Evidence map›Paper›PMID 34686603›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

TLR or NOD receptor signaling skews monocyte fate decision via distinct mechanisms driven by mTOR and miR-155.

Alice Coillard, Léa Guyonnet, Alba De Juan, Adeline Cros, Elodie Segura

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Environment & health (Washington, D.C.) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Monocyte regulation by gut microbial signals.Trends in microbiology · 2023
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. 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

5 authors at 2 institutions in 1 country.

Alice CoillardINSERM U932, Institut Curie, Paris Sciences & Lettres Research University, Paris 75005, France.ORCID 0000-0001-6309-5754
Léa GuyonnetFlow Cytometry Core, Institut Curie, Paris Sciences & Lettres Research University, Paris 75005, France.
Alba De JuanINSERM U932, Institut Curie, Paris Sciences & Lettres Research University, Paris 75005, France.ORCID 0000-0003-0174-4389
Adeline CrosINSERM U932, Institut Curie, Paris Sciences & Lettres Research University, Paris 75005, France.
Elodie SeguraINSERM U932, Institut Curie, Paris Sciences & Lettres Research University, Paris 75005, France; elodie.segura@curie.fr.ORCID 0000-0003-1795-1921
Inserm · FRInstitut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monocytes are rapidly recruited to inflamed tissues where they differentiate into monocyte-derived macrophages (mo-mac) or dendritic cells (mo-DC). At infection sites, monocytes encounter a broad range of microbial motifs. How pathogen recognition impacts monocyte fate decision is unclear. Here, we show, using an in vitro model allowing the simultaneous differentiation of human mo-mac and mo-DC, that viruses promote mo-mac while Mycobacteria favor mo-DC differentiation. Mechanistically, we found that pathogen sensing through toll-like receptor (TLR) ligands increases mo-mac differentiation via mTORC1. By contrast, nucleotide-binding oligomerization domain (NOD) ligands favor mo-DC through the induction of TNF-α secretion and miR-155 expression. We confirmed these results in vivo, in mouse skin and by analyzing transcriptomic data from human individuals. Overall, our findings allow a better understanding of the molecular control of monocyte differentiation and of monocyte plasticity upon pathogen sensing.

Indexed as

Signal TransductionHumansToll-Like ReceptorsTOR Serine-Threonine KinasesMTOR protein, humanToll-Like ReceptorsTOR Serine-Threonine Kinasesdendritic cellmacrophagemonocytepathogen

Identifiers

PMID34686603
PMCPMC8639342
OpenAlexW3205279609

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.