Evidence map›Paper›PMID 36696015›Full record

ArticleStem cell reviews and reports2023

Extracellular Vesicles from NMN Preconditioned Mesenchymal Stem Cells Ameliorated Myocardial Infarction via miR-210-3p Promoted Angiogenesis.

Yanan Pu, Chunyu Li, Xin Qi, Rui Xu, Liyang Dong, Yi Jiang, Qingyun Gong, Di Wang, Rong Cheng, Cheng Zhang and 1 more

Abstract read
In one paragraph

Article in Stem cell reviews and reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  9. Article
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  11. Extracellular vesicle therapeutics for cardiac repair.Journal of molecular and cellular cardiology · 2025
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  13. Article
  14. Review
  15. Review
  16. Review
  17. The Potential of Mesenchymal Stem Cell-Derived Exosomes in Cardiac Repair.International journal of molecular sciences · 2024
    Review
  18. Review
  19. Article
  20. 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

11 authors.

Yanan PuOutpatient & Emergency Management Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.ORCID 0000-0002-3833-8934
Chunyu LiWomen & Children Intensive Care Unit, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Xin QiState Key Lab of Reproductive Medicine, Jiangsu Key Laboratory of Pathogen Biology, Department of Pathogen Biology and Immunology, Center for Global Health, Nanjing Medical University, Nanjing, 211166, Jiangsu, China.
Rui XuOutpatient & Emergency Management Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Liyang DongDepartment of Nuclear Medicine, The Affiliated Hospital of Jiangsu University, Zhenjiang, 212000, Jiangsu, China.
Yi JiangOutpatient & Emergency Management Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Qingyun GongOutpatient & Emergency Management Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Di WangOutpatient & Emergency Management Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Rong ChengOutpatient & Emergency Management Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Cheng ZhangWomen & Children Central Laboratory, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China. czhang@njmu.edu.cn.
Yan ChenOutpatient & Emergency Management Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China. chenyandoc@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cell-derived extracellular vesicles (MSCs-EVs) possess cardioprotection in acute myocardial infarction. Nevertheless, the therapeutic intervention potential and the molecular mechanism of EVs from NMN (Nicotinamide mononucleotide) preconditioned hUCMSCs (N-EVs) in acute myocardial infarction remains unknown. In the present study, EVs from hUCMSCs (M-EVs) and N-EVs were identified by electron microscopy, immunoblotting and nanoparticle tracking analysis. Compared with M-EVs, N-EVs significantly increased the proliferation, migration, and angiogenesis of HUVECs. Meanwhile, N-EVs markedly reduced apoptosis and cardiac fibrosis and promoted angiogenesis in the peri-infarct region in the MI rats. A high-throughput miRNA sequencing and qPCR methods analysis revealed that miR-210-3p was abundant in N-EVs and the expression of miR-210-3p was obviously upregulated in HUVECs after N-EVs treated. Overexpression of miR-210-3p in HUVECs significantly enhanced the tube formation, migration and proliferative capacities of HUVECs. However, downregulation of miR-210-3p in HUVECs markedly decreased the tube formation, migration and proliferative capacities of HUVECs. Furthermore, bioinformatics analysis and luciferase assays revealed that EphrinA3 (EFNA3) was a direct target of miR-210-3p. Knockdown of miR-210-3p in N-EVs significantly impaired its ability to protect the heart after myocardial infarction. Altogether, these results indicated that N-EVs promoted the infarct healing through improvement of angiogenesis by miR-210-3p via targeting the EFNA3. Created with Biorender.com.

Indexed as

Extracellular VesiclesMesenchymal Stem CellsMicroRNAsMyocardial InfarctionAnimalsHeartRatsMicroRNAsMIRN210 microRNA, ratAngiogenesisEVsMesenchymal stem cellsmiR-210-3pNMN

Identifiers

PMID36696015
PMCPMC10185590

What Socratic holds

Textmetadata
LicenceCC BY
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.