Evidence map›Paper›PMID 35165417›Full record

ArticleNature cell biology2022

Rear traction forces drive adherent tissue migration in vivo.

Naoya Yamaguchi, Ziyi Zhang, Teseo Schneider, Biran Wang, Daniele Panozzo, Holger Knaut

Abstract readVideo-Audio Media
In one paragraph

Article in Nature cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Collective migration modes in development, tissue repair and cancer.Nature reviews. Molecular cell biology · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Sensing the force in living embryos.Nature materials · 2024
    Article
  18. Measurement of adhesion and traction of cells at high yield reveals an energetic ratchet operating during nephron condensation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  19. Article
  20. Field Guide to Traction Force Microscopy.Cellular and molecular bioengineering · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Naoya YamaguchiSkirball Institute of Biomolecular Medicine, New York University Grossman School of Medicine, New York, NY, USA.
Ziyi ZhangCourant Institute of Mathematical Sciences, New York University, New York, NY, USA.
Teseo SchneiderCourant Institute of Mathematical Sciences, New York University, New York, NY, USA.ORCID http://orcid.org/0000-0002-5969-636X
Biran WangMolecular Cytology Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0001-6637-6156
Daniele PanozzoCourant Institute of Mathematical Sciences, New York University, New York, NY, USA. panozzo@nyu.edu.ORCID http://orcid.org/0000-0003-1183-2454
Holger KnautSkirball Institute of Biomolecular Medicine, New York University Grossman School of Medicine, New York, NY, USA. holger.knaut@med.nyu.edu.ORCID http://orcid.org/0000-0002-8399-8720

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Biomechanics of Tissue MotilityR01NS119449 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KNAUT, HOLGER · 2021 to 2025
$2.4M
Molecular and Cellular Control of Collective Cell Migration.R01NS102322 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KNAUT, HOLGER · 2018 to 2022
$2.4M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016087NINDS NIH HHS R01 NS102322NINDS NIH HHS R01 NS119449
6 · The paper itself

Abstract

During animal embryogenesis, homeostasis and disease, tissues push and pull on their surroundings to move forward. Although the force-generating machinery is known, it is unknown how tissues exert physical stresses on their substrate to generate motion in vivo. Here, we identify the force transmission machinery, the substrate and the stresses that a tissue, the zebrafish posterior lateral line primordium, generates during its migration. We find that the primordium couples actin flow through integrins to the basement membrane for forward movement. Talin- and integrin-mediated coupling is required for efficient migration, and its loss is partially compensated for by increased actin flow. Using Embryogram, an approach to measure stresses in vivo, we show that the rear of the primordium exerts higher stresses than the front, which suggests that this tissue pushes itself forward with its back. This unexpected strategy probably also underlies the motion of other tissues in animals.

Indexed as

ChemotaxisMechanotransduction, CellularActinsAnimalsAnimals, Genetically ModifiedBasement MembraneChemokine CXCL12Embryo, NonmammalianGene Expression Regulation, DevelopmentalIntegrinsMorphogenesisReceptors, CXCR4Stress, MechanicalTalinTime FactorsZebrafishActinsChemokine CXCL12cxcl12a protein, zebrafishCXCR4b protein, zebrafishIntegrinsReceptors, CXCR4Talintln1 protein, zebrafishZebrafish Proteins

Identifiers

PMID35165417
PMCPMC8868490

What OpenQuestion holds

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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.