Evidence map›Paper›PMID 41841400›Full record

ArticleAdvanced healthcare materials2026

The Floor-Ceiling-Chip, or 2 × 2D = Pseudo-3D-Approaching 3D Cell Morphology and Organization between Two Opposing 2D Substrates with Cell-Adhesive Protein Micropatterns.

Urandelger Tuvshindorj, Francesca Giacomini, Esra Güben Kaçmaz, Tim Ten Brink, Lorenzo Moroni, Zeinab Tahmasebi Birgani, Clemens van Blitterswijk, Pamela Habibović, Stefan Giselbrecht, Jan de Boer and 1 more

Abstract read
In one paragraph

Article in Advanced healthcare materials, 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
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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

11 authors.

Urandelger TuvshindorjMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Francesca GiacominiMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Esra Güben KaçmazMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Tim Ten BrinkMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Lorenzo MoroniMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Zeinab Tahmasebi BirganiMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Clemens van BlitterswijkMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Pamela HabibovićMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Stefan GiselbrechtMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.
Jan de BoerDepartment of Biomedical Engineering and Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, The Netherlands.
Roman TruckenmüllerMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0001-7541-525X

Funding

Dutch province of Limburg SAS-2014-00837Dutch province of Limburg SAS-2018-02477Netherlands Organization for Scientific Research 024.003.013Netherlands Organization for Scientific Research 18748Study Abroad Program of the Turkish Ministry of National Education
6 · The paper itself

Abstract

In this proof-of-concept study, we develop a novel 3D cell patterning and culture platform. The "Floor-Ceiling-Chip" (FC-Chip) simply consists of two opposing 2D substrates in the form of ion track-etched membranes, creating a pseudo-3D microenvironment for the cells between them. This allows the stimulation of both the dorsal and ventral sides of cells, thereby also eliminating the artificial polarization, for example, of stromal cells, observed in standard culture dishes and inserts. By providing the membranes with micropatterned cell-adhesive islands of varying geometries and sizes, the FC-Chip enables control over cell shape and alignment in a 3D environment. Analysis of fluorescence microscopic images reveals distinct cellular and nuclear morphology, along with perinuclear actin organization, in the on-chip cultures compared to cultures on traditional 2D substrates. Cells in the FC-Chip exhibit fewer focal adhesions, lower expression of lamin A/C, and less nuclear localization of the yes-associated protein 1. The chip demonstrates compatibility with standard biochemical assays and supports long-term cultures up to 10 days, expanding its potential applications. Overall, the early version of the FC-Chip presented here confirms the feasibility of a straightforward, accessible, and versatile future culture platform for the manipulation and modeling of cell morphology and organization in 3D.

Indexed as

Cell Culture TechniquesCell Culture Techniques, Three DimensionalAnimalsCell AdhesionCell ShapeFocal AdhesionsHumansMice3D cell culturecell morphologyion‐track etched membranesmechanotransductionprotein micropatterning

Identifiers

PMID41841400
PMCPMC13206373

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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.