Evidence map›Paper›PMID 38514807›Full record

ArticleThe EMBO journal2024

The growth factor EPIREGULIN promotes basal progenitor cell proliferation in the developing neocortex.

Paula Cubillos, Nora Ditzer, Annika Kolodziejczyk, Gustav Schwenk, Janine Hoffmann, Theresa M Schütze, Razvan P Derihaci, Cahit Birdir, Johannes Em Köllner, Andreas Petzold and 5 more

Open access · diamondAbstract read
In one paragraph

Article in The EMBO journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
4.7field-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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Shaping the Neocortex: Radial Glia and Astrocytes in Development and Evolution.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  8. Article
  9. Article
  10. Indirect neurogenesis in space and time.Nature reviews. Neuroscience · 2024
    Review
  11. 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

15 authors at 6 institutions in 2 countries.

Paula CubillosCenter for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307, Dresden, Germany.
Nora DitzerCenter for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0002-7157-0372
Annika KolodziejczykCenter for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0003-4447-2563
Gustav SchwenkCenter for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307, Dresden, Germany.
Janine HoffmannCenter for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0002-1595-5411
Theresa M SchützeCenter for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307, Dresden, Germany.
Razvan P DerihaciDepartment of Gynecology and Obstetrics, TU Dresden, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0001-9357-5230
Cahit BirdirDepartment of Gynecology and Obstetrics, TU Dresden, 01307, Dresden, Germany.
Johannes Em KöllnerMax Planck Institute of Molecular Cell Biology and Genetics, 01307, Dresden, Germany.ORCID http://orcid.org/0009-0008-8853-6593
Andreas PetzoldDRESDEN-concept Genome Center, Center for Molecular and Cellular Bioengineering, TUD Dresden University of Technology, 01307, Dresden, Germany.
Mihail SarovMax Planck Institute of Molecular Cell Biology and Genetics, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0003-2895-4087
Ulrich MartinLeibniz Research Laboratories for Biotechnology and Artificial Organs, Department of Cardiothoracic, Transplantation and Vascular Surgery, Hannover Medical School, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0003-1058-4540
Katherine R LongCentre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, SE1 1UL, United Kingdom.ORCID http://orcid.org/0000-0003-0660-2486
Pauline WimbergerDepartment of Gynecology and Obstetrics, TU Dresden, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0002-7380-577X
Mareike AlbertCenter for Regenerative Therapies TU Dresden, TUD Dresden University of Technology, 01307, Dresden, Germany. mareike.albert@tu-dresden.de.ORCID http://orcid.org/0000-0001-9855-9344
Technische Universität Dresden · DECenter for Systems Biology Dresden · DEMax Planck Institute of Molecular Cell Biology and Genetics · DENational Center for Tumor Diseases · DEKing's College London · GBMedizinische Hochschule Hannover · DE

Funding

Bundesministerium für Bildung und Forschung (BMBF) 01EW2208Bundesministerium für Bildung und Forschung (BMBF) transCampusDeutsche Forschungsgemeinschaft (DFG) AL 2231/1-1MRC MR/S025065/1
6 · The paper itself

Abstract

Neocortex expansion during evolution is linked to higher numbers of neurons, which are thought to result from increased proliferative capacity and neurogenic potential of basal progenitor cells during development. Here, we show that EREG, encoding the growth factor EPIREGULIN, is expressed in the human developing neocortex and in gorilla cerebral organoids, but not in the mouse neocortex. Addition of EPIREGULIN to the mouse neocortex increases proliferation of basal progenitor cells, whereas EREG ablation in human cortical organoids reduces proliferation in the subventricular zone. Treatment of cortical organoids with EPIREGULIN promotes a further increase in proliferation of gorilla but not of human basal progenitor cells. EPIREGULIN competes with the epidermal growth factor (EGF) to promote proliferation, and inhibition of the EGF receptor abrogates the EPIREGULIN-mediated increase in basal progenitor cells. Finally, we identify putative cis-regulatory elements that may contribute to the observed inter-species differences in EREG expression. Our findings suggest that species-specific regulation of EPIREGULIN expression may contribute to the increased neocortex size of primates by providing a tunable pro-proliferative signal to basal progenitor cells in the subventricular zone.

Indexed as

EpiregulinNeocortexAnimalsCell ProliferationGorilla gorillaHumansIntercellular Signaling Peptides and ProteinsMicePrimatesEpiregulinEREG protein, humanIntercellular Signaling Peptides and ProteinsCortical OrganoidGene RegulationHuman NeurogenesisNeocortex EvolutionNeural Progenitor Cell

Identifiers

PMID38514807
PMCPMC11021537
OpenAlexW4393043449

What Socratic holds

Textmetadata
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 Socratic graph.