Evidence map›Paper›PMID 41292982›Full record

ArticlebioRxiv : the preprint server for biology2025

Physical, chemical, and structural properties of human gastric organoid-derived mucus.

Katrina N Lyon, Barkan Sidar, Cameron Dudiak, Chloe Vermulm, Grace Jordan, Thomas A Sebrell, Alexis Burcham, Luke Domanico, Richard F Helm, Wentian Liao and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

16 authors.

Katrina N LyonDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, MT.
Barkan SidarChemical and Biological Engineering Department, Montana State University, Bozeman, MT.
Cameron DudiakCenter for Biofilm Engineering.
Chloe VermulmChemical and Biological Engineering Department, Montana State University, Bozeman, MT.
Grace JordanDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, MT.
Thomas A SebrellDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, MT.
Alexis BurchamDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, MT.
Luke DomanicoDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, MT.
Richard F HelmDepartment of Biochemistry, Virginia Tech, Blacksburg, VA.
Wentian LiaoDepartment of Physics, Boston University, Boston, MA.
Bret DavisDepartment of Physics, Montana State University, Bozeman, MT.
Jennifer BrownChemical and Biological Engineering Department, Montana State University, Bozeman, MT.
Scott G McCallaChemical and Biological Engineering Department, Montana State University, Bozeman, MT.
James N WilkingChemical and Biological Engineering Department, Montana State University, Bozeman, MT.
Rama BansilDepartment of Physics, Boston University, Boston, MA.
Diane BimczokDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, MT.ORCID 0000-0002-8817-7243

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Using the GoFlowChip to understand SARS-CoV-2 infection of the gastrointestinal mucosa of humans and batsU01EB029242 · NIBIB · MONTANA STATE UNIVERSITY - BOZEMAN · PI BIMCZOK, DIANE, WALK, SETH T · 2019 to 2023
$4.0M
Modeling gastric mucus layer physiologyR01GM131408 · NIGMS · UNIVERSITY OF UTAH · PI FOGELSON, AARON L · 2018 to 2021
$1.5M
NCATS NIH HHS UL1 TR002319NIBIB NIH HHS U01 EB029242NIGMS NIH HHS R01 GM131408
6 · The paper itself

Abstract

The gastric mucus layer protects the epithelium from gastric acid and ingested pathogens. However, studies of human gastric mucus have been limited due to poor accessibility of native human mucus and the abundance of contaminants in these samples. Here, we explored the potential of human gastric organoids as models for mucus production. Immunofluorescence staining confirmed that the organoids produced mucus containing MUC5AC and MUC6. The luminal mucus had viscoelastic properties similar to those of native human gastric mucus, as determined by particle tracking microrheology. To collect organoid-produced gastric mucus, termed bioengineered gastric mucus (BGM), organoids were cultured as monolayers at the air-liquid interface (ALI), and apically-secreted mucus was harvested and analyzed by MUC5AC ELISA, proteomics, CryoFE-SEM, and bulk rheometry. BGM contained high-molecular weight molecules also found in native gastric mucus, including MUC5AC. Proteomic analysis confirmed that BGM contained MUC5AC, MUC6, MUC1, and other stomach-specific molecules such as gastricsin, olfactomedin 4, and gastrokine. CryoFE-SEM showed that both BGM and native mucus had a porous structure and a characteristic honeycomb scaffold. Bulk rheometry confirmed that BGM exhibited shear thinning and predominantly elastic behavior, consistent with native mucus. Collectively, these findings indicate that BGM is an accessible alternative to native gastric mucus that can be produced on-demand for

Indexed as

air-liquid interfacegastric epithelial barriergastric mucus layermicrorheologyorganoid lumenorganoids

Identifiers

PMID41292982
PMCPMC12642607

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.