Evidence map›Paper›PMID 42716962›Full record

ArticleScientific reports2026

Optimized air-liquid interface cultivation enhances survival and integrity of mouse colon precision-cut tissue slices.

Daniela Thalheim, Jessica Knittel, Katharina Erlenbach-Wuensch, Roland Nagy, Rainer Tietze, Arndt Hartmann, Regine Schneider-Stock

Abstract read
In one paragraph

Article in Scientific reports, 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

7 authors.

Daniela ThalheimInstitute of Pathology, Experimental Tumorpathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstrasse 22, 91054, Erlangen, Germany.
Jessica KnittelInstitute of Pathology, Experimental Tumorpathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstrasse 22, 91054, Erlangen, Germany.
Katharina Erlenbach-WuenschInstitute of Pathology, Experimental Tumorpathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstrasse 22, 91054, Erlangen, Germany.
Roland NagyInstitute of Applied Quantum Technologies (AQuT.), Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Rainer TietzeDepartment of Otorhinolaryngology, Head and Neck Surgery, Section of Experimental Oncology and Nanomedicine (SEON), Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Arndt HartmannInstitute of Pathology, Experimental Tumorpathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstrasse 22, 91054, Erlangen, Germany.
Regine Schneider-StockInstitute of Pathology, Experimental Tumorpathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsstrasse 22, 91054, Erlangen, Germany. regine.schneider-stock@uk-erlangen.de.ORCID 0000-0003-0482-531X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mouse colon precision-cut tissue slices (cPCTS) serve as valuable models for studying physiology, toxicology, and immunology. They retain a three-dimensional structure with physiological cell composition and intact metabolic and immune functions. Additionally, cPCTS support the 3R principle by reducing animal use. This study aimed to optimize cPCTS cultivation to maintain cell integrity, minimize damage, and enhance survival of the multilayer intestinal structure. We established an air-liquid interface (ALI) cultivation system, where cPCTS rest on a semi-permeable insert membrane with medium beneath and direct air exposure above. We compared the effects of different oxygen concentrations on cPCTS survival using LDH assays, TUNEL staining, qPCR, and immunohistochemistry. cPCTS preserved the characteristic colonic architecture for up to 120 h, with optimal tissue integrity maintained for at least 96 h. Compared with 80% O

Indexed as

ColonTissue Culture TechniquesAirAnimalsApoptosisCell SurvivalDNA DamageIntestinal MucosaMiceOxidative StressOxygenOxygenColonExtracellular matrixHistologyOrganotypic tissue cultureOxygen

Identifiers

PMID42716962
PMCPMC13558742

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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.