Evidence map›Paper›PMID 40411261›Full record

ArticleBiotechnology and bioengineering2025

Development of the Gut Microbial Immune and Epithelial Cellular System (GutMICS) to Investigate the Immunological Role of Gut Anaerobes.

Seo-Young Kwon, Sung-Hyun Jo, Joonha Park, Ji-Hyeon Park, Ye-Rim Kim, Ji-Hyun Baek, Min-Gyu Kim, Bo-Gyeong Choi, Na Youn Hong, Hee Kyoung Jung and 3 more

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

13 authors.

Seo-Young KwonDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Sung-Hyun JoDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Joonha ParkDepartment of Mechanical Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Ji-Hyeon ParkDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Ye-Rim KimDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Ji-Hyun BaekDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Min-Gyu KimDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Bo-Gyeong ChoiDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Na Youn HongCJ CheilJedang, Seoul, Republic of Korea.
Hee Kyoung JungCJ CheilJedang, Seoul, Republic of Korea.
Hee-Wook RyuDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.
Jessie S JeonDepartment of Mechanical Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Yun-Gon KimDepartment of Chemical Engineering, Soongsil University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-7388-2989

Funding

This study was supported by the National Research Foundation of Korea.
6 · The paper itself

Abstract

The gut microbiota plays an essential role in host health by regulating gut barrier function and immune system homeostasis. However, research into the physiological and immunological functions of the gut microbiota using In Vitro models that mimic the immune environment of the gut remains limited. Herein, we developed the Gut Microbial Immune & Epithelial Cellular System (GutMICS), a device for coculturing anaerobic gut microbes with host cells, including intestinal epithelial and immune cells. Coculturing Akkermansia muciniphila with GutMICS sustained host cell viability and microbial activity for 72 h. In a lipopolysaccharide- and tumor necrosis factor-α (TNF-α)-induced inflammation model, A. muciniphila enhanced the intestinal barrier function, prevented barrier disruption, reduced pro-inflammatory cytokines (interleukin (IL)-6, TNF-α), and increased anti-inflammatory cytokines (IL-10). Additionally, A. muciniphila protected against Salmonella Typhimurium infection by reducing adhesion and invasion, thereby preventing pathogen-induced cell death. This study used GutMICS to characterize the anti-inflammatory properties of A. muciniphila and its ability to inhibit pathogen infection, demonstrating that GutMICS is a valuable tool for assessing the effects of anaerobic gut microbes on host cells. The ability of the system to simulate various inflammatory environments is expected to have broad applications in the study of host-microbe interactions.

Indexed as

Epithelial CellsGastrointestinal MicrobiomeIntestinal MucosaAkkermansiaAnimalsCoculture TechniquesCytokinesHumansMiceSalmonella typhimuriumCytokinesAkkermansia mucinipihlaanaerobic‐aerobic cocultureanti‐inflammatory effectshost–microbe interactionIn Vitro coculture modelmacrophageprobiotics

Identifiers

PMID40411261
PMCPMC12322622

What OpenQuestion holds

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LicenceCC BY-NC
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.