Evidence map›Paper›PMID 30235245›Full record

ArticlePloS one2018

Evaluation of surfactant proteins A, B, C, and D in articular cartilage, synovial membrane and synovial fluid of healthy as well as patients with osteoarthritis and rheumatoid arthritis.

Nadine Hartjen, Lars Bräuer, Beate Reiß, Horst Claassen, Stephanie Beileke, Fabian Garreis, Sebastian Hoogeboom, Michael Tsokos, Saskia Etzold, Brigitte Müller-Hilke and 5 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. 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

15 authors at 6 institutions in 2 countries.

Nadine HartjenInstitute of Functional and Clinical Anatomy, Friedrich Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Lars BräuerInstitute of Functional and Clinical Anatomy, Friedrich Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Beate ReißInstitute of Anatomy and Cell Biology, Martin Luther University Halle-Wittenberg (MLU), Halle (Saale), Germany.
Horst ClaassenInstitute of Anatomy and Cell Biology, Martin Luther University Halle-Wittenberg (MLU), Halle (Saale), Germany.
Stephanie BeilekeInstitute of Functional and Clinical Anatomy, Friedrich Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Fabian GarreisInstitute of Functional and Clinical Anatomy, Friedrich Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Sebastian HoogeboomFraunhofer Institute for Supply Chain Services SCS, Nürnberg, Germany.
Michael TsokosInstitute of Legal Medicine and Forensic Sciences, Charité University Medicine Berlin, Berlin Germany.
Saskia EtzoldInstitute of Legal Medicine and Forensic Sciences, Charité University Medicine Berlin, Berlin Germany.
Brigitte Müller-HilkeInstitute of Immunology, University of Rostock, Rostock, Germany.
Kolja GelseDepartment of Trauma Surgery, Friedrich Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Thomas MüllerDepartment of child and adolescent medicine, Pediatrics I, Pediatric Rheumatology, University of Halle-Wittenberg, Children's Hospital, Martin Luther University Halle-Wittenberg (MLU), Halle (Saale), Germany.
Mary B GoldringDepartment of Cell and Developmental Biology, Weill Cornell Medical College, New York, New York, United States of America.
Friedrich PaulsenInstitute of Functional and Clinical Anatomy, Friedrich Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Martin SchichtInstitute of Functional and Clinical Anatomy, Friedrich Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.ORCID 0000-0001-5155-5477
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEMartin Luther University Halle-Wittenberg · DECharité - Universitätsmedizin Berlin · DEFraunhofer Center for Applied Research on Supply Chain Services · DEHospital for Special Surgery · USUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSurfactant Proteins (SPs) are well known from lung and form, along with phospholipids, a surface-active-layer at the liquid-air-interface of the alveolar lining. They play a major protective role by lowering surface tension, activating innate and adaptive immune defense at the lung mucosal interface, especially during infection. We analyzed the regulation of SPs in human and mouse articular chondrocytes, synoviocytes, and synovial fluid under healthy and inflammatory conditions, as well as in tissues of patients suffering from osteoarthritis and rheumatoid arthritis.

methodsImmunohistochemistry, RT-PCR, qRT-PCR, ELISA, Western blotting were performed in cell cultures and tissue samples to determine localization, regulation, and concentration of SPs.

resultsAll four SPs, were expressed by healthy human and mouse articular chondrocytes and synoviocytes and were also present in synovial fluid. Treatment with inflammatory mediators like IL-1β and TNF-α led to short-term upregulation of individual SPs in vitro. In tissues from patients with osteoarthritis and rheumatoid arthritis, protein levels of all four SPs increased significantly compared to the controls used.

conclusionThese results show the distribution and amount of SPs in tissues of articular joints. They are produced by chondrocytes and synoviocytes and occur in measurable amounts in synovial fluid. All four SPs seem to be differently regulated under pathologic conditions. Their physiological functions in lowering surface tension and immune defense need further elucidation and make them potential candidates for therapeutic intervention.

Indexed as

AdolescentAdultAgedAged, 80 and overArthritis, RheumatoidCartilage, ArticularCell Line, TransformedFemaleHumansMaleMiddle AgedOsteoarthritisPulmonary Surfactant-Associated Protein APulmonary Surfactant-Associated Protein BPulmonary Surfactant-Associated Protein CPulmonary Surfactant-Associated Protein DPulmonary Surfactant-Associated Protein APulmonary Surfactant-Associated Protein BPulmonary Surfactant-Associated Protein CPulmonary Surfactant-Associated Protein D

Identifiers

PMID30235245
PMCPMC6147433
OpenAlexW2890375707

What OpenQuestion holds

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LicenceCC BY
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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.