Evidence map›Paper›PMID 28634370›Full record

ArticleScientific reports2017

Microbial Antigens Stimulate Metalloprotease-7 Secretion in Human B-Lymphocytes Using mTOR-Dependent and Independent Pathways.

Mohamed F Ali, Harika Dasari, Virginia P Van Keulen, Divi Cornec, George Vasmatzis, Tobias Peikert, Eva M Carmona

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. B Cells in Idiopathic Pulmonary Fibrosis: Targeting Immune Cells with Antifibrotic Agents.American journal of respiratory cell and molecular biology · 2021
    Article
  8. Observational
  9. 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

7 authors at 3 institutions in 1 country.

Mohamed F AliThoracic Diseases Research Unit, Rochester, Minnesota, 55905, United States.
Harika DasariThoracic Diseases Research Unit, Rochester, Minnesota, 55905, United States.
Virginia P Van KeulenThoracic Diseases Research Unit, Rochester, Minnesota, 55905, United States.
Divi CornecThoracic Diseases Research Unit, Rochester, Minnesota, 55905, United States.
George VasmatzisDepartment of Medicine and Biomarker Discovery, Center for Individualized Medicine Mayo Clinic and Foundation, Rochester, Minnesota, 55905, United States.
Tobias PeikertThoracic Diseases Research Unit, Rochester, Minnesota, 55905, United States.
Eva M CarmonaThoracic Diseases Research Unit, Rochester, Minnesota, 55905, United States. carmona.eva@mayo.edu.
Midwest Orthopaedic Research Foundation · USUniversity of Minnesota Rochester · USMayo Clinic · US

Funding

Modulation of host immune defense by Pneumocystis beta-glucansK08HL112849 · NHLBI · MAYO CLINIC ROCHESTER · PI CARMONA PORQUERA, EVA MARIA · 2013 to 2017
$712k
NHLBI NIH HHS K08 HL112849
6 · The paper itself

Abstract

Metalloproteinases (MMPs) contribute to tissue remodeling and acute inflammation not only by degrading extracellular matrix proteins but also by controlling the influx of chemokines through the regulation and shedding of syndecans. B-lymphocytes, in addition to their well-known function as antibody producing cells, participate in the innate immune response by secreting inflammatory cytokines and chemokines. However, there is little information about the role of B-lymphocytes in the regulation of MMPs; consequently, herein we investigated whether activated human circulating B-lymphocytes contributed to the secretion of MMPs. We demonstrate that B-lymphocytes activated by un-methylated CpG motifs, found in bacterial DNA, and β-glucans, found in the cell wall of fungi, both induced MMP-7. Interestingly, while CpG-stimulated cells activated the mTOR pathway via TLR9 receptor to induced MMP-7, β-glucan-stimulated cells were mTOR-independent and used Dectin-1 receptor. B-lymphocytes did not seem to have a major role in the secretion of tissue inhibitors of metalloproteinases (TIMPs). However, secreted MMP-7 participated in the shedding of Syndecan-4 from the surface of B-lymphocytes. In conclusion, circulating human B-lymphocytes contribute to the regulation of the innate immune system by participating in the secretion of MMP-7 which in turn is important for the shedding of Syndecan-4 in response to infectious stimuli.

Indexed as

Signal TransductionAntigensbeta-GlucansB-LymphocytesHumansLeukocytesMatrix Metalloproteinase 7Matrix MetalloproteinasesReceptors, Antigen, B-CellTissue Inhibitor of MetalloproteinasesToll-Like ReceptorsTOR Serine-Threonine KinasesAntigensbeta-GlucansMatrix Metalloproteinase 7Matrix MetalloproteinasesMTOR protein, humanReceptors, Antigen, B-CellTissue Inhibitor of MetalloproteinasesToll-Like ReceptorsTOR Serine-Threonine Kinases

Identifiers

PMID28634370
PMCPMC5478602
OpenAlexW2632272396

What OpenQuestion holds

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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.