Evidence map›Paper›PMID 25990241›Full record

ArticleJournal of leukocyte biology2015

Regulation of miR-24, miR-30b, and miR-142-3p during macrophage and dendritic cell differentiation potentiates innate immunity.

Jezrom B Fordham, Afsar R Naqvi, Salvador Nares

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
–field-weighted citation impact
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

65 citing papers in PubMed.

  1. Article
  2. Review
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  5. Review
  6. Review
  7. Macrophage-enriched novel functional long noncoding RNAs LRRC75A-AS1 and GAPLINC regulate polarization and innate immune responses.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  8. Article
  9. Article
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  11. Article
  12. Article
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  14. Transposon control as a checkpoint for tissue regeneration.Development (Cambridge, England) · 2022
    Article
  15. MicroRNAs in shaping the resolution phase of inflammation.Seminars in cell & developmental biology · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

5 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

3 authors.

Jezrom B FordhamDepartment of Periodontics, University of Illinois at Chicago, Chicago, Illinois, USA.
Afsar R NaqviDepartment of Periodontics, University of Illinois at Chicago, Chicago, Illinois, USA.
Salvador NaresDepartment of Periodontics, University of Illinois at Chicago, Chicago, Illinois, USA snares@uic.edu.

Funding

Functional Modulation of Myeloid Inflammatory Cells by miRNAR01DE021052 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NARES, SALVADOR · 2011 to 2015
$1.9M
NIDCR NIH HHS R01 DE021052NIDCR NIH HHS R01DE021052
6 · The paper itself

Abstract

miRNAs are ubiquitous regulators of human biology. Parallel profiling of in vitro monocyte-to-Mφ and monocyte-to-DC differentiation revealed static, convergent, and divergent expression of miRNA. Bioinformatic and network analysis of differentially expressed miRNAs implicated miR-24, miR-30b, and miR-142-3p as negative regulators of intracellular signaling pathways, triggered not only by differentiation factors (M-CSF/GM-CSF/IL-4) but also from PRRs. Manipulation of miR-24, miR-30b, and miR-142-3p expression during the differentiation of mD-Mφ and mD-DC differentiation had minimal impact on the acquisition of phenotype but significantly abrogated the ability of these cells to mount inflammatory responses to pathogen-associated stimuli. Forced expression of these miRNAs, which are down-regulated during differentiation, inhibited release of inflammatory cytokines [TNF-α, IL-12(p40), IL-6] upon stimulation with LPS. Functional analysis revealed overlapping mechanisms of inhibition, including surface expression of TLR4/CD14/MD-1 and intracellular PKCα/NF-κB activation. Potential intermediary targets of the TLR4-NF-κB axis included members of the PI3K and MAPK families and PKC isoforms. These results demonstrate the requirement of miR-24, miR-30b, and miR-142-3p down-regulation for the generation of fully functional Mφs and DCs.

Indexed as

Immunity, InnateCell DifferentiationDendritic CellsGene Expression RegulationGranulocyte-Macrophage Colony-Stimulating FactorHumansInterleukin-12 Subunit p40Interleukin-4Interleukin-6LipopolysaccharidesMacrophage Colony-Stimulating FactorMacrophagesMicroRNAsMonocytesOligonucleotide Array Sequence AnalysisSignal TransductionGranulocyte-Macrophage Colony-Stimulating FactorIL4 protein, humanIL6 protein, humanInterleukin-12 Subunit p40Interleukin-4Interleukin-6LipopolysaccharidesMacrophage Colony-Stimulating FactorMicroRNAsMIRN142 microRNA, humanMIRN24 microRNA, humanMIRN30b microRNA, humanTumor Necrosis Factor-alphacytokineTLR

Identifiers

PMID25990241
PMCPMC4501676

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.