Evidence map›Paper›PMID 28588282›Full record

ArticleScientific reports2017

Comparison and immunobiological characterization of retinoic acid inducible gene-I-like receptor expression in mesenchymal stromal cells.

Gordana Raicevic, Mehdi Najar, Hélène Busser, Emerence Crompot, Dominique Bron, Michel Toungouz, Laurence Lagneaux

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Drug-resistant seizures associated with hyperinflammatory monocytes in FIRES.Annals of clinical and translational neurology · 2023
    Article
  7. Review
  8. Article
  9. Immune Reconstitution Disorders: Spotlight on Interferons.International journal of biomedical investigation · 2019
    Article
  10. Article
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

7 authors at 3 institutions in 1 country.

Gordana RaicevicLaboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium. gordana.raicevic@ulb.ac.be.
Mehdi NajarLaboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Hélène BusserLaboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Emerence CrompotLaboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Dominique BronLaboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Michel ToungouzLaboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Laurence LagneauxLaboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Institut Jules Bordet · BEErasmus Hospital · BEUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to their immunomodulatory and regenerative properties, Mesenchymal stromal cells (MSC) have generated major interests in several clinical settings including transplantation and inflammatory diseases. MSC functions can be influenced by their tissue origin. Their microenvironment strongly affects their biology notably through TLR sensing. In this study, we show that MSC isolated from four different sources express another type of cytosolic pathogen recognition receptors known as retinoic acid inducible gene-I (RIG-I)-like receptors (RLR). RLR activation in MSC induces the production of Type I IFN (IFN-β) and Type III IFN (IFN-λ1). The highest producers are adipose tissue(AT)-MSC. We further show that Interferon production is induced through TBK1/IKK-ε signaling and IRF7 phosphorylation. Depending on MSC source, the knockdown of TLR3 and/or RIG-I decreases the MSC response to RLR ligand poly(I:C)/Lyovec. Among the different MSC types, AT-MSCs display the highest sensitivity to viral stimuli as shown by the alteration of their viability after prolonged stimulation. Our work indicates that this could be linked to an increase of pro-apoptotic Noxa expression. Finally, the expression of IDO1 and LIF upon RLR activation indicate the increase of MSC immunomodulatory potential, especially in AT-MSCs. Altogether, these data should be considered when designing MSC-based therapy in clinical settings where inflammation or infection are present.

Indexed as

Gene Expression RegulationCell SurvivalCytokinesDEAD Box Protein 58HumansI-kappa B KinaseImmunophenotypingInterferon-Induced Helicase, IFIH1Interferon Regulatory Factor-7Leukemia Inhibitory FactorMesenchymal Stem CellsOrgan SpecificityPoly I-CReceptors, ImmunologicReceptors, Retinoic AcidRNA, MessengerCytokinesDEAD Box Protein 58IFIH1 protein, humanI-kappa B KinaseIKBKE protein, humanInterferon-Induced Helicase, IFIH1Interferon Regulatory Factor-7IRF7 protein, humanLeukemia Inhibitory FactorLIF protein, humanPLAAT4 protein, humanPoly I-CReceptors, ImmunologicReceptors, Retinoic AcidRIGI protein, humanRNA, MessengerTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanToll-Like Receptor 3

Identifiers

PMID28588282
PMCPMC5460162
OpenAlexW2619523252

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.