Evidence map›Paper›PMID 32444635›Full record

ArticleNature communications2020

An integrated multi-omics approach identifies the landscape of interferon-α-mediated responses of human pancreatic beta cells.

Maikel L Colli, Mireia Ramos-Rodríguez, Ernesto S Nakayasu, Maria I Alvelos, Miguel Lopes, Jessica L E Hill, Jean-Valery Turatsinze, Alexandra Coomans de Brachène, Mark A Russell, Helena Raurell-Vila and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed, 1 pooled it
14.9field-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

99 citing papers in PubMed, 1 synthesis or guideline pooled it, 133 citations in OpenAlex.

  1. Pooled it
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  10. A surviving beta cell subpopulation enriched in patients with T1D.bioRxiv : the preprint server for biology · 2026
    Article
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  12. From bats to humans: uncoveringbioRxiv : the preprint server for biology · 2026
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39 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

22 authors at 6 institutions in 6 countries.

Maikel L ColliULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium. mcolli@ulb.ac.be.ORCID http://orcid.org/0000-0002-2200-4761
Mireia Ramos-RodríguezEndocrine Regulatory Genomics, Department of Experimental & Health Sciences, University Pompeu Fabra, 08003, Barcelona, Spain.
Ernesto S NakayasuBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.ORCID http://orcid.org/0000-0002-4056-2695
Maria I AlvelosULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium.
Miguel LopesULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium.
Jessica L E HillInstitute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, EX2 5DW, UK.
Jean-Valery TuratsinzeULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium.ORCID http://orcid.org/0000-0001-9492-6274
Alexandra Coomans de BrachèneULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium.
Mark A RussellInstitute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, EX2 5DW, UK.
Helena Raurell-VilaEndocrine Regulatory Genomics, Department of Experimental & Health Sciences, University Pompeu Fabra, 08003, Barcelona, Spain.
Angela CastelaULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium.
Jonàs Juan-MateuULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium.
Bobbie-Jo M Webb-RobertsonBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Lars KrogvoldDivision of Pediatric and Adolescent Medicine, Faculty of Medicine, Oslo University Hospital, Oslo, Norway.
Knut Dahl-JorgensenDivision of Pediatric and Adolescent Medicine, Faculty of Medicine, Oslo University Hospital, Oslo, Norway.
Lorella MarselliDepartment of Clinical and Experimental Medicine, Islet Cell Laboratory, University of Pisa, 56126, Pisa, Italy.ORCID http://orcid.org/0000-0002-6698-2962
Piero MarchettiDepartment of Clinical and Experimental Medicine, Islet Cell Laboratory, University of Pisa, 56126, Pisa, Italy.
Sarah J RichardsonInstitute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, EX2 5DW, UK.ORCID http://orcid.org/0000-0002-1160-6062
Noel G MorganInstitute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, EX2 5DW, UK.ORCID http://orcid.org/0000-0003-1537-8113
Thomas O MetzBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.ORCID http://orcid.org/0000-0001-6049-3968
Lorenzo PasqualiEndocrine Regulatory Genomics, Department of Experimental & Health Sciences, University Pompeu Fabra, 08003, Barcelona, Spain.ORCID http://orcid.org/0000-0003-2423-1826
Décio L EizirikULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, Brussels, 1070, Belgium.ORCID http://orcid.org/0000-0003-2453-5889
Université Libre de Bruxelles · BEUniversity of Exeter · GBPacific Northwest National Laboratory · USUniversitat Pompeu Fabra · ESOslo University Hospital · NOUniversity of Pisa · IT

Funding

Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
Biomarkers Of Beta Cell Stress In Type 1 Diabetes (BetaMarker)UC4DK104166 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI EIZIRIK, DECIO LAKS, EVANS-MOLINA, CARMELLA · 2014 to 2014
$2.4M
Medical Research Council MR/P010695/1NIDDK NIH HHS P30 DK097512NIDDK NIH HHS UC4 DK104166
6 · The paper itself

Abstract

Interferon-α (IFNα), a type I interferon, is expressed in the islets of type 1 diabetic individuals, and its expression and signaling are regulated by T1D genetic risk variants and viral infections associated with T1D. We presently characterize human beta cell responses to IFNα by combining ATAC-seq, RNA-seq and proteomics assays. The initial response to IFNα is characterized by chromatin remodeling, followed by changes in transcriptional and translational regulation. IFNα induces changes in alternative splicing (AS) and first exon usage, increasing the diversity of transcripts expressed by the beta cells. This, combined with changes observed on protein modification/degradation, ER stress and MHC class I, may expand antigens presented by beta cells to the immune system. Beta cells also up-regulate the checkpoint proteins PDL1 and HLA-E that may exert a protective role against the autoimmune assault. Data mining of the present multi-omics analysis identifies two compound classes that antagonize IFNα effects on human beta cells.

Indexed as

Alternative SplicingCells, CulturedChromatinData MiningDiabetes Mellitus, Type 1Gene Expression RegulationGene Regulatory NetworksHumansInsulin-Secreting CellsInterferon-alphaProtein Interaction MapsProteomicsTranscription FactorsTranscription Initiation SiteChromatinInterferon-alphaTranscription Factors

Identifiers

PMID32444635
PMCPMC7244579
OpenAlexW3028068117

What Socratic 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 Socratic graph.