Evidence map›Paper›PMID 19491394›Full record

ArticleBlood2009

Neutrophil morphology and migration are affected by substrate elasticity.

Patrick W Oakes, Dipan C Patel, Nicole A Morin, Daniel P Zitterbart, Ben Fabry, Jonathan S Reichner, Jay X Tang

Abstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed
–field-weighted citation impact
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

110 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Measuring and Analyzing Bacterial Movement in Mucus.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Generative modeling of biological shapes and images using a probabilisticbioRxiv : the preprint server for biology · 2024
    Article
  18. Review
  19. Article
  20. Article

50 more citing papers are in PubMed but not listed here.

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.

Patrick W OakesDepartment of Physics, Brown University, Providence, RI, USA.
Dipan C Patel
Nicole A Morin
Daniel P Zitterbart
Ben Fabry
Jonathan S Reichner
Jay X Tang

Funding

Effect of Neutrophil Priming on Chemotaxis and SignalingR01GM066194 · NIGMS · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI REICHNER, JONATHAN S · 2003 to 2011
$2.4M
Neutrophil MechanosensingR21AI079582 · NIAID · RHODE ISLAND HOSPITAL · PI REICHNER, JONATHAN S · 2008 to 2009
$427k
Effect of Neutrophil Priming on Chemotaxis and SignalingR56GM066194 · NIGMS · RHODE ISLAND HOSPITAL · PI REICHNER, JONATHAN S · 2007 to 2007
$254k
NIAID NIH HHS AI079582NIAID NIH HHS R21 AI079582NIGMS NIH HHS GM066194NIGMS NIH HHS R01 GM066194NIGMS NIH HHS R56 GM066194
6 · The paper itself

Abstract

To reach sites of inflammation, neutrophils execute a series of adhesion and migration events that include transmigration through the vascular endothelium and chemotaxis through the vicinal extracellular matrix until contact is made with the point of injury or infection. These in vivo microenvironments differ in their mechanical properties. Using polyacrylamide gels of physiologically relevant elasticity in the range of 5 to 100 kPa and coated with fibronectin, we tested how neutrophil adhesion, spreading, and migration were affected by substrate stiffness. Neutrophils on the softest gels showed only small changes in spread area, whereas on the stiffest gels they showed a 3-fold increase. During adhesion and migration, the magnitudes of the distortions induced in the gel substrate were independent of substrate stiffness, corresponding to the generation of significantly larger traction stresses on the stiffer gels. Cells migrated more slowly but more persistently on stiffer substrates, which resulted in neutrophils moving greater distances over time despite their slower speeds. The largest tractions were localized to the posterior of migrating neutrophils and were independent of substrate stiffness. Finally, the phosphatidylinositol 3-kinase inhibitor LY294002 obviated the ability to sense substrate stiffness, suggesting that phosphatidylinositol 3-kinase plays a mechanistic role in neutrophil mechanosensing.

Indexed as

Cell AdhesionCell MovementChromonesElasticityEnzyme InhibitorsGelsHumansMechanotransduction, CellularMorpholinesNeutrophilsPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase Inhibitors2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneChromonesEnzyme InhibitorsGelsMorpholinesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase Inhibitors

Identifiers

PMID19491394
PMCPMC2727411

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.