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.

Frontiers in Physiology
|October 26, 2020
PubMed

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.