Evidence map›Paper›PMID 41484134›Full record

ArticleNature communications2026

3D biomimetic niche modulates embryo development in vitro.

Jia Guo, Jiawei Lyu, Zili Gao, Tan Jia, Leyun Wang, Jingxi Dong, Zhen Gu, Shen Ji, Wei Li, Hongmei Wang and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2026. 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. Mechanical cues regulateMaterials today. Bio · 2026
    Article
  4. 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

15 authors.

Jia Guo *Human Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.
Jiawei Lyu *Human Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.
Zili Gao *Human Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.
Tan Jia *Human Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.
Leyun Wang *Human Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.ORCID 0000-0003-4448-0141
Jingxi DongHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.
Zhen GuDepartment of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, P. R. China.
Shen JiHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.
Wei LiHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.ORCID 0000-0001-7864-404X
Hongmei WangHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China.ORCID 0000-0003-1603-4785
Jinglei ZhaiHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China. zhaijinglei@ioz.ac.cn.
Leqian YuHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China. leqianyu@ioz.ac.cn.ORCID 0000-0003-2060-463X
Guihai FengHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China. fenggh@ioz.ac.cn.ORCID 0000-0002-8726-1734
Qi ZhouHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China. zhouqi@ioz.ac.cn.ORCID 0000-0002-6549-9362
Qi GuHuman Organ Physiopathology Emulation System, State Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing, P. R. China. qgu@ioz.ac.cn.ORCID 0000-0001-9387-9525

Funding

China Postdoctoral Science Foundation 2025M772889National Natural Science Foundation of China (National Science Foundation of China) 32400684National Natural Science Foundation of China (National Science Foundation of China) 32501207National Natural Science Foundation of China (National Science Foundation of China) T2222029National Natural Science Foundation of China (National Science Foundation of China) U21A20396Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation) 7254546
6 · The paper itself

Abstract

Embryo development undergoes critical morphological transformations post-implantation, largely driven by the complex and dynamic microenvironment of the uterus. Despite advances, current 3D culture models inadequately recapitulate the uterine environment necessary for studying embryo-uterus interactions. In this work, we engineer a hydrogel inspired by the properties of the decidua, incorporating Matrigel to support blastocyst implantation and embryo development in vitro. Our findings reveal that embryos cultured within this hydrogel system successfully progress to an early organogenesis-like stage, including the development of first and second heart fields, mimicking natural embryogenesis. Moreover, we identify that the mechanical properties, particularly stress relaxation, play a crucial role in facilitating focal adhesion (FA) formation between the trophoblast and the hydrogel. Additionally, the degradation of the hydrogel by embryo-secreted metalloproteinases (MMP2 and MMP9) creates a favorable environment for continued embryonic growth and development. These insights contribute to a deeper understanding of how the external environment regulates embryo development and offer an enhanced approach for in vitro embryo culture.

Indexed as

BiomimeticsEmbryo Culture TechniquesEmbryonic DevelopmentAnimalsBiomimetic MaterialsBlastocystCollagenDeciduaDrug CombinationsEmbryo ImplantationEmbryo, MammalianFemaleFocal AdhesionsHydrogelsLamininMatrix Metalloproteinase 2CollagenDrug CombinationsHydrogelsLamininmatrigelMatrix Metalloproteinase 2Matrix Metalloproteinase 9Proteoglycans

Identifiers

PMID41484134
PMCPMC12868858

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.