Evidence map›Paper›PMID 30120291›Full record

ArticleScientific reports2018

Interaction of septin 7 and DOCK8 in equine lymphocytes reveals novel insights into signaling pathways associated with autoimmunity.

Melanie Schauer, Kristina J H Kleinwort, Roxane L Degroote, Carmen Wiedemann, Elisabeth Kremmer, Stefanie M Hauck, Cornelia A Deeg

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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
1.0field-weighted citation impact, top 23% 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, 15 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Melanie SchauerChair for Animal Physiology, Department of Veterinary Sciences, LMU Munich, 80539, Munich, Germany.
Kristina J H KleinwortChair for Animal Physiology, Department of Veterinary Sciences, LMU Munich, 80539, Munich, Germany.
Roxane L DegrooteChair for Animal Physiology, Department of Veterinary Sciences, LMU Munich, 80539, Munich, Germany.
Carmen WiedemannChair for Animal Physiology, Department of Veterinary Sciences, LMU Munich, 80539, Munich, Germany.
Elisabeth KremmerInstitute for Molecular Immunology, Helmholtz Center Munich, German Research Center for Environmental Health GmbH, 81377, Munich, Germany.
Stefanie M HauckResearch Unit Protein Science, Helmholtz Center Munich, German Research Center for Environmental Health GmbH, 80939, Munich, Germany.ORCID 0000-0002-1630-6827
Cornelia A DeegChair for Animal Physiology, Department of Veterinary Sciences, LMU Munich, 80539, Munich, Germany. Cornelia.Deeg@lmu.de.
Ludwig-Maximilians-Universität München · DEHelmholtz Zentrum München · DELMU Klinikum · DE

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) DE 719/4 3
6 · The paper itself

Abstract

The GTP-binding protein septin 7 is involved in various cellular processes, including cytoskeleton organization, migration and the regulation of cell shape. Septin 7 function in lymphocytes, however, is poorly characterized. Since the intracellular signaling role of septin 7 is dependent on its interaction network, interaction proteomics was applied to attain novel knowledge about septin 7 function in hematopoietic cells. Our previous finding of decreased septin 7 expression in blood-derived lymphocytes in ERU, a spontaneous animal model for autoimmune uveitis in man, extended the role of septin 7 to a potential key player in autoimmunity. Here, we revealed novel insights into septin 7 function by identification of DOCK8 as an interaction partner in primary blood-derived lymphocytes. Since DOCK8 is associated with important immune functions, our finding of significantly decreased DOCK8 expression and altered DOCK8 interaction network in ERU might explain changes in immune response and shows the contribution of DOCK8 in pathomechanisms of spontaneous autoimmune diseases. Moreover, our analyses revealed insights in DOCK8 function, by identifying the signal transducer ILK as a DOCK8 interactor in lymphocytes. Our finding of the enhanced enrichment of ILK in ERU cases indicates a deviant influence of DOCK8 on inter- and intracellular signaling in autoimmune disease.

Indexed as

AutoimmunitySignal TransductionAnimalsApoptosisAutoimmune DiseasesBiomarkersCase-Control StudiesCell Cycle ProteinsChromatography, LiquidDisease Models, AnimalGuanine Nucleotide Exchange FactorsHorsesLymphocytesLymphocyte SubsetsProtein BindingSeptinsBiomarkersCell Cycle ProteinsDOCK8 protein, humanGuanine Nucleotide Exchange FactorsSEPTIN7 protein, humanSeptins

Identifiers

PMID30120291
PMCPMC6098150
OpenAlexW2952977964

What OpenQuestion holds

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LicenceCC BY
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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.