Evidence map›Paper›PMID 32393780›Full record

ArticleNature communications2020

Immune modulation by complement receptor 3-dependent human monocyte TGF-β1-transporting vesicles.

Luke D Halder, Emeraldo A H Jo, Mohammad Z Hasan, Marta Ferreira-Gomes, Thomas Krüger, Martin Westermann, Diana I Palme, Günter Rambach, Niklas Beyersdorf, Cornelia Speth and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

38 citing papers in PubMed, 61 citations in OpenAlex.

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  15. Research (Washington, D.C.) · 2024
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  16. Review
  17. Stress Conditions Affect the Immunomodulatory Potential ofInternational journal of molecular sciences · 2023
    Article
  18. Article
  19. Review
  20. 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

15 authors at 5 institutions in 2 countries.

Luke D HalderDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.
Emeraldo A H JoDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.
Mohammad Z HasanDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.
Marta Ferreira-GomesDepartment of Cell Biology, Institute of Biochemistry and Biophysics, Friedrich Schiller University, 07745, Jena, Germany.
Thomas KrügerDepartment of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.
Martin WestermannElectron Microscopy Center, University Hospital Jena, 07743, Jena, Germany.
Diana I PalmeDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.
Günter RambachDivision of Hygiene and Medical Microbiology, Medical University of Innsbruck, A-6020, Innsbruck, Austria.
Niklas BeyersdorfInstitute for Virology and Immunobiology, University of Würzburg, 97070, Würzburg, Germany.
Cornelia SpethDivision of Hygiene and Medical Microbiology, Medical University of Innsbruck, A-6020, Innsbruck, Austria.ORCID http://orcid.org/0000-0001-5637-5993
Ilse D JacobsenResearch Group Microbial Immunology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.ORCID http://orcid.org/0000-0002-6033-9984
Olaf KniemeyerDepartment of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.
Berit JungnickelDepartment of Cell Biology, Institute of Biochemistry and Biophysics, Friedrich Schiller University, 07745, Jena, Germany.
Peter F ZipfelDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany.ORCID http://orcid.org/0000-0002-6149-2411
Christine SkerkaDepartment of Infection Biology, Leibniz Institute for Natural Product Research and Infection Biology, 07745, Jena, Germany. christine.skerka@hki-jena.de.ORCID http://orcid.org/0000-0003-2374-6473
Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) · DEFriedrich Schiller University Jena · DEInnsbruck Medical University · ATJena University Hospital · DEUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles have an important function in cellular communication. Here, we show that human and mouse monocytes release TGF-β1-transporting vesicles in response to the pathogenic fungus Candida albicans. Soluble β-glucan from C. albicans binds to complement receptor 3 (CR3, also known as CD11b/CD18) on monocytes and induces the release of TGF-β1-transporting vesicles. CR3-dependence is demonstrated using CR3-deficient (CD11b knockout) monocytes generated by CRISPR-CAS9 genome editing and isolated from CR3-deficient (CD11b knockout) mice. These vesicles reduce the pro-inflammatory response in human M1-macrophages as well as in whole blood. Binding of the vesicle-transported TGF-β1 to the TGF-β receptor inhibits IL1B transcription via the SMAD7 pathway in whole blood and induces TGFB1 transcription in endothelial cells, which is resolved upon TGF-β1 inhibition. Notably, human complement-opsonized apoptotic bodies induce production of similar TGF-β1-transporting vesicles in monocytes, suggesting that the early immune response might be suppressed through this CR3-dependent anti-inflammatory vesicle pathway.

Indexed as

ImmunomodulationAnimalsApoptosisbeta-GlucansCandida albicansDown-RegulationDynamic Light ScatteringHumansHuman Umbilical Vein Endothelial CellsInflammationInterleukin-6Macrophage-1 AntigenMacrophagesMice, Inbred C57BLModels, BiologicalMonocytesbeta-GlucansInterleukin-6Macrophage-1 AntigenTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID32393780
PMCPMC7214408
OpenAlexW3022935852

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.