Evidence map›Paper›PMID 31772022›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Shaping the zebrafish myotome by intertissue friction and active stress.

S Tlili, J Yin, J-F Rupprecht, M A Mendieta-Serrano, G Weissbart, N Verma, X Teng, Y Toyama, J Prost, T E Saunders

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. 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
3.9field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. The role of geometry in morphogenesis.Development (Cambridge, England) · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. A model for boundary-driven tissue morphogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Dynamic forces drive cell and organ morphology changes during embryonic development.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Regulation of intercellular viscosity by E-cadherin-dependent phosphorylation of EGFR in collective cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Review
  18. Article
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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

10 authors at 3 institutions in 2 countries.

S TliliMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
J YinMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
J-F RupprechtMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
M A Mendieta-SerranoMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
G WeissbartMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
N VermaMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
X TengMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
Y ToyamaMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
J ProstMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
T E SaundersMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore; dbsste@nus.edu.sg.
National University of Singapore · SGAgency for Science, Technology and Research · SGCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organ formation is an inherently biophysical process, requiring large-scale tissue deformations. Yet, understanding how complex organ shape emerges during development remains a major challenge. During zebrafish embryogenesis, large muscle segments, called myotomes, acquire a characteristic chevron morphology, which is believed to aid swimming. Myotome shape can be altered by perturbing muscle cell differentiation or the interaction between myotomes and surrounding tissues during morphogenesis. To disentangle the mechanisms contributing to shape formation of the myotome, we combine single-cell resolution live imaging with quantitative image analysis and theoretical modeling. We find that, soon after segmentation from the presomitic mesoderm, the future myotome spreads across the underlying tissues. The mechanical coupling between the future myotome and the surrounding tissues appears to spatially vary, effectively resulting in spatially heterogeneous friction. Using a vertex model combined with experimental validation, we show that the interplay of tissue spreading and friction is sufficient to drive the initial phase of chevron shape formation. However, local anisotropic stresses, generated during muscle cell differentiation, are necessary to reach the acute angle of the chevron in wild-type embryos. Finally, tissue plasticity is required for formation and maintenance of the chevron shape, which is mediated by orientated cellular rearrangements. Our work sheds light on how a spatiotemporal sequence of local cellular events can have a nonlocal and irreversible mechanical impact at the tissue scale, leading to robust organ shaping.

Indexed as

MusclesSomitesAnimalsBiomechanical PhenomenaCells, CulturedEmbryonic DevelopmentEmbryo, NonmammalianFrictionModels, BiologicalSingle-Cell AnalysisZebrafishorgan morphogenesissomitogenesistissue mechanicsvertex models

Identifiers

PMID31772022
PMCPMC6925982
OpenAlexW2990982084

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.