Evidence map›Paper›PMID 26267782›Full record

ArticleCell adhesion & migration2015

Cell traction in collective cell migration and morphogenesis: the chase and run mechanism.

András Szabó, Roberto Mayor

Abstract read
In one paragraph

Article in Cell adhesion & migration, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Physical models of collective cell motility: from cell to tissue.Journal of physics D: Applied physics · 2017
    Article
  10. Modelling collective cell migration of neural crest.Current opinion in cell biology · 2016
    Review
  11. The front and rear of collective cell migration.Nature reviews. Molecular cell biology · 2016
    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

2 authors.

András Szabóa Department of Cell and Developmental Biology ; University College London ; London UK.
Roberto Mayora Department of Cell and Developmental Biology ; University College London ; London UK.

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MR/M010465/1Wellcome Trust
6 · The paper itself

Abstract

Directional collective cell migration plays an important role in development, physiology, and disease. An increasing number of studies revealed key aspects of how cells coordinate their movement through distances surpassing several cell diameters. While physical modeling and measurements of forces during collective cell movements helped to reveal key mechanisms, most of these studies focus on tightly connected epithelial cultures. Less is known about collective migration of mesenchymal cells. A typical example of such behavior is the migration of the neural crest cells, which migrate large distances as a group. A recent study revealed that this persistent migration is aided by the interaction between the neural crest and the neighboring placode cells, whereby neural crest chase the placodes via chemotaxis, but upon contact both populations undergo contact inhibition of locomotion and a rapid reorganization of cellular traction. The resulting asymmetric traction field of the placodes forces them to run away from the chasers. We argue that this chase and run interaction may not be specific only to the neural crest system, but could serve as the underlying mechanism for several morphogenetic processes involving collective cell migration.

Indexed as

AnimalsCell CommunicationCell MovementChemotaxisEpitheliumMesodermMorphogenesisNeural Crestcell tractionchemotaxiscollective cell migrationcontact inhibition of locomotionmesenchymal cell migrationmorphogenesisN-Cadherinneural crestplacodesRac1

Identifiers

PMID26267782
PMCPMC4955368

What OpenQuestion holds

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Registered trials

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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.