Evidence map›Paper›PMID 41540620›Full record

ArticleSmall methods2026

Rapid Generation of Fusable Cell Beads for Multi-Scale Human Living Materials Assembly.

Beatriz S Moura, Maria V Monteiro, Joana F Soeiro, Nuno J O Silva, Vítor M Gaspar, João F Mano

Abstract read
In one paragraph

Article in Small methods, 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

6 authors.

Beatriz S MouraCICECO-Aveiro Institute of Materials, Department of Chemistry, University of Aveiro Campus Universitário de Santiago, Aveiro, Portugal.
Maria V MonteiroCellularis Biomodels, Pci Creative Science Park Aveiro Region, Ílhavo, Portugal.
Joana F SoeiroCICECO-Aveiro Institute of Materials, Department of Chemistry, University of Aveiro Campus Universitário de Santiago, Aveiro, Portugal.
Nuno J O SilvaCICECO-Aveiro Institute of Materials, Department of Physics, University of Aveiro Campus Universitário de Santiago, Aveiro, Portugal.
Vítor M GasparCICECO-Aveiro Institute of Materials, Department of Chemistry, University of Aveiro Campus Universitário de Santiago, Aveiro, Portugal.ORCID https://orcid.org/0000-0002-0372-2493
João F ManoCICECO-Aveiro Institute of Materials, Department of Chemistry, University of Aveiro Campus Universitário de Santiago, Aveiro, Portugal.ORCID https://orcid.org/0000-0002-2342-3765

Funding

FCT/MEC (PIDDAC)H2020 European Research Council H2020-ERC-AdG-883370Project CICECO-Aveiro Institute of Materials LA/P/0006/2020Project CICECO-Aveiro Institute of Materials UIDB/50011/2020Project CICECO-Aveiro Institute of Materials UIDP/50011/2020
6 · The paper itself

Abstract

Three-dimensional self-assembled cellular aggregates, such as spheroids, provide unique building blocks for bottom-up tissue engineering and in vitro disease modeling. Nevertheless, traditional spheroid production methods require prolonged cell aggregation times and are highly dependent on cell type, requiring frequent optimization steps. Additionally, spheroids' size is dependent on their cell density, preventing a control over their final volume. Herein, a methodology combining metabolic glycoengineering and click chemistry with superhydrophobic surfaces is described to rapidly create spherically structured living bead units, that can surpass the fabrication constraints of conventional spheroids. Compared to spheroids produced in low attachment settings, the living beads comprising various cell types (i.e., stem, endothelial, and cancer cells) are rapidly produced and demonstrate enhanced cell viability and cell spreading over 14 days, while maintaining principal spheroid characteristics, namely the fusion into multi-scale living materials and cellular migration capabilities. In addition, this methodology enables the production of living beads with controlled size, independently of cell density, overcoming a key limitation of current spheroid production methods. The enhanced reproducibility, reduced cell assembly time, and improved handling make these spherically structured living beads a valuable alternative, with broad application in bottom-up tissue engineering approaches and disease modeling applications.

Indexed as

MicrospheresSpheroids, CellularTissue EngineeringCell Culture TechniquesCell MovementCell SurvivalClick ChemistryHumansbottom‐up assemblycellgel beadshierarchical constructsliving materialsmetabolic glycoengineering

Identifiers

PMID41540620
PMCPMC12929925

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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.