Evidence map›Paper›PMID 26637426›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2016

Identification and characterization of a unique role for EDB fibronectin in phagocytosis.

Sabrina Kraft, Verena Klemis, Carla Sens, Thorsten Lenhard, Christian Jacobi, Yvonne Samstag, Guido Wabnitz, Michael Kirschfink, Reinhard Wallich, G Maria Hänsch and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  6. Epigenetic regulation and targeting of ECM for cancer therapy.American journal of physiology. Cell physiology · 2022
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  16. α5β1 integrin mediates pulmonary epithelial cyst formation.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Article
  17. 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

11 authors at 3 institutions in 1 country.

Sabrina KraftMax-Planck Institute of Biochemistry, 82152, Martinsried, Germany.
Verena KlemisMax-Planck Institute of Biochemistry, 82152, Martinsried, Germany.
Carla SensMax-Planck Institute of Biochemistry, 82152, Martinsried, Germany.
Thorsten LenhardDepartment of Neurology, University of Heidelberg, 69120, Heidelberg, Germany.
Christian JacobiDepartment of Neurology, University of Heidelberg, 69120, Heidelberg, Germany.
Yvonne SamstagInstitute of Immunology, University of Heidelberg, 69120, Heidelberg, Germany.
Guido WabnitzInstitute of Immunology, University of Heidelberg, 69120, Heidelberg, Germany.
Michael KirschfinkInstitute of Immunology, University of Heidelberg, 69120, Heidelberg, Germany.
Reinhard WallichInstitute of Immunology, University of Heidelberg, 69120, Heidelberg, Germany.
G Maria HänschInstitute of Immunology, University of Heidelberg, 69120, Heidelberg, Germany.
Inaam A NakchbandiMax-Planck Institute of Biochemistry, 82152, Martinsried, Germany. inaam.nakchbandi@immu.uni-heidelberg.de.
Heidelberg University · DEKrankenhaus Nordwest · DEMax Planck Institute of Biochemistry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledPlasma fibronectin is a circulating protein that facilitates phagocytosis by connecting bacteria to immune cells. A fibronectin isoform, which includes a sequence of 90 AA called extra-domain B (EDB), is synthesized de novo at the messenger RNA (mRNA) level in immune cells, but the reason for its expression remains elusive. We detected an 80-fold increase in EDB-containing fibronectin in the cerebrospinal fluid of patients with bacterial meningitis that was most pronounced in staphylococcal infections. A role for this isoform in phagocytosis was further suggested by enhanced EDB fibronectin release after internalization of Staphylococcus aureus in vitro. Using transgenic mouse models, we established that immune cell production of fibronectin contributes to phagocytosis, more so than circulating plasma fibronectin, and that accentuated release of EDB-containing fibronectin by immune cells improved phagocytosis. In line with this, administration of EDB fibronectin enhanced in vitro phagocytosis to a larger extent than plasma fibronectin. This enhancement was mediated by αvβ3 integrin as shown using inhibitors or cells from β3 integrin knockout mice. Thus, we identified both a novel function for EDB fibronectin in augmenting phagocytosis over circulating plasma fibronectin, as well as the mediating receptor. Our data also establish for the first time, a direct role for β3 integrin in bacterial phagocytosis in mammals. KEY MESSAGES: • Fibronectin containing an extra domain called EDB is released in bacterial meningitis. • EDB-containing fibronectin enhances phagocytosis more than plasma fibronectin. • The enhancement is mediated by activation of αvβ3 integrin in the presence of EDB.

Indexed as

PhagocytosisProtein Interaction Domains and MotifsActinsAnimalsCase-Control StudiesFibronectinsGene ExpressionHumansImmunohistochemistryIntegrin beta3Meningitis, BacterialMiceMice, TransgenicProtein BindingProtein MultimerizationSignal TransductionActinsFibronectinsIntegrin beta3Bacterial infectionCirculationEDBEIIIBFibronectinInnate immunityPhagocytosisPlasma fibronectinαvβ3 integrin

Identifiers

PMID26637426
PMCPMC4856727
OpenAlexW2181412539

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.