Evidence map›Paper›PMID 27974684›Full record

ArticleOncotarget2017

Macrophage production and activation are dependent on TRIM33.

Anne-Sophie Gallouet, Federica Ferri, Vanessa Petit, Aude Parcelier, Daniel Lewandowski, Nathalie Gault, Vilma Barroca, Stéphanie Le Gras, Eric Soler, Frank Grosveld and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. The Roles of TIF1γ in Cancer.Frontiers in oncology · 2019
    Review
  14. Review
  15. Review
  16. Intracellular Antiviral Immunity.Advances in virus research · 2018
    Review
  17. Article
  18. Review
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

12 authors at 10 institutions in 2 countries.

Anne-Sophie GallouetCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Federica FerriCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Vanessa PetitCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Aude ParcelierCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Daniel LewandowskiCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Nathalie GaultCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Vilma BarrocaCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Stéphanie Le GrasDepartment of Functional Genomics and Cancer, Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, BP 163, 67404 Illkirch Cedex, C. U. Strasbourg, France.
Eric SolerCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Frank GrosveldDepartment of Cell Biology, Erasmus Medical Center, DR Molenwaterplein 50, 3015GE, Rotterdam, The Netherlands.
Irwin DavidsonDepartment of Functional Genomics and Cancer, Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, BP 163, 67404 Illkirch Cedex, C. U. Strasbourg, France.
Paul-Henri RomeoCEA/DRF/iRCM/LRTS, 92265 Fontenay-aux-Roses cedex, France.
Université Paris-Sud · FRCEA Paris-Saclay - Etablissement de Fontenay-aux-roses · FRCentre National de la Recherche Scientifique · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRDélégation Paris 7 · FRErasmus MC · NLInserm · FRInstitut de génétique et de biologie moléculaire et cellulaire · FRLa Ligue Contre le Cancer · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tripartite motif (TRIM) family of proteins plays important roles in innate immunity and antimicrobial infection. None of these proteins has been shown to directly regulate transcription of genes in monocyte/macrophage except TRIM33 that we have recently shown to be a macrophage specific transcriptional inhibitor of Ifnb1. Using ChIP-seq analyses, we now report that TRIM33 is bound to two fold more genes in immature than in mature myeloid cell lines. When located near the same genes, TRIM33 is bound to different sequences in the two cell lines suggesting a role of TRIM33 in both immature and mature myeloid cells. Accordingly, expression of TRIM33 in immature myeloid cells is necessary for efficient production of small peritoneal macrophages, monocytes and bone marrow derived macrophage (BMDM) and TRIM33 targets a subset of genes involved in the inflammatory response only in mature myeloid cells. Functionally, this targeting is associated with impaired repression of pathways regulating the late phases of lipopolysaccharide (LPS) activation of BMDM and a high sensitivity to LPS in vivo when the trim33 gene is inactivated in mature myeloid cells. These findings pinpoint TRIM33 as an important transcriptional actor of monocyte/macrophage mediated inflammation.

Indexed as

Macrophage ActivationAnimalsCells, CulturedChromatinChromatin ImmunoprecipitationDNAGene Regulatory NetworksLipopolysaccharidesMacrophagesMiceMyeloid CellsRAW 264.7 CellsSequence Analysis, DNATranscription FactorsChromatinDNALipopolysaccharidesTranscription FactorsTrim33 protein, mouseinflammationmacrophagemyeloid differentiationPU.1TRIM33

Identifiers

PMID27974684
PMCPMC5354896
OpenAlexW2560440159

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.