Evidence map›Paper›PMID 31632402›Full record

ArticleFrontiers in immunology2019

Effect of Adhesion and Substrate Elasticity on Neutrophil Extracellular Trap Formation.

Luise Erpenbeck, Antonia Luise Gruhn, Galina Kudryasheva, Gökhan Günay, Daniel Meyer, Julia Busse, Elsa Neubert, Michael P Schön, Florian Rehfeldt, Sebastian Kruss

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 53 citations in OpenAlex.

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  6. Animals : an open access journal from MDPI · 2025
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  9. Shift of cell-death mechanisms in primary human neutrophils with a ruthenium photosensitizer.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2025
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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

10 authors at 2 institutions in 1 country.

Luise ErpenbeckDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen University, Göttingen, Germany.
Antonia Luise GruhnDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen University, Göttingen, Germany.
Galina KudryashevaThird Institute of Physics-Biophysics, Göttingen University, Göttingen, Germany.
Gökhan GünayDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen University, Göttingen, Germany.
Daniel MeyerDepartment of Chemistry, Institute of Physical Chemistry, Göttingen University, Göttingen, Germany.
Julia BusseDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen University, Göttingen, Germany.
Elsa NeubertDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen University, Göttingen, Germany.
Michael P SchönDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen University, Göttingen, Germany.
Florian RehfeldtThird Institute of Physics-Biophysics, Göttingen University, Göttingen, Germany.
Sebastian KrussDepartment of Chemistry, Institute of Physical Chemistry, Göttingen University, Göttingen, Germany.
University of Göttingen · DEUniversitätsmedizin Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils are the most abundant type of white blood cells. Upon stimulation, they are able to decondense and release their chromatin as neutrophil extracellular traps (NETs). This process (NETosis) is part of immune defense mechanisms but also plays an important role in many chronic and inflammatory diseases such as atherosclerosis, rheumatoid arthritis, diabetes, and cancer. For this reason, much effort has been invested into understanding biochemical signaling pathways in NETosis. However, the impact of the mechanical micro-environment and adhesion on NETosis is not well-understood. Here, we studied how adhesion and especially substrate elasticity affect NETosis. We employed polyacrylamide (PAA) gels with distinctly defined elasticities (Young's modulus

Indexed as

Immunity, InnateBiomarkersCell AdhesionElasticityExtracellular TrapsHumansImmunomodulationInflammationLipopolysaccharidesModels, BiologicalNeutrophilsPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsBiomarkersLipopolysaccharidesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase Inhibitorsadhesionimmunomodulationinflammationinnate immunityneutrophil extracellular traps (NET)neutrophil (PMN)stiffness and its variationssubstrate elasticity

Identifiers

PMID31632402
PMCPMC6781793
OpenAlexW2978119832

What OpenQuestion holds

Textmetadata
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.