Evidence map›Paper›PMID 25181349›Full record

ArticlePloS one2014

Directional collective cell migration emerges as a property of cell interactions.

Mae L Woods, Carlos Carmona-Fontaine, Chris P Barnes, Iain D Couzin, Roberto Mayor, Karen M Page

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

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  7. Review
  8. Rules of collective migration: from the wildebeest to the neural crest.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
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  20. Physical models of collective cell motility: from cell to tissue.Journal of physics D: Applied physics · 2017
    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.

Mae L WoodsCentre for Mathematics and Physics in the Life Sciences and Experimental Biology, University College London, London, United Kingdom; Department of Cell and Developmental Biology, University College London, London, United Kingdom; Department of Mathematics, University College London, London, United Kingdom.
Carlos Carmona-FontaineDepartment of Cell and Developmental Biology, University College London, London, United Kingdom.
Chris P BarnesDepartment of Cell and Developmental Biology, University College London, London, United Kingdom.
Iain D CouzinDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, New Jersey, United States of America.
Roberto MayorDepartment of Cell and Developmental Biology, University College London, London, United Kingdom.
Karen M PageCentre for Mathematics and Physics in the Life Sciences and Experimental Biology, University College London, London, United Kingdom; Department of Mathematics, University College London, London, United Kingdom.

Funding

Medical Research Council MR/J000655/1Wellcome Trust
6 · The paper itself

Abstract

Collective cell migration is a fundamental process, occurring during embryogenesis and cancer metastasis. Neural crest cells exhibit such coordinated migration, where aberrant motion can lead to fatality or dysfunction of the embryo. Migration involves at least two complementary mechanisms: contact inhibition of locomotion (a repulsive interaction corresponding to a directional change of migration upon contact with a reciprocating cell), and co-attraction (a mutual chemoattraction mechanism). Here, we develop and employ a parameterized discrete element model of neural crest cells, to investigate how these mechanisms contribute to long-range directional migration during development. Motion is characterized using a coherence parameter and the time taken to reach, collectively, a target location. The simulated cell group is shown to switch from a diffusive to a persistent state as the response-rate to co-attraction is increased. Furthermore, the model predicts that when co-attraction is inhibited, neural crest cells can migrate into restrictive regions. Indeed, inhibition of co-attraction in vivo and in vitro leads to cell invasion into restrictive areas, confirming the prediction of the model. This suggests that the interplay between the complementary mechanisms may contribute to guidance of the neural crest. We conclude that directional migration is a system property and does not require action of external chemoattractants.

Indexed as

Cell CommunicationCell MovementAnimalsCalibrationContact InhibitionModels, BiologicalTime FactorsXenopus

Identifiers

PMID25181349
PMCPMC4152153

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.