Evidence map›Paper›PMID 40691615›Full record

ArticleStem cell research & therapy2025

CD317 stabilizes TNFR1 and confers the anti-inflammatory functions of MSCs via NF-κB/TSG6 pathway.

Si Chen, Lan Yao, Xin Wen, Xianqi Wang, Lin Chen, Jingting Zhang, Jianyong Xu

Abstract read
In one paragraph

Article in Stem cell research & therapy, 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

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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

7 authors.

Si ChenDepartment of Immunology, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518060, People's Republic of China.
Lan YaoShenzhen Key Laboratory of Reproductive Immunology for Peri-Implantation, Shenzhen Zhongshan Institute for Reproductive Medicine and Genetics, Shenzhen Zhongshan Obstetrics & Gynecology Hospital, Shenzhen, 518000, People's Republic of China.
Xin WenSchool of Pharmaceutical Sciences, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518060, People's Republic of China.
Xianqi WangDepartment of Immunology, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518060, People's Republic of China.
Lin ChenDepartment of Immunology, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518060, People's Republic of China.
Jingting ZhangShenzhen Key Laboratory of Reproductive Immunology for Peri-Implantation, Shenzhen Zhongshan Institute for Reproductive Medicine and Genetics, Shenzhen Zhongshan Obstetrics & Gynecology Hospital, Shenzhen, 518000, People's Republic of China.
Jianyong XuShenzhen Key Laboratory of Reproductive Immunology for Peri-Implantation, Shenzhen Zhongshan Institute for Reproductive Medicine and Genetics, Shenzhen Zhongshan Obstetrics & Gynecology Hospital, Shenzhen, 518000, People's Republic of China. xujianyong820915@163.com.ORCID http://orcid.org/0000-0003-1910-4603

Funding

Basic and Applied Basic Research Foundation of Guangdong Province Applied Basic Research FoundationBasic and Applied Basic Research Foundation of Guangdong Province Guangdong BasicFundamental Research Project of the Shenzhen Science and Technology Innovation Commission 20231120113324002
6 · The paper itself

Abstract

backgroundAlthough both pre-clinical and clinical studies show promising outcomes, resulting in rapid growth of clinical trials of MSC-based therapies in recent years, the heterogeneity and therapeutic inconsistency of MSCs have severely hampered their clinical applications. Purifying homogenous MSC populations with enhanced specific functions represents one promising approach. We have demonstrated recently that the CD317

methodsIn the current study, we performed both in vitro and in vivo investigations to delineate whether and how CD317 regulates the immune modulation function of MSCs.

resultsOur data here indicate that the CD317 directly contributes to the immune suppression function of MSCs stimulated by TNF-α through up-regulating TSG6 via CD317/lipid-raft/TNFR1 complex. The CD317 stabilizes the TNFR1 complex, resulting in hyper-activation of the NF-κB pathway and up-regulation of TSG6, which confers the therapeutic effects of MSCs on the mouse model of ALI (acute lung injury) and IBD (inflammatory bowel disease).

conclusionsThus, the CD317 stabilizes TNFR1 and confers the anti-inflammatory functions of MSCs via NF-κB/TSG6 Pathway.

Indexed as

Antigens, CDCell Adhesion MoleculesMesenchymal Stem CellsNF-kappa BReceptors, Tumor Necrosis Factor, Type IAcute Lung InjuryAnimalsDisease Models, AnimalHumansMaleMesenchymal Stem Cell TransplantationMiceMice, Inbred C57BLSignal TransductionTumor Necrosis Factor-alphaAntigens, CDCell Adhesion MoleculesNF-kappa BReceptors, Tumor Necrosis Factor, Type ITnfaip6 protein, mouseTumor Necrosis Factor-alphaCD317ImmunosuppressionMesenchymal stem/stromal cellsMSCsTSG6

Identifiers

PMID40691615
PMCPMC12282008

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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.