Evidence map›Paper›PMID 34651174›Full record

ArticleDevelopment (Cambridge, England)2021

Cell-cell communication through FGF4 generates and maintains robust proportions of differentiated cell types in embryonic stem cells.

Dhruv Raina, Azra Bahadori, Angel Stanoev, Michelle Protzek, Aneta Koseska, Christian Schröter

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Information content and optimization of self-organized developmental systems.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Computational insights in cell physiology.Frontiers in systems biology · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Journey of the mouse primitive endoderm: from specification to maturation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  18. Article
  19. Article
  20. Review
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

6 authors at 1 institution in 1 country.

Dhruv RainaDepartment of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany.ORCID 0000-0003-4140-3925
Azra BahadoriDepartment of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany.
Angel StanoevDepartment of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany.ORCID 0000-0001-6478-7496
Michelle ProtzekDepartment of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany.
Aneta KoseskaDepartment of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany.
Christian SchröterDepartment of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, 44227 Dortmund, Germany.ORCID 0000-0002-8161-7568
Max Planck Institute of Molecular Physiology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During embryonic development and tissue homeostasis, reproducible proportions of differentiated cell types are specified from populations of multipotent precursor cells. Molecular mechanisms that enable both robust cell-type proportioning despite variable initial conditions in the precursor cells, and the re-establishment of these proportions upon perturbations in a developing tissue remain to be characterized. Here, we report that the differentiation of robust proportions of epiblast-like and primitive endoderm-like cells in mouse embryonic stem cell cultures emerges at the population level through cell-cell communication via a short-range fibroblast growth factor 4 (FGF4) signal. We characterize the molecular and dynamical properties of the communication mechanism and show how it controls both robust cell-type proportioning from a wide range of experimentally controlled initial conditions, as well as the autonomous re-establishment of these proportions following the isolation of one cell type. The generation and maintenance of reproducible proportions of discrete cell types is a new function for FGF signaling that might operate in a range of developing tissues.

Indexed as

AnimalsBody PatterningCell CommunicationCell DifferentiationEmbryonic DevelopmentEndodermFibroblast Growth Factor 4Germ LayersMiceMouse Embryonic Stem CellsParacrine CommunicationSignal TransductionFgf4 protein, mouseFibroblast Growth Factor 4Dynamical systemEmbryonic stem cellsEpiblastFGF signalingMousePreimplantation developmentPrimitive endoderm

Identifiers

PMID34651174
PMCPMC8602943
OpenAlexW3207290808

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.