Evidence map›Paper›PMID 27702798›Full record

ArticleBlood2016

miR-125b controls monocyte adaptation to inflammation through mitochondrial metabolism and dynamics.

Isabelle Duroux-Richard, Christine Roubert, Meryem Ammari, Jessy Présumey, Joachim R Grün, Thomas Häupl, Andreas Grützkau, Charles-Henri Lecellier, Valérie Boitez, Patrice Codogno and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

56 citing papers in PubMed, 85 citations in OpenAlex.

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  16. Guidelines for mitochondrial RNA analysis.Molecular therapy. Nucleic acids · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Role of UPRFrontiers in cellular and infection microbiology · 2023
    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

14 authors at 6 institutions in 2 countries.

Isabelle Duroux-RichardINSERM, U1183, CHU Saint Eloi, Montpellier, France.
Christine RoubertExploratory Unit, Sanofi R&D, Montpellier, France.
Meryem AmmariINSERM, U1183, CHU Saint Eloi, Montpellier, France.
Jessy PrésumeyINSERM, U1183, CHU Saint Eloi, Montpellier, France.
Joachim R GrünDeutsches Rheuma-Forschungszentrum Berlin, an Institute of the Leibniz Association, Berlin, Germany.
Thomas HäuplRheumatologie Department, Charité Universitätsmedizin Berlin, Berlin, Germany.
Andreas GrützkauDeutsches Rheuma-Forschungszentrum Berlin, an Institute of the Leibniz Association, Berlin, Germany.
Charles-Henri LecellierInstitut de génétique moléculaire de Montpellier, CNRS Unité mixte de recherche 5535, Unité mixte de service France, Montpellier, France.
Valérie BoitezInstitut Necker-Enfants Malades, INSERM, U1151, CNRS Unité mixte de recherche 8253, Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
Patrice CodognoInstitut Necker-Enfants Malades, INSERM, U1151, CNRS Unité mixte de recherche 8253, Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
Johanna EscoubetUnité de Sciences Translationnelles, Sanofi, Chilly-Mazarin, France; and.
Yves-Marie PersINSERM, U1183, CHU Saint Eloi, Montpellier, France.
Christian JorgensenINSERM, U1183, CHU Saint Eloi, Montpellier, France.
Florence ApparaillyINSERM, U1183, CHU Saint Eloi, Montpellier, France.
Inserm · FRDélégation Paris 5 · FRLeibniz Association · DESanofi (France) · FRCentre National de la Recherche Scientifique · FRCharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic changes drive monocyte differentiation and fate. Although abnormal mitochondria metabolism and innate immune responses participate in the pathogenesis of many inflammatory disorders, molecular events regulating mitochondrial activity to control life and death in monocytes remain poorly understood. We show here that, in human monocytes, microRNA-125b (miR-125b) attenuates the mitochondrial respiration through the silencing of the BH3-only proapoptotic protein BIK and promotes the elongation of the mitochondrial network through the targeting of the mitochondrial fission process 1 protein MTP18, leading to apoptosis. Proinflammatory activation of monocyte-derived macrophages is associated with a concomitant increase in miR-125b expression and decrease in BIK and MTP18 expression, which lead to reduced oxidative phosphorylation and enhanced mitochondrial fusion. In a chronic inflammatory systemic disorder, CD14

Indexed as

AgedApoptosisApoptosis Regulatory ProteinsCell PolarityCell RespirationFemaleGene Expression RegulationGene SilencingHEK293 CellsHumansInflammationLipopolysaccharide ReceptorsMacrophagesMaleMembrane ProteinsMicroRNAsApoptosis Regulatory ProteinsBIK protein, humanLipopolysaccharide ReceptorsMembrane ProteinsMicroRNAsMIRN125 microRNA, humanMitochondrial ProteinsMTFP1 protein, humanToll-Like Receptor 4

Identifiers

PMID27702798
PMCPMC5335801
OpenAlexW2528461366

What OpenQuestion holds

Textmetadata
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.