Evidence map›Paper›PMID 30664289›Full record

ArticleStem cells (Dayton, Ohio)2019

Global Proteomic and Methylome Analysis in Human Induced Pluripotent Stem Cells Reveals Overexpression of a Human TLR3 Affecting Proper Innate Immune Response Signaling.

Jordi Requena, Ana Belen Alvarez-Palomo, Montserrat Codina-Pascual, Raul Delgado-Morales, Sebastian Moran, Manel Esteller, Martí Sal, Manel Juan, Anna Boronat Barado, Antonella Consiglio and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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 10 institutions in 5 countries.

Jordi RequenaMolecular Genetics and Control of Pluripotency Laboratory, Faculty of Medicine, Department of Biomedicine, University of Barcelona, Barcelona, Spain.
Ana Belen Alvarez-PalomoMolecular Genetics and Control of Pluripotency Laboratory, Faculty of Medicine, Department of Biomedicine, University of Barcelona, Barcelona, Spain.
Montserrat Codina-PascualGenetics Unit, Department of Biomedicine, Faculty of Medicine, University of Barcelona, IDIBAPS and Hospital Clinic, Barcelona, Spain.
Raul Delgado-MoralesCancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Catalonia, Spain.
Sebastian MoranCancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Catalonia, Spain.
Manel EstellerCancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Catalonia, Spain.
Martí SalMolecular Genetics and Control of Pluripotency Laboratory, Faculty of Medicine, Department of Biomedicine, University of Barcelona, Barcelona, Spain.
Manel JuanService of Immunology, Hospital Clinic, Hospital Sant Joan de Déu, Barcelona, Spain.
Anna Boronat BaradoService of Immunology, Hospital Clinic, Hospital Sant Joan de Déu, Barcelona, Spain.
Antonella ConsiglioDepartment of Pathology and Experimental Therapeutics, Bellvitge University Hospital-IDIBELL, Hospitalet de Llobregat 08908, Spain.
Orleigh Addeleccia BogleGenetics Unit, Department of Biomedicine, Faculty of Medicine, University of Barcelona, IDIBAPS and Hospital Clinic, Barcelona, Spain.
Ernst WolvetangStem Cell Engineering Group, Australian Institute for Bioengineering and Nanotechnology, University of Queensland, Queensland, Brisbane, Australia.
Dmitry OvchinnikovStem Cell Engineering Group, Australian Institute for Bioengineering and Nanotechnology, University of Queensland, Queensland, Brisbane, Australia.
Inaki AlvarezImmunology Unit, Department of Cell Biology, Physiology and Immunology and Institute of Biotechnology and Biomedicine, Autonomous University of Barcelona, Bellaterra, Spain.
Dolores JaraquemadaImmunology Unit, Department of Cell Biology, Physiology and Immunology and Institute of Biotechnology and Biomedicine, Autonomous University of Barcelona, Bellaterra, Spain.
Jovita Mezquita-PlaMolecular Genetics and Control of Pluripotency Laboratory, Faculty of Medicine, Department of Biomedicine, University of Barcelona, Barcelona, Spain.
Rafael OlivaGenetics Unit, Department of Biomedicine, Faculty of Medicine, University of Barcelona, IDIBAPS and Hospital Clinic, Barcelona, Spain.ORCID 0000-0003-4876-2410
Michael J EdelMolecular Genetics and Control of Pluripotency Laboratory, Faculty of Medicine, Department of Biomedicine, University of Barcelona, Barcelona, Spain.ORCID 0000-0002-5619-8680
Hospital Clínic de Barcelona · ESUniversitat de Barcelona · ESBellvitge University Hospital · ESHospital Sant Joan de Déu Barcelona · ESThe University of Queensland · AUUniversitat Autònoma de Barcelona · ESInstitució Catalana de Recerca i Estudis Avançats · ESInstitut Barcelona d'Estudis Internacionals · ESInstitute for Research in Biomedicine · ESUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

When considering the clinical applications of autologous cell replacement therapy of human induced pluripotent stem cells (iPSC)-derived cells, there is a clear need to better understand what the immune response will be before we embark on extensive clinical trials to treat or model human disease. We performed a detailed assessment comparing human fibroblast cell lines (termed F1) reprogrammed into human iPSC and subsequently differentiated back to fibroblast cells (termed F2) or other human iPSC-derived cells including neural stem cells (NSC) made from either retroviral, episomal, or synthetic mRNA cell reprogramming methods. Global proteomic analysis reveals the main differences in signal transduction and immune cell protein expression between F1 and F2 cells, implicating wild type (WT) toll like receptor protein 3 (TLR3). Furthermore, global methylome analysis identified an isoform of the human TLR3 gene that is not epigenetically reset correctly upon differentiation to F2 cells resulting in a hypomethylated transcription start site in the TLR3 isoform promoter and overexpression in most human iPSC-derived cells not seen in normal human tissue. The human TLR3 isoform in human iPSC-NSC functions to suppress NF-KB p65 signaling pathway in response to virus (Poly IC), suggesting suppressed immunity of iPSC-derived cells to viral infection. The sustained WT TLR3 and TLR3 isoform overexpression is central to understanding the altered immunogenicity of human iPSC-derived cells calling for screening of human iPSC-derived cells for TLR3 expression levels before applications. Stem Cells 2019;37:476-488.

Indexed as

EpigenomeHumansImmunity, InnateInduced Pluripotent Stem CellsProteomicsSignal TransductionToll-Like Receptor 3TLR3 protein, humanToll-Like Receptor 3CytokineHuman leukocyte antigenImmune responseInduced pluripotent stem cellsInflammationMHC-INeural stem cellsToll like receptor

Identifiers

PMID30664289
PMCPMC6487958
OpenAlexW2907269451

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.