Evidence map›Paper›PMID 38193168›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2024

Improving morphological and functional properties of enteric neuronal networks in vitro using a novel upside-down culture approach.

Steven Schulte, Dominique Decker, Bharat Nowduri, Manuela Gries, Anne Christmann, Antoine Meyszner, Holger Rabe, Monika Saumer, Karl-Herbert Schäfer

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

9 authors.

Steven SchulteDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.ORCID 0000-0001-6236-1889
Dominique DeckerDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.
Bharat NowduriDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.
Manuela GriesDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.
Anne ChristmannDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.
Antoine MeysznerDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.
Holger RabeDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.
Monika SaumerDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.
Karl-Herbert SchäferDepartment of Informatics and Microsystems Technology, University of Applied Sciences Kaiserslautern, Zweibrücken, Germany.ORCID 0000-0002-4724-813X

Funding

German Federal Ministry of Education and Research 13FH584IX6
6 · The paper itself

Abstract

The enteric nervous system (ENS) comprises millions of neurons and glia embedded in the wall of the gastrointestinal tract. It not only controls important functions of the gut but also interacts with the immune system, gut microbiota, and the gut-brain axis, thereby playing a key role in the health and disease of the whole organism. Any disturbance of this intricate system is mirrored in an alteration of electrical functionality, making electrophysiological methods important tools for investigating ENS-related disorders. Microelectrode arrays (MEAs) provide an appropriate noninvasive approach to recording signals from multiple neurons or whole networks simultaneously. However, studying isolated cells of the ENS can be challenging, considering the limited time that these cells can be kept vital in vitro. Therefore, we developed an alternative approach cultivating cells on glass samples with spacers (fabricated by photolithography methods). The spacers allow the cells to grow upside down in a spatially confined environment while enabling acute consecutive recordings of multiple ENS cultures on the same MEA. Upside-down culture also shows beneficial effects on the growth and behavior of enteric neural cultures. The number of dead cells was significantly decreased, and neural networks showed a higher resemblance to the myenteric plexus ex vivo while producing more stable signals than cultures grown in the conventional way. Overall, our results indicate that the upside-down approach not only allows to investigate the impact of neurological diseases in vitro but could also offer insights into the growth and development of the ENS under conditions much closer to the in vivo environment.

Indexed as

Enteric Nervous SystemNeuronsMyenteric PlexusSubmucous Plexusenteric nervous systemfractal analysismicroelectrode arraysneuronal cell cultureupside down

Identifiers

PMID38193168
PMCPMC11376983

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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.