Evidence map›Paper›PMID 34554089›Full record

ArticleeLife2021

Integrin α5β1 nano-presentation regulates collective keratinocyte migration independent of substrate rigidity.

Jacopo Di Russo, Jennifer L Young, Julian Wr Wegner, Timmy Steins, Horst Kessler, Joachim P Spatz

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in eLife, 2021. 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
2.1field-weighted citation impact, top 13% 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, 28 citations in OpenAlex.

  1. Article
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  6. Capped high-force integrin bond lifetimes and spacing-tuned binding frequency drive rapid fibroblast migration.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  7. Article
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  10. Substrate stress relaxation regulates monolayer fluidity and leader cell formation for collectively migrating epithelia.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. The role and regulation of integrins in cell migration and invasion.Nature reviews. Molecular cell biology · 2025
    Review
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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

6 authors at 5 institutions in 3 countries.

Jacopo Di RussoMax Planck Institute for Medical Research, Heidelberg, Germany.ORCID 0000-0001-6731-9612
Jennifer L YoungMax Planck Institute for Medical Research, Heidelberg, Germany.
Julian Wr WegnerMax Planck Institute for Medical Research, Heidelberg, Germany.
Timmy SteinsInterdisciplinary Centre for Clinical Research, Aachen, Germany.
Horst KesslerInstitute for Advance Study, Department of Chemistry, Technical University of Munich, Garching, Germany.
Joachim P SpatzMax Planck Institute for Medical Research, Heidelberg, Germany.
Max Planck Institute for Medical Research · DECenter for Clinical Research (United States) · USHeidelberg University · DENational University of Singapore · SGTechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanometer-scale properties of the extracellular matrix influence many biological processes, including cell motility. While much information is available for single-cell migration, to date, no knowledge exists on how the nanoscale presentation of extracellular matrix receptors influences collective cell migration. In wound healing, basal keratinocytes collectively migrate on a fibronectin-rich provisional basement membrane to re-epithelialize the injured skin. Among other receptors, the fibronectin receptor integrin α5β1 plays a pivotal role in this process. Using a highly specific integrin α5β1 peptidomimetic combined with nanopatterned hydrogels, we show that keratinocyte sheets regulate their migration ability at an optimal integrin α5β1 nanospacing. This efficiency relies on the effective propagation of stresses within the cell monolayer independent of substrate stiffness. For the first time, this work highlights the importance of extracellular matrix receptor nanoscale organization required for efficient tissue regeneration.

Indexed as

Cell MovementMechanotransduction, CellularNanostructuresWound HealingCell AdhesionCell Culture TechniquesCell-Matrix JunctionsCell ProliferationExtracellular MatrixFibronectinsHaCaT CellsHumansHydrogelsIntegrin alpha5beta1KeratinocytesSurface PropertiesFibronectinsHydrogelsIntegrin alpha5beta1cell biologycollective cell migrationhumanintegrin α5β1keratocytesphysics of living systemswound healing

Identifiers

PMID34554089
PMCPMC8460267
OpenAlexW3201458259

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.