Evidence map›Paper›PMID 36306780›Full record

ArticleStem cell reports2022

Stabilization of cell-cell adhesions prevents symmetry breaking and locks in pluripotency in 3D gastruloids.

Federica Cermola, Filomena Amoroso, Federica Saracino, Eduardo Ibello, Dario De Cesare, Annalisa Fico, Gilda Cobellis, Enrica Scalera, Costanza Casiraghi, Cristina D'Aniello and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 14% 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, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. N2B27 media formulations influence gastruloid development.Development (Cambridge, England) · 2025
    Article
  6. Article
  7. Review
  8. 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

12 authors at 3 institutions in 1 country.

Federica CermolaStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy.
Filomena AmorosoStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy; Department of Precision Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.
Federica SaracinoStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy.
Eduardo IbelloStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy; Department of Precision Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.
Dario De CesareStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy.
Annalisa FicoStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy.
Gilda CobellisDepartment of Precision Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.
Enrica ScaleraPharmacology and Toxicology Department, Corporate Pre-clinical R&D, Chiesi, Parma, Italy.
Costanza CasiraghiPharmacology and Toxicology Department, Corporate Pre-clinical R&D, Chiesi, Parma, Italy.
Cristina D'AnielloStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy.
Eduardo Jorge PatriarcaStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy. Electronic address: eduardo.patriarca@igb.cnr.it.
Gabriella MinchiottiStem Cell Fate Laboratory, Institute of Genetics and Biophysics "A. Buzzati Traverso", CNR, Naples, Italy. Electronic address: gabriella.minchiotti@igb.cnr.it.
Institute of Genetics and Biophysics · ITUniversity of Campania "Luigi Vanvitelli" · ITChiesi (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

3D embryonic stem cell (ESC) aggregates self-organize into embryo-like structures named gastruloids that recapitulate the axial organization of post-implantation embryos. Crucial in this process is the symmetry-breaking event that leads to the emergence of asymmetry and spatially ordered structures from homogeneous cell aggregates. Here, we show that budesonide, a glucocorticoid drug widely used to treat asthma, prevents ESC aggregates to break symmetry. Mechanistically, the effect of budesonide is glucocorticoid receptor independent. RNA sequencing and lineage fate analysis reveal that budesonide counteracts exit from pluripotency and modifies the expression of a large set of genes associated with cell migration, A-P axis formation, and WNT signaling. This correlates with reduced phenotypic and molecular cell heterogeneity, persistence of E-CADHERIN at the cell-cell interface, and cell aggregate compaction. Our findings reveal that cell-cell adhesion properties control symmetry breaking and cell fate transition in 3D gastruloids and suggest a potential adverse effect of budesonide on embryo development.

Indexed as

Embryo, MammalianEmbryonic Stem CellsBudesonideCell AdhesionEmbryonic DevelopmentBudesonide3D gastruloidsbudesonidecell-cell adhesionE-CADHERINglucocorticoid receptorglucocorticoidslocomotionpluripotencysymmetry breakingWNT signaling

Identifiers

PMID36306780
PMCPMC9669408
OpenAlexW4307447040

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.