Cardioprotective microRNAs (protectomiRs) in a pig model of acute myocardial infarction and cardioprotection by ischaemic conditioning: MiR-450a
- PMID: 39294819
- DOI: 10.1111/bph.17313
Cardioprotective microRNAs (protectomiRs) in a pig model of acute myocardial infarction and cardioprotection by ischaemic conditioning: MiR-450a
Abstract
Background and purpose: Cardioprotective miRNAs (protectomiRs) are promising therapeutic tools. Here, we aimed to identify protectomiRs in a translational porcine model of acute myocardial infarction (AMI) and to validate their cardiocytoprotective effect.
Experimental approach: ProtectomiR candidates were selected after systematic analysis of miRNA expression changes in cardiac tissue samples from a closed-chest AMI model in pigs subjected to sham operation, AMI and ischaemic preconditioning, postconditioning or remote preconditioning, respectively. Cross-species orthologue protectomiR candidates were validated in simulated ischaemia-reperfusion injury (sI/R) model of isolated rat ocardiomyocytes and in human AC16 cells as well. For miR-450a, we performed target prediction and analysed the potential mechanisms of action by GO enrichment and KEGG pathway analysis.
Key results: Out of the 220 detected miRNAs, four were up-regulated and 10 were down-regulated due to all three conditionings versus AMI. MiR-450a and miR-451 mimics at 25 nM were protective in rat cardiomyocytes, and miR-450a showed protection in human cardiomyocytes as well. MiR-450a has 3987 predicted mRNA targets in pigs, 4279 in rats and 8328 in humans. Of these, 607 genes are expressed in all three species. A total of 421 common enriched GO terms were identified in all three species, whereas KEGG pathway analysis revealed 13 common pathways.
Conclusion and implications: This is the first demonstration that miR-450a is associated with cardioprotection by ischaemic conditioning in a clinically relevant porcine model and shows cardiocytoprotective effect in human cardiomyocytes, making it a promising drug candidate. The mechanism of action of miR-450a involves multiple cardioprotective pathways.
Linked articles: This article is part of a themed issue Non-coding RNA Therapeutics. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v182.2/issuetoc.
Keywords: miR‐450a; miR‐451; microRNA; pig; postconditioning; preconditioning; protectomiR; remote conditioning.
© 2024 The Author(s). British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.
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Grants and funding
- OTKA ANN 107803/Hungarian Scientific Research Fund
- OTKA K-105555/Hungarian Scientific Research Fund
- 2018-1.3.1-VKE-2018-00024/National Research, Development and Innovation Office
- NVKP-16-1-2016-0017 National Heart Program/National Research, Development and Innovation Office
- OTKA-FK 134751/National Research, Development and Innovation Office
- TKP/ITM/NFKIH/National Research, Development and Innovation Office
- OTKAK21-139105/National Research, Development and Innovation Office
- RRF-2.3.1-21-2022-00003/European Union
- EU COST Action CardioRNA.eu, Cardioprotection.eu
- 88öu1/Austrian-Hungarian Action Scholarship
- 739593/European Union's Horizon 2020
- 2019-1.1.1-PIACI-KFI-2019-00367/National Research, Development and Innovation Fund
- 2020-1.1.5-GYORSÍTÓSÁV-2021-00011/National Research, Development and Innovation Fund
- ÚNKP-20-5/National Research, Development and Innovation Fund
- ÚNKP-23-4-II-SE-34/National Research, Development and Innovation Fund
- János Bolyai Research Scholarship of Hungarian Academy of Sciences
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