Evidence map›Paper›PMID 24093566›Full record

ArticleACS nano2013

Adhesion maturation of neutrophils on nanoscopically presented platelet glycoprotein Ibα.

Sebastian Kruss, Luise Erpenbeck, Katharina Amschler, Tabea A Mundinger, Heike Boehm, Hans-Joachim Helms, Tim Friede, Robert K Andrews, Michael P Schön, Joachim P Spatz

Open access · bronzeAbstract read
In one paragraph

Article in ACS nano, 2013. 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
3.3field-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

19 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Serum and Serum Albumin InhibitFrontiers in immunology · 2019
    Article
  7. Blue and Long-Wave Ultraviolet Light InduceFrontiers in immunology · 2019
    Article
  8. Article
  9. Article
  10. Proteolytic processing of platelet receptors.Research and practice in thrombosis and haemostasis · 2018
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. High-resolution imaging of cellular dopamine efflux using a fluorescent nanosensor array.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  16. Article
  17. Article
  18. Article
  19. Nanomaterials, inflammation, and tissue engineering.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    Review
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 4 institutions in 2 countries.

Sebastian KrussDepartment of New Materials and Biosystems, Max Planck Institute for Intelligent Systems , and Institute of Physical Chemistry, Heidelberg University , Heisenbergstraße 3, Stuttgart 70569, Germany.
Luise Erpenbeck
Katharina Amschler
Tabea A Mundinger
Heike Boehm
Hans-Joachim Helms
Tim Friede
Robert K Andrews
Michael P Schön
Joachim P Spatz
Universitätsmedizin Göttingen · DEMax Planck Institute for Intelligent Systems · DEHeidelberg University · DEMonash University · AU

Funding

Nanomedicine development center for mechanobiologyPN2EY016586 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2005 to 2014
$23.0M
NEI NIH HHS PN2 EY016586
6 · The paper itself

Abstract

Neutrophilic granulocytes play a fundamental role in cardiovascular disease. They interact with platelet aggregates via the integrin Mac-1 and the platelet receptor glycoprotein Ibα (GPIbα). In vivo, GPIbα presentation is highly variable under different physiological and pathophysiological conditions. Here, we quantitatively determined the conditions for neutrophil adhesion in a biomimetic in vitro system, which allowed precise adjustment of the spacings between human GPIbα presented on the nanoscale from 60 to 200 nm. Unlike most conventional nanopatterning approaches, this method provided control over the local receptor density (spacing) rather than just the global receptor density. Under physiological flow conditions, neutrophils required a minimum spacing of GPIbα molecules to successfully adhere. In contrast, under low-flow conditions, neutrophils adhered on all tested spacings with subtle but nonlinear differences in cell response, including spreading area, spreading kinetics, adhesion maturation, and mobility. Surprisingly, Mac-1-dependent neutrophil adhesion was very robust to GPIbα density variations up to 1 order of magnitude. This complex response map indicates that neutrophil adhesion under flow and adhesion maturation are differentially regulated by GPIbα density. Our study reveals how Mac-1/GPIbα interactions govern cell adhesion and how neutrophils process the number of available surface receptors on the nanoscale. In the future, such in vitro studies can be useful to determine optimum therapeutic ranges for targeting this interaction.

Indexed as

Binding SitesBiomimeticsBlood PlateletsCell AdhesionCell MovementGoldGranulocytesHumansMetal NanoparticlesNanostructuresNanotechnologyNeutrophilsPlatelet Glycoprotein GPIb-IX ComplexPolymersSurface PropertiesTime FactorsGoldPlatelet Glycoprotein GPIb-IX ComplexPolymers

Identifiers

PMID24093566
PMCPMC4122703
OpenAlexW1979971062

What OpenQuestion holds

Textmetadata
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.