Evidence map›Paper›PMID 40316543›Full record

ArticleNature communications2025

Biomimetic culture substrates for modelling homeostatic intestinal epithelium in vitro.

Sorosh Abdollahi, Bahareh Zarin, Maryam Vatani, Fereshteh Vajhadin, Mohsen Hassani, Pezhman Jalali, Keekyoung Kim, Amir Sanati-Nezhad

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Highly robustFood chemistry: X · 2026
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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

8 authors.

Sorosh AbdollahiDepartment of Biomedical Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.ORCID http://orcid.org/0009-0006-3566-8782
Bahareh ZarinDepartment of Biomedical Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.
Maryam VataniDepartment of Biomedical Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.
Fereshteh VajhadinDepartment of Biomedical Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.
Mohsen HassaniDepartment of Mechanical & Manufacturing Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.ORCID http://orcid.org/0000-0002-6126-0362
Pezhman JalaliDepartment of Biomedical Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.
Keekyoung KimDepartment of Biomedical Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.ORCID http://orcid.org/0000-0002-7442-7117
Amir Sanati-NezhadDepartment of Biomedical Engineering, University of Calgary, Calgary, Alberta, T2N 1N4, Canada. amir.sanatinezhad@ucalgary.ca.ORCID http://orcid.org/0000-0002-2309-2388

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing interest in utilizing three-dimensional (3D) in vitro models with innovative biomaterials to engineer functional tissues arises from the limitations of conventional cell culture methods in accurately reproducing the complex physiological conditions of living organisms. This study presents a strategy for replicating the intricate microenvironment of the intestine by cultivating intestinal cells within bioinspired 3D interfaces that recapitulate the villus-crypt architecture and 3D tissue arrangement of the intestine. Intestinal cells cultured on these biomimetic substrates exhibited phenotypes and differentiation characteristics resembling intestinal-specific cell types, effectively replicating intestinal tissue. Notably, tissue proliferation and differentiation were achieved within 72-120 h-significantly faster than the several weeks required by conventional bioengineered materials, which often pose risks of tissue necrosis or cross-contamination. Additionally, the differentiated cells on these villi-crypts mimicking bio-interfaces exhibit higher production of natural antimicrobial peptides, resulting in reduced pathogenic infection compared to control samples. Furthermore, our method stands out for simplicity in fabrication, eliminating the need for cleanroom procedures and complex microfabrication techniques.

Indexed as

Biomimetic MaterialsBiomimeticsCell Culture TechniquesIntestinal MucosaAnimalsCaco-2 CellsCell Culture Techniques, Three DimensionalCell DifferentiationCell ProliferationHomeostasisHumansMiceModels, BiologicalTissue Engineering

Identifiers

PMID40316543
PMCPMC12048609

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.