Evidence map›Paper›PMID 35589751›Full record

ArticleNature communications2022

Topography-induced large-scale antiparallel collective migration in vascular endothelium.

Claire Leclech, David Gonzalez-Rodriguez, Aurélien Villedieu, Thévy Lok, Anne-Marie Déplanche, Abdul I Barakat

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Interactions Between Active Matters and Endogenous Fields.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Micro-Scale Topography Triggers Dynamic 3D Nuclear Deformations.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  11. Article
  12. Confined cell migration along extracellular matrix space in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Migration and division in cell monolayers on substrates with topological defects.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Article
  20. Article
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 3 institutions in 1 country.

Claire LeclechLadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.ORCID 0000-0001-9500-356X
David Gonzalez-RodriguezUniversité de Lorraine, LCP-A2MC, F-57000, Metz, France.ORCID 0000-0001-6152-2222
Aurélien VilledieuInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005, Paris, France.
Thévy LokLadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.
Anne-Marie DéplancheNantes Université, École Centrale Nantes, CNRS, LS2N, UMR 6004, F-44000, Nantes, France.
Abdul I BarakatLadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France. abdul.barakat@polytechnique.edu.ORCID 0000-0002-7551-3631
Centre National de la Recherche Scientifique · FRÉcole Centrale de Nantes · FRLaboratoire de Chimie et Physique - Approche Multi-échelle des Milieux Complexes

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Collective migration of vascular endothelial cells is central for embryonic development, angiogenesis, and wound closure. Although physical confinement of cell assemblies has been shown to elicit specific patterns of collective movement in various cell types, endothelial migration in vivo often occurs without confinement. Here we show that unconfined endothelial cell monolayers on microgroove substrates that mimic the anisotropic organization of the extracellular matrix exhibit a specific type of collective movement that takes the form of a periodic pattern of antiparallel cell streams. We further establish that the development of these streams requires intact cell-cell junctions and that stream sizes are particularly sensitive to groove depth. Finally, we show that modeling the endothelial cell sheet as an active fluid with the microgrooves acting as constraints on cell orientation predicts the occurrence of the periodic antiparallel cell streams as well as their lengths and widths. We posit that in unconfined cell assemblies, physical factors that constrain or bias cellular orientation such as anisotropic extracellular matrix cues or directed flow-derived shear forces dictate the pattern of collective cell movement.

Indexed as

Endothelial CellsEndothelium, VascularCell MovementExtracellular MatrixIntercellular Junctions

Identifiers

PMID35589751
PMCPMC9120158
OpenAlexW4280530067

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.