Evidence map›Paper›PMID 42764291›Full record

ArticleNature communications2026

Acoustic cell patterning reveals geometry- and substrate-dependent vasculogenesis and human embryo model development.

Zhaoyi Xu, Weiping Li, Xufeng Xue, Nicholas G Schott, Chenjun Shi, Ruxin Yang, Shiyu Sun, Jeyoon Bok, Jitao Zhang, Jan P Stegemann and 2 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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Zhaoyi Xu *Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-1785-5836
Weiping Li *Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0009-0006-6410-437X
Xufeng XueDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-9379-8589
Nicholas G SchottDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Chenjun ShiDepartment of Biomedical Engineering, Michigan State University, East Lansing, MI, USA.
Ruxin YangDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.
Shiyu SunDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.
Jeyoon BokDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.
Jitao ZhangDepartment of Biomedical Engineering, Michigan State University, East Lansing, MI, USA.ORCID http://orcid.org/0000-0002-6240-0371
Jan P StegemannDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Jianping FuDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA. jpfu@umich.edu.ORCID http://orcid.org/0000-0001-9629-6739
Cheri X DengDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA. dengche6@msu.edu.ORCID http://orcid.org/0000-0002-5445-1056

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise spatial organization of cells is critical for engineering functional tissues and constructing human developmental models. Here, we report the development of acoustic cell patterning (ACP), an ultrasound-based method capable of rapidly generating spatial patterns of multiple cell types on both rigid and compliant substrates without requiring chemical or physical modification of the substrates. Spatially controlled co-patterning of human endothelial and stromal fibroblast cells through ACP reveals geometry- and substrate-dependent vascular morphogenesis. Applied to human pluripotent stem cells (hPSCs) within a microfluidic device, ACP forms neural tube-like structures exhibiting in vivo-like spatially patterned gene expression, including caudal emergence of HOXC10. ACP also generates a uniform array of hPSC clusters on soft substrates, forming epiblast-like tissues that undergo spontaneous BMP-dependent amniogenesis and primordial germ cell-like specification. These in vivo-like developmental features are not observed in structures derived from patterned hPSCs using microcontact printing on stiff substrates. Together, these results demonstrate the unique capabilities of ACP for engineering spatially organized multicellular systems and modeling early human development under conditions that better mimic in vivo environments.

Indexed as

AngiogenesisEmbryo, MammalianEmbryonic DevelopmentNeovascularization, PhysiologicAnimalsCell DifferentiationEndothelial CellsFibroblastsGene Expression Regulation, DevelopmentalHumansMicrophysiological SystemsNeural TubePluripotent Stem CellsTissue Engineering

Identifiers

PMID42764291
PMCPMC13590644

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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.