Evidence map›Paper›PMID 42765439›Full record

ArticleImmunity, inflammation and disease2026

Mesenchymal Stem Cells Alleviate Crohn's Disease by Regulating CBS-Mediated Ferroptosis.

Zhixi Huang, Xiaofang Xu, Zhou Huang, Bing Han, Dan Jiang, Xiaodan Lv, Ziqian Huang, Guangfu Lin, Fengxiang Huang, Yu Li and 4 more

Abstract read
In one paragraph

Article in Immunity, inflammation and disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

14 authors.

Zhixi HuangDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Xiaofang XuDepartment of Gastroenterology, Guangxi Hospital Division of The First Affiliated Hospital of Sun Yat-sen University, Nanning, China.ORCID https://orcid.org/0000-0001-7986-1740
Zhou HuangDepartment of Emergency, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Bing HanDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID https://orcid.org/0000-0001-7600-6693
Dan JiangDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Xiaodan LvDepartment of Clinical Experimental Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Ziqian HuangDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID https://orcid.org/0009-0009-7340-4480
Guangfu LinDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Fengxiang HuangDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yu LiDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Lichun HanDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID https://orcid.org/0000-0003-2793-5693
Deyi ChenDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Jianing LinDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Xiaoping LvDepartment of Gastroenterology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.ORCID https://orcid.org/0000-0002-6319-467X

Funding

The Development and Application of Medical and Health Appropriate Technology Project in Guangxi Zhuang Autonomous Region S2018049The Guangxi Zhuang Autonomous Region Health Commission of Scientific Research Project Z-A20250164The Innovation Project of Guangxi Graduate Education YCBZ2022079The Joint Project on Regional High-Incidence Diseases Research of the Guangxi Natural Science Foundation 2023GXNSFDA026024The National Natural Science Foundation of China 81860104The Self-financing Project of the Health Commission of Guangxi Zhuang Autonomous Region Z20200398The Self-financing Project of the Health Commission of Guangxi Zhuang Autonomous Region Z-A20230474The Youth Science Foundation of Guangxi Medical University GXMUYSF202316
6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) possess immunoregulatory properties and have been shown to alleviate symptoms of Crohn's disease (CD). While ferroptosis has been implicated in the onset of CD, the precise connection between MSCs, CD, and ferroptosis remains unclear. This study sought to explore whether MSCs could alleviate CD by inhibiting ferroptosis. MATERIALS AND

methodsWe screened the hub genes involved in both ferroptosis and CD and validated them in clinical colon biopsies by immunohistochemistry (IHC). MSCs were administered intraperitoneally to mice with colitis induced by trinitrobenzene sulfonic acid (TNBS) enema to evaluate the therapeutic effect. Additionally, a rescue experiment was conducted by co-treating colitis mice with a cystathionine-β-synthase (CBS) inhibitor (aminooxyacetic acid, AOAA) and MSCs to further explore the mechanism of the MSCs-CBS-ferroptosis axis. The expression levels of CBS and ferroptosis-related markers in colonic tissues were assessed by real-time quantitative polymerase chain reaction (RT-qPCR), western blot, and IHC.

resultsBioinformatics and machine learning identified CBS as a hub gene in both CD and ferroptosis. IHC revealed that CBS expression was downregulated in colon tissues from CD patients. MSCs treatment significantly reduced pathological symptoms and intestinal inflammation in colitis mice. MSCs increased CBS expression, which had been diminished in colitis mice. Additionally, MSCs increased glutathione (GSH) and glutathione peroxidase 4 (GPX4) expression, thereby inhibiting ferroptosis activation. In a rescue experiment, co-treatment with AOAA and MSCs exacerbated intestinal inflammation and reversed the elevation of CBS and ferroptosis-related markers. DISCUSSION: This study demonstrates that MSCs alleviate the symptoms of CD by regulating CBS-mediated ferroptosis.

Indexed as

Crohn DiseaseCystathionine beta-SynthaseFerroptosisMesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsColitisColonDisease Models, AnimalFemaleHumansMaleMiceTrinitrobenzenesulfonic AcidCystathionine beta-SynthaseTrinitrobenzenesulfonic AcidCBSCrohn's diseaseferroptosismesenchymal stem cells

Identifiers

PMID42765439
PMCPMC13591549

What Socratic holds

Textmetadata
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 Socratic graph.