Evidence map›Paper›PMID 38548890›Full record

ArticleNature cell biology2024

A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex.

Laure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, Sarah Farcy, Amandine Di Cicco, Marusa Lampic, Ryszard Wimmer, Betina Bessières, Tania Attie-Bitach, Vincent Fraisier and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Nature cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
14.4field-weighted citation impact, top 1% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Temporal Transcriptional Regulation of Human Neuronal Differentiation via Forward Programming.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  8. A low-level Cdkn1c/p57EMBO reports · 2026
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Modelling human brain development and disease with organoids.Nature reviews. Molecular cell biology · 2025
    Review
  16. Article
  17. Review
  18. Review
  19. Building the brain mosaic: an expanded view.Trends in genetics : TIG · 2024
    Review
  20. It takes two to expand the cortex.Nature cell biology · 2024
    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

14 authors at 3 institutions in 1 country.

Laure Coquand *Institut Curie, PSL Research University, CNRS UMR144, Paris, France.
Clarisse Brunet Avalos *Institut Curie, PSL Research University, CNRS UMR144, Paris, France. clarisse.brunet@curie.fr.ORCID 0000-0002-7781-004X
Anne-Sophie MacéUMR 144-Cell and Tissue Imaging Facility (PICT-IBiSA), CNRS-Institut Curie, Paris, France.
Sarah FarcyInstitut Curie, PSL Research University, CNRS UMR144, Paris, France.
Amandine Di CiccoInstitut Curie, PSL Research University, CNRS UMR144, Paris, France.
Marusa LampicInstitut Curie, PSL Research University, CNRS UMR144, Paris, France.
Ryszard WimmerInstitut Curie, PSL Research University, CNRS UMR144, Paris, France.
Betina BessièresUF Embryofœtopathologie, Hopital Necker-enfants malades, Paris, France.
Tania Attie-BitachUF Embryofœtopathologie, Hopital Necker-enfants malades, Paris, France.ORCID 0000-0002-1155-3626
Vincent FraisierUMR 144-Cell and Tissue Imaging Facility (PICT-IBiSA), CNRS-Institut Curie, Paris, France.
Pierre SensInstitut Curie, PSL Research University, CNRS UMR168, Paris, France.
Fabien GuimiotUF de Fœtopathologie - Université de Paris et Inserm UMR1141, Hôpital Robert Debré, Paris, France.ORCID 0000-0002-0811-9538
Jean-Baptiste BraultInstitut Curie, PSL Research University, CNRS UMR144, Paris, France.ORCID 0000-0001-5950-2601
Alexandre D BaffetInstitut Curie, PSL Research University, CNRS UMR144, Paris, France. alexandre.baffet@curie.fr.ORCID 0000-0001-9194-4258
Centre National de la Recherche Scientifique · FRHôpital Necker-Enfants Malades · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human neocortex has undergone strong evolutionary expansion, largely due to an increased progenitor population, the basal radial glial cells. These cells are responsible for the production of a diversity of cell types, but the successive cell fate decisions taken by individual progenitors remain unknown. Here we developed a semi-automated live/fixed correlative imaging method to map basal radial glial cell division modes in early fetal tissue and cerebral organoids. Through the live analysis of hundreds of dividing progenitors, we show that basal radial glial cells undergo abundant symmetric amplifying divisions, and frequent self-consuming direct neurogenic divisions, bypassing intermediate progenitors. These direct neurogenic divisions are more abundant in the upper part of the subventricular zone. We furthermore demonstrate asymmetric Notch activation in the self-renewing daughter cells, independently of basal fibre inheritance. Our results reveal a remarkable conservation of fate decisions in cerebral organoids, supporting their value as models of early human neurogenesis.

Indexed as

Cell LineageNeocortexNeural Stem CellsNeurogenesisOrganoidsCell DifferentiationCell DivisionCell ProliferationEpendymoglial CellsHumansReceptors, NotchReceptors, Notch

Identifiers

PMID38548890
PMCPMC11098750
OpenAlexW4393261756

What OpenQuestion 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 OpenQuestion graph.