Evidence map›Paper›PMID 40011454›Full record

ArticleNature communications2025

ETVs dictate hPSC differentiation by tuning biophysical properties.

Natalia M Ziojła, Magdalena Socha, M Cecilia Guerra, Dorota Kizewska, Katarzyna Blaszczyk, Edyta Urbaniak, Sara Henry, Malgorzata Grabowska, Kathy K Niakan, Aryeh Warmflash and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. 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

11 authors.

Natalia M Ziojła *Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.ORCID http://orcid.org/0000-0001-6439-8466
Magdalena Socha *Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.ORCID http://orcid.org/0000-0002-0767-7511
M Cecilia GuerraDepartment of Biosciences, Rice University, Houston, TX, USA.
Dorota KizewskaInstitute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Katarzyna BlaszczykInstitute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Edyta UrbaniakInstitute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Sara HenryInstitute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.
Malgorzata GrabowskaInstitute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland.ORCID http://orcid.org/0000-0002-2711-1910
Kathy K NiakanThe Loke Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-1646-4734
Aryeh WarmflashDepartment of Biosciences, Rice University, Houston, TX, USA.
Malgorzata BorowiakInstitute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznan, Poland. malbor3@amu.edu.pl.ORCID http://orcid.org/0000-0002-5829-1213

Funding

Signaling dynamics in the control of ectoderm patterning and morphogenesisR35GM149328 · NIGMS · RICE UNIVERSITY · PI Aryeh Warmflash · 2023 to 2026
$1.5M
Narodowe Centrum Nauki (National Science Centre) 2019/33/B/NZ3/01226Narodowe Centrum Nauki (National Science Centre) 2020/37/B/NZ3/01917Narodowe Centrum Nauki (National Science Centre) UMO-2015/19/P/NZ3/03452NIGMS NIH HHS R35 GM149328NSF | BIO | Division of Molecular and Cellular Biosciences (MCB) 2135296U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences (NCATS) 5R35GM149328Wellcome TrustWellcome Trust (Wellcome) 221856/Z/20/Z
6 · The paper itself

Abstract

Stem cells maintain a dynamic dialog with their niche, integrating biochemical and biophysical cues to modulate cellular behavior. Yet, the transcriptional networks that regulate cellular biophysical properties remain poorly defined. Here, we leverage human pluripotent stem cells (hPSCs) and two morphogenesis models - gastruloids and pancreatic differentiation - to establish ETV transcription factors as critical regulators of biophysical parameters and lineage commitment. Genetic ablation of ETV1 or ETV1/ETV4/ETV5 in hPSCs enhances cell-cell and cell-ECM adhesion, leading to aberrant multilineage differentiation including disrupted germ-layer organization, ectoderm loss, and extraembryonic cell overgrowth in gastruloids. Furthermore, ETV1 loss abolishes pancreatic progenitor formation. Single-cell RNA sequencing and follow-up assays reveal dysregulated mechanotransduction via the PI3K/AKT signaling. Our findings highlight the importance of transcriptional control over cell biophysical properties and suggest that manipulating these properties may improve in vitro cell and tissue engineering strategies.

Indexed as

Cell DifferentiationDNA-Binding ProteinsPluripotent Stem CellsTranscription FactorsAnimalsBiophysical PhenomenaCell AdhesionCell LineageHumansMechanotransduction, CellularMicePancreasPhosphatidylinositol 3-KinasesSignal TransductionDNA-Binding ProteinsPhosphatidylinositol 3-KinasesTranscription Factors

Identifiers

PMID40011454
PMCPMC11865489

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Registered trials

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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.