Evidence map›Paper›PMID 41580917›Full record

ArticleAdvanced healthcare materials2026

A New 3D Colon on a Chip to Decipher the Influence of Mechanical Forces on the Physiological Cellular Ecosystem.

Moencopi Bernheim-Dennery, Lauriane Gérémie, Julie Brun, Lucas Chassatte, Giacomo Gropplero, Réda Bouras, Jieun Choo, Bertrand Cinquin, Alba Marcellan, Danijela Matic Vignjevic 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
–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

11 authors.

Moencopi Bernheim-DenneryUMR 168, CNRS-Institut Curie, IPGG, PSL Research University, Paris, France.
Lauriane GérémieUMR 168, CNRS-Institut Curie, IPGG, PSL Research University, Paris, France.
Julie BrunUMR 7615, UPMC, Sorbonne-Université, CNRS, ESPCI Paris, PSL Research University, Paris, France.
Lucas ChassatteUMR 168, CNRS-Institut Curie, IPGG, PSL Research University, Paris, France.
Giacomo GroppleroUMR 168, CNRS-Institut Curie, IPGG, PSL Research University, Paris, France.
Réda BourasUMR 144, CNRS-Institut Curie, PSL Research University, Paris, France.
Jieun ChooUMR 144, CNRS-Institut Curie, PSL Research University, Paris, France.
Bertrand CinquinUMR 168, CNRS-Institut Curie, IPGG, PSL Research University, Paris, France.
Alba MarcellanUMR 7615, UPMC, Sorbonne-Université, CNRS, ESPCI Paris, PSL Research University, Paris, France.
Danijela Matic VignjevicUMR 144, CNRS-Institut Curie, PSL Research University, Paris, France.ORCID https://orcid.org/0000-0003-4250-703X
Stéphanie DescroixUMR 168, CNRS-Institut Curie, IPGG, PSL Research University, Paris, France.ORCID https://orcid.org/0000-0003-0027-352X

Funding

European Research Council 772487Institut Pierre-Gilles de Gennes ANR-10-EQPX-34
6 · The paper itself

Abstract

The gut epithelium ensures nutrient absorption and barrier protection, functions tightly linked to its 3D architecture and dynamic mechanical activity. To dissect how mechanical forces influence intestinal physiology, we developed a stretchable 3D colon-on-chip that integrates tunable topography, stiffness and peristalsis-like motion within a physiologically relevant microenvironment. The model employs 3D scaffolds composed of either pure collagen I or mechanically reinforced interpenetrated network (IPN) made of collagen I and PEGDA. Tensile tests mimicking peristalsis revealed that both hydrogels soften upon stretching, with the IPN maintaining higher stiffness than pure collagen. Using this platform, we applied cyclic stretching for 24 to 72 h to co-cultures of stromal and epithelial cells, and systematically assessed the contributions of stiffness, curvature and shear stress. We found that the stretching was a dominant factor governing epithelial behavior, markedly enhancing proliferation and apicobasal polarization without altering differentiation. Altogether, this work introduces a next-generation colon-on-chip that unites mechanical control and biological complexity, providing a powerful tool to unravel how physical cues orchestrate intestinal homeostasis and paving the way for modeling disease states such as colorectal cancer and inflammation.

Indexed as

ColonLab-On-A-Chip DevicesAnimalsCell ProliferationCoculture TechniquesEpithelial CellsHumansHydrogelsIntestinal MucosaMicrophysiological SystemsStress, MechanicalTissue ScaffoldsHydrogelscollagencolon‐on‐chipfibroblastsorganoidsPEGDAperistalsis

Identifiers

PMID41580917
PMCPMC13175293

What OpenQuestion holds

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LicenceCC BY
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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.