Evidence map›Paper›PMID 35422485›Full record

ArticleCell death discovery2022

Mesenchymal stem cell-derived exosomal microRNA-182-5p alleviates myocardial ischemia/reperfusion injury by targeting GSDMD in mice.

Rongchuan Yue, Shengzhong Lu, Yu Luo, Jing Zeng, Hao Liang, Dan Qin, Xiaobo Wang, Tao Wang, Jun Pu, Houxiang Hu

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% of its field
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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

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  11. Peripheral nerve repair: innovations and future directions.Journal of translational medicine · 2026
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4 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 1 country.

Rongchuan Yue *Department of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Shengzhong Lu *Department of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Yu Luo *CSCSD, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Jing ZengDepartment of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Hao LiangDepartment of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Dan QinDepartment of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Xiaobo WangDepartment of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Tao WangDepartment of Respiratory and Critical Care Medicine, University of Chinese Academy of Sciences Shenzhen Hospital, Shenzhen, 518100, P.R. China.
Jun PuDepartment of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China.
Houxiang HuDepartment of Cardiology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, P.R. China. hhxiang17@163.com.ORCID http://orcid.org/0000-0002-4855-7145
Affiliated Hospital of North Sichuan Medical College · CNUniversity of Chinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidence indicates that exosomes derived from mesenchymal stem cells (MSCs) confer protective effects against myocardial ischemia/reperfusion (I/R) injury. Exosomes are carriers of potentially protective endogenous molecules, including microRNAs (miRNAs/miRs). The current study set out to test the effects of transferring miR-182-5p from MSC-derived exosomes into myocardial cells on myocardial I/R injury. First, an I/R mouse model was developed by left anterior descending coronary artery occlusion, and myocardial cells were exposed to hypoxia/reoxygenation (H/R) for in vitro I/R model establishment. Loss- and gain-of-function experiments of miR-182-5p and GSDMD were conducted to explore the effects of miR-182-5p via MSC-derived exosomes on cell pyroptosis and viability. GSDMD was robustly expressed in I/R-injured myocardial tissues and H/R-exposed myocardial cells. GSDMD upregulation promoted H/R-induced myocardial cell pyroptosis and reduced viability, corresponding to increased lactate dehydrogenase release, reactive oxygen species production, and pyroptosis. A luciferase assay demonstrated GSDMD as a target of miR-182-5p. In addition, exosomal miR-182-5p was found to diminish GSDMD-dependent cell pyroptosis and inflammation induced by H/R. Furthermore, MSC-derived exosomes carrying miR-182-5p improved cardiac function and reduced myocardial infarction, accompanied with reduced inflammation and cell pyroptosis in vivo. Taken together, our findings suggest a cardioprotective effect of exosomal miR-182-5p against myocardial I/R injury, shedding light on an attractive therapeutic strategy.

Identifiers

PMID35422485
PMCPMC9010441
OpenAlexW4224085366

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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.