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Updated: Dec 4, 2025

In Vivo Nanovector Delivery of a Heart-specific MicroRNA-sponge
Published on: June 15, 2018
Extracellular Vesicle miRNAs in the Promotion of Cardiac Neovascularisation
Despoina Kesidou1, Paula A da Costa Martins2,3, Leon J de Windt2
1Centre for Cardiovascular Science, The Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, United Kingdom.
Insights
Extracellular vesicles (EVs) carrying microRNAs (miRNAs) show promise for stimulating new blood vessel growth after heart attacks. This review explores using EV-bound miRNAs to improve cardiac function and reduce injury following myocardial infarction (MI).
Area of Science:
- Cardiovascular Research
- Regenerative Medicine
- Molecular Biology
Background:
- Cardiovascular disease (CVD) is a leading global cause of mortality, with atherosclerosis leading to myocardial infarction (MI) and heart failure.
- Despite advancements, chronic heart failure post-MI remains a significant clinical challenge, necessitating strategies to reduce cardiac injury.
- Neovascularization is a key therapeutic goal to improve cardiac function after MI, with cell transplantation showing potential but limited by cell retention.
Purpose of the Study:
- To review the process of neovascularization in the context of cardiovascular disease and myocardial infarction.
- To explore the role of extracellular vesicles (EVs) and their encapsulated microRNAs (miRNAs) in promoting angiogenesis and cardiac repair.
- To critically evaluate current methodologies in cell culture, EV isolation, and administration for therapeutic applications.
Main Methods:
- Literature review focusing on neovascularization, extracellular vesicles (EVs), and microRNAs (miRNAs) in cardiovascular research.
- Analysis of pre-clinical studies investigating cell transplantation and paracrine mechanisms post-myocardial infarction.
- Critical assessment of techniques for cell culture, EV isolation, and delivery strategies for therapeutic interventions.
Main Results:
- Extracellular vesicles (EVs) act as crucial mediators of intercellular communication, transferring bioactive molecules like miRNAs.
- EV-derived miRNAs have demonstrated the capacity to stimulate angiogenesis by influencing endothelial cells (ECs).
- Pre-clinical studies suggest a paracrine mechanism, mediated by factors like EVs, contributes to cardiac function improvement post-MI.
Conclusions:
- EVs and their miRNA cargo represent a promising therapeutic avenue for promoting neovascularization and mitigating cardiac damage post-MI.
- Further research and optimization of EV-based therapeutic strategies, including isolation and administration methods, are warranted.
- Understanding EV-miRNA interactions is key to developing novel treatments for heart failure following myocardial infarction.
Abstract:
Cardiovascular disease (CVD) is the leading cause of mortality worldwide claiming almost 17. 9 million deaths annually. A primary cause is atherosclerosis within the coronary arteries, which restricts blood flow to the heart muscle resulting in myocardial infarction (MI) and cardiac cell death. Despite substantial progress in the management of coronary heart disease (CHD), there is still a significant number of patients developing chronic heart failure post-MI. Recent research has been focused on promoting neovascularisation post-MI with the ultimate goal being to reduce the extent of injury and improve function in the failing myocardium. Cardiac cell transplantation studies in pre-clinical models have shown improvement in cardiac function; nonetheless, poor retention of the cells has indicated a paracrine mechanism for the observed improvement. Cell communication in a paracrine manner is controlled by various mechanisms, including extracellular vesicles (EVs). EVs have emerged as novel regulators of intercellular communication, by transferring molecules able to influence molecular pathways in the recipient cell. Several studies have demonstrated the ability of EVs to stimulate angiogenesis by transferring microRNA (miRNA, miR) molecules to endothelial cells (ECs). In this review, we describe the process of neovascularisation and current developments in modulating neovascularisation in the heart using miRNAs and EV-bound miRNAs. Furthermore, we critically evaluate methods used in cell culture, EV isolation and administration.
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