Evidence map›Paper›PMID 40239657›Full record

ArticleCurrent biology : CB2025

Developmental onset of planarian whole-body regeneration depends on axis reset.

Clare L T Booth, Brian C Stevens, Clover A Stubbert, Neil T Kallgren, Ennis W Deihl, Erin L Davies

Abstract read
In one paragraph

Article in Current biology : CB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Clare L T BoothCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21704, USA; Molecular and Cellular Biology Program, University of Washington, Seattle, WA 98195, USA.
Brian C StevensCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21704, USA; Department of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA.
Clover A StubbertCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21704, USA; Molecular Biology Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Neil T KallgrenCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21704, USA.
Ennis W DeihlCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21704, USA.
Erin L DaviesCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21704, USA. Electronic address: erin.davies@nih.gov.

Funding

Mechanisms underlying the establishment of whole-body regeneration competenceZIABC012009 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DAVIES, ERIN · 2020 to 2025
$2.4M
Intramural NIH HHS ZIA BC012009
6 · The paper itself

Abstract

Regenerative abilities vary across species and developmental stages of animal life cycles. Determining mechanisms that promote or limit regeneration in certain life cycle stages may pinpoint the most critical factors for successful regeneration and suggest strategies for reverse-engineering regenerative responses in therapeutic settings. In contrast to many mammalian systems, which typically show a loss of regenerative abilities with age, planarian flatworms remain highly regenerative throughout adulthood. The robust reproductive and regenerative capabilities of the planarian Schmidtea polychroa (S. polychroa) make them an ideal model to determine when and how regeneration competence is established during development. We report that S. polychroa gradually acquires whole-body regenerative abilities during late embryonic and early juvenile stages. Anterior fragments are capable of regenerating missing trunk and tail tissues from stage 6.5 onward. By contrast, the ability of posterior fragments to make new head tissue depends on the developmental stage, tissue composition of the amputated fragment, and axial position of the cut plane. Irradiation-sensitive cells are required, but not sufficient, for the onset of head regeneration ability. We propose that regulation of the main body axis reset, specifically the ability to remake an anterior organizing center, determines when whole-body regeneration competence arises during development. Supporting this hypothesis, knockdown of the canonical Wnt pathway effector Spol-β-catenin-1, a posterior determinant, induces precocious head regeneration under conditions that are normally head regeneration-incompetent. Our results suggest that regeneration competence emerges through interactions between irradiation-sensitive cells, the cellular source of new tissue, and developing adult tissue(s) harboring axial patterning information.

Indexed as

Body PatterningPlanariansRegenerationAnimalsHelminth ProteinsHelminth Proteinsaxial polarityembryogenesisnotumplanarianregenerationSchmidtea polychroatranscriptional injury responsewnt-1Wnt pathwayβ-catenin

Identifiers

PMID40239657
PMCPMC12151775

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Registered trials

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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.