Evidence map›Paper›PMID 28904128›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Integration of Kinase and Calcium Signaling at the Level of Chromatin Underlies Inducible Gene Activation in T Cells.

Ruth Brignall, Pierre Cauchy, Sarah L Bevington, Bethany Gorman, Angela O Pisco, James Bagnall, Christopher Boddington, William Rowe, Hazel England, Kevin Rich and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

41 citing papers in PubMed, 72 citations in OpenAlex.

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  11. Antigen perception in T cells by long-term Erk and NFAT signaling dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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  14. How CD4Biomedicines · 2023
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  15. Regulatory role of NFAT1 signaling in articular chondrocyte activities and osteoarthritis pathogenesis.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2023
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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

17 authors at 5 institutions in 2 countries.

Ruth BrignallFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Pierre CauchyInstitute of Biomedical Research, College of Medicine and Dentistry, University of Birmingham, Birmingham B15 2TT, United Kingdom.ORCID 0000-0002-0659-0799
Sarah L BevingtonInstitute of Biomedical Research, College of Medicine and Dentistry, University of Birmingham, Birmingham B15 2TT, United Kingdom.
Bethany GormanInstitute of Biomedical Research, College of Medicine and Dentistry, University of Birmingham, Birmingham B15 2TT, United Kingdom.
Angela O PiscoCentre for Stem Cells and Regenerative Medicine, King's College London, London SE1 9RT, United Kingdom.ORCID 0000-0003-0142-2355
James BagnallFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.ORCID 0000-0003-1735-5855
Christopher BoddingtonFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
William RoweDepartment of Chemistry, Loughborough University, Loughborough LE11 3TU, United Kingdom.
Hazel EnglandFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.ORCID 0000-0002-8324-614X
Kevin RichFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.ORCID 0000-0001-7322-496X
Lorraine SchmidtFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Nigel P DyerWarwick Systems Biology Centre, University of Warwick, Coventry CV4 7AL, United Kingdom.ORCID 0000-0001-6158-0510
Mark A TravisFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Sascha OttWarwick Systems Biology Centre, University of Warwick, Coventry CV4 7AL, United Kingdom.
Dean A JacksonFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Peter N CockerillInstitute of Biomedical Research, College of Medicine and Dentistry, University of Birmingham, Birmingham B15 2TT, United Kingdom; pawel.paszek@manchester.ac.uk p.n.cockerill@bham.ac.uk.
Pawel PaszekFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom; pawel.paszek@manchester.ac.uk p.n.cockerill@bham.ac.uk.ORCID 0000-0002-0363-0716
Manchester Academic Health Science Centre · GBUniversity of Birmingham · GBUniversity of Warwick · GBKing's College - North Carolina · USLoughborough University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I017976/1Biotechnology and Biological Sciences Research Council BB/K003097/1Medical Research Council MR/K015885/1Medical Research Council MR/M00242X/1Medical Research Council MR/P001319/1Wellcome Trust 203128
6 · The paper itself

Abstract

TCR signaling pathways cooperate to activate the inducible transcription factors NF-κB, NFAT, and AP-1. In this study, using the calcium ionophore ionomycin and/or PMA on Jurkat T cells, we show that the gene expression program associated with activation of TCR signaling is closely related to specific chromatin landscapes. We find that calcium and kinase signaling cooperate to induce chromatin remodeling at ∼2100 chromatin regions, which demonstrate enriched binding motifs for inducible factors and correlate with target gene expression. We found that these regions typically function as inducible enhancers. Many of these elements contain composite NFAT/AP-1 sites, which typically support cooperative binding, thus further reinforcing the need for cooperation between calcium and kinase signaling in the activation of genes in T cells. In contrast, treatment with PMA or ionomycin alone induces chromatin remodeling at far fewer regions (∼600 and ∼350, respectively), which mostly represent a subset of those induced by costimulation. This suggests that the integration of TCR signaling largely occurs at the level of chromatin, which we propose plays a crucial role in regulating T cell activation.

Indexed as

Chromatin Assembly and DisassemblyCalciumCalcium IonophoresChromatinHumansJurkat CellsLymphocyte ActivationNFATC Transcription FactorsNF-kappa BPhosphotransferasesReceptor Cross-TalkReceptors, Antigen, T-CellSignal TransductionT-LymphocytesTranscription Factor AP-1CalciumCalcium IonophoresChromatinNFATC Transcription FactorsNF-kappa BPhosphotransferasesReceptors, Antigen, T-CellTranscription Factor AP-1

Identifiers

PMID28904128
PMCPMC5632840
OpenAlexW2749779298

What OpenQuestion holds

Textmetadata
LicenceTDM
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.