-bet Transcription FactorT-Box Domain ProteinsTh1 CellsForkhead Box Protein O1FOXO1 protein, humanFoxo1 protein, mouseMicroRNAsMIRN31 microRNA, humanMirn31 microRNA, mouseT-bet Transcription FactorT-Box Domain ProteinsantagomirsCD4miR-31miRNAregulatory networkstarget identificationT cell migrationTh1 cells

Identifiers

PMID30574141
PMCPMC6291424
OpenAlexW2905036189

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.