Evidence map›Paper›PMID 40026208›Full record

ArticleDevelopment (Cambridge, England)2025

Mechanical strain focusing at topological defect sites in regenerating Hydra.

Yonit Maroudas-Sacks, S Suganthan, Liora Garion, Yael Ascoli-Abbina, Ariel Westfried, Noam Dori, Iris Pasvinter, Marko Popović, Kinneret Keren

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Nematic cell alignment directs calcium waves.bioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. Anisotropic stretch biases the self-organization of actin fibers in multicellular Hydra aggregates.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
  12. IsJournal of developmental biology · 2025
    Review
  13. Article
  14. Topology changes ofScience advances · 2025
    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

9 authors.

Yonit Maroudas-SacksDepartment of Physics, Technion - Israel Institute of Technology, Haifa 32000, Israel.ORCID 0009-0005-6588-7305
S SuganthanMax-Planck Institute for Physics of Complex Systems, MPI-PKS, Nothnitzer Strasse 38, Dresden 01187, Germany.ORCID 0009-0000-0215-2954
Liora GarionDepartment of Physics, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Yael Ascoli-AbbinaDepartment of Physics, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Ariel WestfriedDepartment of Physics, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Noam DoriDepartment of Physics, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Iris PasvinterDepartment of Physics, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Marko PopovićMax-Planck Institute for Physics of Complex Systems, MPI-PKS, Nothnitzer Strasse 38, Dresden 01187, Germany.ORCID 0000-0003-2360-3982
Kinneret KerenDepartment of Physics, Technion - Israel Institute of Technology, Haifa 32000, Israel.ORCID 0000-0002-2962-6977

Funding

European Research Council 819174Gordon and Betty Moore Foundation 2919.02National Science Foundation NSF-PHY-2309135
6 · The paper itself

Abstract

The formation of a new head during Hydra regeneration involves the establishment of a head organizer that functions as a signaling center and contains an aster-shaped topological defect in the organization of the supracellular actomyosin fibers. Here, we show that the future head region in regenerating tissue fragments undergoes multiple instances of extensive stretching and rupture events from the onset of regeneration. These recurring localized tissue deformations arise due to transient contractions of the supracellular ectodermal actomyosin fibers that focus mechanical strain at defect sites. We further show that stabilization of aster-shaped defects is disrupted by perturbations of the Wnt signaling pathway. We propose a closed-loop feedback mechanism promoting head organizer formation, and develop a biophysical model of regenerating Hydra tissues that incorporates a morphogen source activated by mechanical strain and an alignment interaction directing fibers along morphogen gradients. We suggest that this positive-feedback loop leads to mechanical strain focusing at defect sites, enhancing local morphogen production and promoting robust organizer formation.

Indexed as

HydraRegenerationStress, MechanicalActomyosinAnimalsModels, BiologicalWnt Signaling PathwayActomyosinActomyosin fibersHydra regenerationMechanochemical feedbackMorphogenesisTopological defects

Identifiers

PMID40026208
PMCPMC11925399

What OpenQuestion holds

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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.