Evidence map›Paper›PMID 40659869›Full record

ArticleNature cell biology2025

Atlas of amnion development during the first trimester of human pregnancy.

Wenqi Hu, Carmen Sancho-Serra, Carlos W Gantner, Hanna M Szafranska, Nita Solanky, Kate Metcalfe, Roser Vento-Tormo, Magdalena Zernicka-Goetz

Abstract read
In one paragraph

Article in Nature cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Primate amnion development.Development (Cambridge, England) · 2024
    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

8 authors.

Wenqi HuPlasticity and Self-Organization Group, Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.ORCID http://orcid.org/0000-0002-7934-9429
Carmen Sancho-SerraWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Carlos W GantnerMammalian Embryo and Stem Cell Group, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-0825-7786
Hanna M SzafranskaPlasticity and Self-Organization Group, Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Nita SolankyHuman Developmental Biology Resource, UCL GOS Institute of Child Health, London, UK.
Kate MetcalfeHuman Developmental Biology Resource, UCL GOS Institute of Child Health, London, UK.
Roser Vento-TormoWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Magdalena Zernicka-GoetzPlasticity and Self-Organization Group, Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA. magdaz@caltech.edu.ORCID http://orcid.org/0000-0002-7004-2471

Funding

Wellcome TrustWellcome Trust (Wellcome) (098287/Z/12/Z) (MZG)Wellcome Trust (Wellcome) 220540/Z/20/A
6 · The paper itself

Abstract

The amnion is a critical extra-embryonic structure that supports foetal development, yet its ontogeny remains poorly defined. Here, using single-cell transcriptomics, we identified major cell types and subtypes in the human amnion across the first trimester of pregnancy, broadly categorized into epithelial, mesenchymal and macrophage lineages. We uncovered epithelial-mesenchymal and epithelial-immune transitions, highlighting dynamic remodelling during early pregnancy. Our results further revealed key intercellular communication pathways, including BMP4 signalling from mesenchymal to epithelial cells and TGF-β signalling from macrophages to mesenchymal cells, suggesting coordinated interactions that drive amnion morphogenesis. In addition, integrative comparisons across humans, non-human primates and in vitro stem cell-based models reveal that stem cell-based models recapitulate various stages of amnion development, emphasizing the need for careful selection of model systems to accurately recapitulate in vivo amnion formation. Collectively, our findings provide a detailed view of amnion cellular composition and interactions, advancing our understanding of its developmental role and regenerative potential.

Indexed as

AmnionPregnancy Trimester, FirstAnimalsBone Morphogenetic Protein 4Cell LineageEpithelial CellsEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, DevelopmentalHumansMacrophagesPregnancySignal TransductionSingle-Cell AnalysisTranscriptomeTransforming Growth Factor betaBMP4 protein, humanBone Morphogenetic Protein 4Transforming Growth Factor beta

Identifiers

PMID40659869
PMCPMC12270915

What OpenQuestion holds

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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.