Evidence map›Paper›PMID 39869602›Full record

ArticlePLoS genetics2025

Coordinated neuron-glia regeneration through Notch signaling in planarians.

M Lucila Scimone, Bryanna Isela-Inez Canales, Patrick Aoude, Kutay D Atabay, Peter W Reddien

Abstract read
In one paragraph

Article in PLoS genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. eLife · 2025
    Article
  6. bioRxiv : the preprint server for biology · 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

5 authors.

M Lucila ScimoneHoward Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0000-0002-3226-6888
Bryanna Isela-Inez CanalesWhitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America.
Patrick AoudeWhitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0000-0003-0681-4438
Kutay D AtabayWhitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0000-0001-6920-5053
Peter W ReddienHoward Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0000-0002-5569-333X

Funding

Graduate Training in Computational and Systems BiologyT32GM087237 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BURGE, CHRISTOPHER B · 2009 to 2023
$4.6M
Stem cell and regeneration regulatory mechanisms in planariansR35GM145345 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI PETER REDDIEN · 2022 to 2026
$2.4M
NIGMS NIH HHS R35 GM145345NIGMS NIH HHS T32 GM087237
6 · The paper itself

Abstract

Some animals can regenerate large missing regions of their nervous system, requiring mechanisms to restore the pattern, numbers, and wiring of diverse neuron classes. Because injuries are unpredictable, regeneration must be accomplished from an unlimited number of starting points. Coordinated regeneration of neuron-glia architecture is thus a major challenge and remains poorly understood. In planarians, neurons and glia are regenerated from distinct progenitors. We found that planarians first regenerate neurons expressing a Delta-encoding gene, delta-2, at key positions in the central and peripheral nervous systems. Planarian glia are specified later from dispersed Notch-1-expressing mesoderm-like phagocytic progenitors. Inhibition of delta-2 or notch-1 severely reduced glia in planarians, but did not affect the specification of other phagocytic cell types. Loss of several delta-2-expressing neuron classes prevented differentiation of the glia associated with them, whereas transplantation of delta-2-expressing photoreceptor neurons was sufficient for glia formation at an ectopic location. Our results suggest a model in which patterned delta-2-expressing neurons instruct phagocytic progenitors to locally differentiate into glia, presenting a mechanism for coordinated regeneration of numbers and pattern of cell types.

Indexed as

Nerve RegenerationNeurogliaNeuronsPlanariansReceptors, NotchRegenerationAnimalsCell DifferentiationIntracellular Signaling Peptides and ProteinsMembrane ProteinsSignal Transductiondelta proteinIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, Notch

Identifiers

PMID39869602
PMCPMC11801701

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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.