Evidence map›Paper›PMID 23735560›Full record

ArticlePhysical biology2013

Follow-the-leader cell migration requires biased cell-cell contact and local microenvironmental signals.

Michelle L Wynn, Paul Rupp, Paul A Trainor, Santiago Schnell, Paul M Kulesa

Abstract read
In one paragraph

Article in Physical biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Quantitative Analysis of Directional Neural Crest Cell Migration.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Article
  7. Article
  8. Review
  9. Embryonic Chicken (Comparative medicine · 2019
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Modelling collective cell migration of neural crest.Current opinion in cell biology · 2016
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Michelle L WynnDepartment of Internal Medicine, Division of Hematology and Oncology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
Paul Rupp
Paul A Trainor
Santiago Schnell
Paul M Kulesa
Stowers Institute for Medical Research · USUniversity of Michigan–Ann Arbor · USUniversity of Kansas · US

Funding

MSM - Multiscale Studies of Segmentation in Vertebrate *R01GM076692 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI GLAZIER, JAMES ALEXANDER, STERN, CLAUDIO D · 2005 to 2015
$5.5M
Intrinsic and extrinsic regulation of cranial mesodermR01DE016082 · NIDCR · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI TRAINOR, PAUL · 2004 to 2014
$3.9M
Proteogenomics of Cancer Training ProgramT32CA140044 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAO, ARVIND, SARTOR, MAUREEN AGNES · 2010 to 2024
$3.9M
In Vivo Analysis of the Mechanisms of Neural Crest MigrationR01HD057922 · NICHD · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI KULESA, PAUL · 2008 to 2012
$1.7M
NCI NIH HHS T32 CA140044NICHD NIH HHS R01 HD057922NIDCR NIH HHS R01 DE016082NIGMS NIH HHS R01 GM076692
6 · The paper itself

Abstract

Directed cell migration often involves at least two types of cell motility that include multicellular streaming and chain migration. However, what is unclear is how cell contact dynamics and the distinct microenvironments through which cells travel influence the selection of one migratory mode or the other. The embryonic and highly invasive neural crest (NC) are an excellent model system to study this question since NC cells have been observed in vivo to display both of these types of cell motility. Here, we present data from tissue transplantation experiments in chick and in silico modeling that test our hypothesis that cell contact dynamics with each other and the microenvironment promote and sustain either multicellular stream or chain migration. We show that when premigratory cranial NC cells (at the pre-otic level) are transplanted into a more caudal region in the head (at the post-otic level), cells alter their characteristic stream behavior and migrate in chains. Similarly, post-otic NC cells migrate in streams after transplantation into the pre-otic hindbrain, suggesting that local microenvironmental signals dictate the mode of NC cell migration. Simulations of an agent-based model (ABM) that integrates the NC cell behavioral data predict that chain migration critically depends on the interplay of biased cell-cell contact and local microenvironment signals. Together, this integrated modeling and experimental approach suggests new experiments and offers a powerful tool to examine mechanisms that underlie complex cell migration patterns.

Indexed as

Cell CommunicationCell MovementAnimalsChick EmbryoChickensComputer SimulationExtracellular SpaceModels, BiologicalNeural Crest

Identifiers

PMID23735560
PMCPMC3756809
OpenAlexW2004878794

What OpenQuestion holds

Textmetadata
LicenceTDM
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.