Evidence map›Paper›PMID 30799071›Full record

ArticleBiophysical journal2019

The Role of Early Bioelectric Signals in the Regeneration of Planarian Anterior/Posterior Polarity.

Fallon Durant, Johanna Bischof, Chris Fields, Junji Morokuma, Joshua LaPalme, Alison Hoi, Michael Levin

Abstract read
In one paragraph

Article in Biophysical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Galvanotactic directionality of cell groups depends on group size.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Electric spiking activity in epithelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. The Multiscale Wisdom of the Body: Collective Intelligence as a Tractable Interface for Next-Generation Biomedicine.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Inter-organ communication during tissue regeneration.Development (Cambridge, England) · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

7 authors.

Fallon DurantAllen Discovery Center at Tufts University, Department of Biology, Tufts University, Medford, Massachusetts.
Johanna BischofAllen Discovery Center at Tufts University, Department of Biology, Tufts University, Medford, Massachusetts.
Chris FieldsAllen Discovery Center at Tufts University, Department of Biology, Tufts University, Medford, Massachusetts.
Junji MorokumaAllen Discovery Center at Tufts University, Department of Biology, Tufts University, Medford, Massachusetts.
Joshua LaPalmeAllen Discovery Center at Tufts University, Department of Biology, Tufts University, Medford, Massachusetts.
Alison HoiAllen Discovery Center at Tufts University, Department of Biology, Tufts University, Medford, Massachusetts.
Michael LevinAllen Discovery Center at Tufts University, Department of Biology, Tufts University, Medford, Massachusetts. Electronic address: michael.levin@tufts.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Axial patterning during planarian regeneration relies on a transcriptional circuit that confers distinct positional information on the two ends of an amputated fragment. The earliest known elements of this system begin demarcating differences between anterior and posterior wounds by 6 h postamputation. However, it is still unknown what upstream events break the axial symmetry, allowing a mutual repressor system to establish invariant, distinct biochemical states at the anterior and posterior ends. Here, we show that bioelectric signaling at 3 h is crucial for the formation of proper anterior-posterior polarity in planaria. Briefly manipulating the endogenous bioelectric state by depolarizing the injured tissue during the first 3 h of regeneration alters gene expression by 6 h postamputation and leads to a double-headed phenotype upon regeneration despite confirmed washout of ionophores from tissue. These data reveal a primary functional role for resting membrane potential taking place within the first 3 h after injury and kick-starting the downstream pattern of events that elaborate anatomy over the following 10 days. We propose a simple model of molecular-genetic mechanisms to explain how physiological events taking place immediately after injury regulate the spatial distribution of downstream gene expression and anatomy of regenerating planaria.

Indexed as

Electrophysiological PhenomenaRegenerationSignal TransductionAnimalsbeta CateninGene Expression RegulationMembrane PotentialsPlanariansbeta Catenin

Identifiers

PMID30799071
PMCPMC6401388

What OpenQuestion holds

Textmetadata
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.