Evidence map›Paper›PMID 27523733›Full record

ArticleDevelopmental cell2016

Egf Signaling Directs Neoblast Repopulation by Regulating Asymmetric Cell Division in Planarians.

Kai Lei, Hanh Thi-Kim Vu, Ryan D Mohan, Sean A McKinney, Chris W Seidel, Richard Alexander, Kirsten Gotting, Jerry L Workman, Alejandro Sánchez Alvarado

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 106 citations in OpenAlex.

  1. Article
  2. A neuregulin-like ligand and EGF receptor underpinFrontiers in cellular and infection microbiology · 2026
    Article
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  11. Receptor Tyrosine Kinase Signaling InvolvesTropical medicine and infectious disease · 2024
    Review
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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

9 authors at 2 institutions in 1 country.

Kai LeiStowers Institute for Medical Research, Kansas City, MO 64110, USA. Electronic address: kle@stowers.org.
Hanh Thi-Kim VuStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Ryan D MohanDivision of Cell Biology and Biophysics, School of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO 64110, USA.
Sean A McKinneyStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Chris W SeidelStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Richard AlexanderStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Kirsten GottingStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Jerry L WorkmanStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Alejandro Sánchez AlvaradoStowers Institute for Medical Research, Kansas City, MO 64110, USA; Howard Hughes Medical Institute, Stowers Institute for Medical Research, Kansas City, MO 64110, USA. Electronic address: asa@stowers.org.
Stowers Institute for Medical Research · USUniversity of Missouri–Kansas City · US

Funding

Transcription regulation in chromatinR35GM118068 · NIGMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI JERRY L WORKMAN · 2016 to 2026
$4.2M
The molecular basis of planarian regenerationR37GM057260 · NIGMS · UNIVERSITY OF UTAH · PI SANCHEZ ALVARADO, ALEJANDRO · 2009 to 2018
$2.8M
The molecular basis of planarian regenerationR01GM057260 · NIGMS · UNIVERSITY OF UTAH · PI SANCHEZ ALVARADO, ALEJANDRO · 1998 to 2006
$1.7M
Analysis of metazoan SAGA complex function in gene expressionR01GM099945 · NIGMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI ABMAYR, SUSAN M, WORKMAN, JERRY L · 2012 to 2015
$1.2M
NIGMS NIH HHS R01 GM057260NIGMS NIH HHS R01 GM099945NIGMS NIH HHS R35 GM118068NIGMS NIH HHS R37 GM057260
6 · The paper itself

Abstract

A large population of proliferative stem cells (neoblasts) is required for physiological tissue homeostasis and post-injury regeneration in planarians. Recent studies indicate that survival of a few neoblasts after sublethal irradiation results in the clonal expansion of the surviving stem cells and the eventual restoration of tissue homeostasis and regenerative capacity. However, the precise mechanisms regulating the population dynamics of neoblasts remain largely unknown. Here, we uncovered a central role for epidermal growth factor (EGF) signaling during in vivo neoblast expansion mediated by Smed-egfr-3 (egfr-3) and its putative ligand Smed-neuregulin-7 (nrg-7). Furthermore, the EGF receptor-3 protein localizes asymmetrically on the cytoplasmic membrane of neoblasts, and the ratio of asymmetric to symmetric cell divisions decreases significantly in egfr-3(RNAi) worms. Our results not only provide the first molecular evidence of asymmetric stem cell divisions in planarians, but also demonstrate that EGF signaling likely functions as an essential regulator of neoblast clonal expansion.

Indexed as

AMP-Activated Protein KinasesAnimalsApoptosisAsymmetric Cell DivisionCell ProliferationDNA HelicasesEpidermal Growth FactorGenomic InstabilityHelminth ProteinsMembrane ProteinsPlanariansProtein Serine-Threonine KinasesRegenerationRNA InterferenceRNA, Small InterferingSignal TransductionAMP-Activated Protein KinasesDNA HelicasesEpidermal Growth FactorHelminth ProteinsMembrane ProteinsProtein Serine-Threonine KinasesRNA, Small Interferingepidermal growth factorextracellular signalingneoblast regenerationregenerationstem cell repopulationsublethal irradiation

Identifiers

PMID27523733
PMCPMC5511498
OpenAlexW2514318134

What OpenQuestion holds

Textmetadata
LicenceTDM
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.