Evidence map›Paper›PMID 28963485›Full record

ArticleScientific reports2017

Human Amniotic Membrane Mesenchymal Stem Cells inhibit Neutrophil Extracellular Traps through TSG-6.

Fátima Sofía Magaña-Guerrero, Alfredo Domínguez-López, Pamela Martínez-Aboytes, Beatriz Buentello-Volante, Yonathan Garfias

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Equine adipose-derived stem cells modulateFrontiers in veterinary science · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. 25-hydroxyvitamin DFrontiers in immunology · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Tafazzin deficiency in mouse mesenchymal stem cells promote reprogramming of activated B lymphocytes toward immunosuppressive phenotypes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Review
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  18. Article
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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 2 countries.

Fátima Sofía Magaña-GuerreroBiología Celular y Tisular, Unidad de Investigación, Instituto de Oftalmología Fundación Conde de Valenciana, Chimalpopoca 14, Ciudad de México, 06800, Mexico.
Alfredo Domínguez-LópezBiología Celular y Tisular, Unidad de Investigación, Instituto de Oftalmología Fundación Conde de Valenciana, Chimalpopoca 14, Ciudad de México, 06800, Mexico.
Pamela Martínez-AboytesBiología Celular y Tisular, Unidad de Investigación, Instituto de Oftalmología Fundación Conde de Valenciana, Chimalpopoca 14, Ciudad de México, 06800, Mexico.
Beatriz Buentello-VolanteBiología Celular y Tisular, Unidad de Investigación, Instituto de Oftalmología Fundación Conde de Valenciana, Chimalpopoca 14, Ciudad de México, 06800, Mexico.
Yonathan GarfiasBiología Celular y Tisular, Unidad de Investigación, Instituto de Oftalmología Fundación Conde de Valenciana, Chimalpopoca 14, Ciudad de México, 06800, Mexico. yogarfias@institutodeoftalmologia.org.
Ocular Proteomics (United States) · USUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mesenchymal stem cells obtained from human amniotic membrane (hAMSC) possess immunosuppressive functions through soluble factors such as prostanoids and proteins; thus, they have been proposed to ameliorate inflammatory processes. On the other hand, activated neutrophils are cells of the first line of immune defense that are able to release extracellular traps (NETs). NETs are formed of DNA and granular components; however, the excessive release of NETs is associated with the development of autoimmune and chronic inflammatory diseases. In this study, we identified that conditioned medium (CM) from hAMSC was able to diminish NETs release, as well as the production of reactive oxygen species (ROS) and the mitochondrial membrane potential from LPS-stimulated mouse bone marrow-derived neutrophils (BMN). Interestingly, NETs inhibition, ROS levels decrease and mitochondrial membrane potential loss were reverted when LPS-stimulated murine derived BMN were exposed to the CM from hAMSC transfected with TSG-6-siRNA. Finally, rhTSG6 was able to significantly diminish NETs release in BMN. These data suggest an inhibition mechanism of NETs ROS-dependent in which TSG-6 participates. Consequently, we propose the hAMSC use as a therapeutic candidate in the treatment of inflammatory diseases in which NETs are involved.

Indexed as

Bone Marrow CellsMembrane Potential, MitochondrialNeutrophilsAdolescentAdultAmnionAnimalsCell Adhesion MoleculesCells, CulturedExtracellular TrapsFemaleHumansMesenchymal Stem CellsMiceReactive Oxygen SpeciesCell Adhesion MoleculesReactive Oxygen SpeciesTNFAIP6 protein, human

Identifiers

PMID28963485
PMCPMC5622031
OpenAlexW2758161665

What OpenQuestion holds

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Registered trials

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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.