Evidence map›Paper›PMID 40483498›Full record

ArticleStem cell research & therapy2025

Unveiling the potential of MSC extracellular vesicles: MiR-122-5p enhancing chondrocyte regeneration in osteoarthritis via autophagy mechanism.

Haifeng Zhang, Yanmeng Yang, Yingnan Wu, Vinitha Denslin, Yi Wei Justin Koh, Ling Liu, Wenhai Zhuo, Wing Moon Raymond Lam, Yinxian Yu, James Hoi Po Hui and 1 more

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

11 authors.

Haifeng Zhang *Department of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Yanmeng Yang *Critical Analytics for Manufacturing Personalised-Medicine, Singapore-MIT Alliance for Research and Technology, Singapore, Singapore.
Yingnan WuDepartment of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Vinitha DenslinNUS Tissue Engineering Program, Life Sciences Institute, National University of Singapore, 27 Medical Drive, DSO (Kent Ridge) Building, level 4, Singapore, 117510, Singapore.
Yi Wei Justin KohDepartment of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Ling LiuResearch Office, Sengkang General Hospital, Singapore, Singapore.
Wenhai ZhuoDepartment of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Wing Moon Raymond LamDepartment of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Yinxian YuDepartment of Orthopaedic Surgery, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200080, China. eastpool@sjtu.edu.cn.
James Hoi Po HuiDepartment of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Zheng YangDepartment of Orthopedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore. dosyz@nus.edu.sg.ORCID http://orcid.org/0000-0003-4275-0590

Funding

Medical-Engineering Cross Project of Shanghai Jiao Tong University YG2022QN076National Medical Research Council of Singapore MOH-000371-00Natural Science Foundation of Shanghai Municipality 23ZR1451700
6 · The paper itself

Abstract

backgroundOsteoarthritis (OA) is one of the most prevalent degenerative joint diseases, while the mechanism by which extracellular vesicles (EVs) promote chondrocyte regeneration remains unclear. The study assessed the effect of hypoxic mesenchymal stem cells (MSCs)-derived EVs on cartilage repair in a rat OA model.

methodsThe effects of EVs on chondrocyte regeneration and autophagy were evaluated in vitro. The influence of specific micro RNA (miRNA) and downstream target genes was examined following EV miRNA sequencing and multiple intersecting database analysis.

resultsWe found EVs derived from hypoxia preconditioned human MSCs to promote cartilage repair in rat OA and enhance the proliferation and migration of chondrocytes in vitro, mediated via chondrocyte autophagy. MiRNA sequencing revealed a significant enrichment of miRNA122-5p in hypoxic MSCs EV, which through regulation of the target gene, DUSP2, mediated autophagy and participated in chondrocyte regeneration. DUSP2 regulation of chondrocyte autophagy could act via the phosphorylation of ERK1/2 and P38.

conclusionsThis study demonstrates that EVs released by MSCs under hypoxic conditions have a beneficial effect on chondrocyte regeneration. A novel mechanism for chondrocyte autophagy is mediated by miR122-5P and DUSP2 target molecules, providing new insights into OA treatments.

Indexed as

AutophagyChondrocytesExtracellular VesiclesMesenchymal Stem CellsMicroRNAsOsteoarthritisRegenerationAnimalsCell ProliferationHumansMaleRatsRats, Sprague-DawleyMicroRNAsMIRN122 microRNA, ratAutophagyChondrocyteDUSP2Extracellular vesiclesmiR-122-5pOsteoarthritis

Identifiers

PMID40483498
PMCPMC12145651

What Socratic holds

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LicenceCC BY-NC-ND
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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.