Native and bioengineered extracellular vesicles for cardiovascular therapeutics

Nat Rev Cardiol. 2020 Nov;17(11):685-697. doi: 10.1038/s41569-020-0389-5. Epub 2020 Jun 1.

Abstract

Extracellular vesicles (EVs) are a heterogeneous group of natural particles that are relevant to the treatment of cardiovascular diseases. These endogenous vesicles have certain properties that allow them to survive in the extracellular space, bypass biological barriers and deliver their biologically active molecular cargo to recipient cells. Moreover, EVs can be bioengineered to increase their stability, bioactivity, presentation to acceptor cells and capacity for on-target binding at both cell-type-specific and tissue-specific levels. Bioengineering of EVs involves the modification of the donor cell before EV isolation or direct modification of the EV properties after isolation. The therapeutic potential of native EVs and bioengineered EVs has been only minimally explored in the context of cardiovascular diseases. Efforts to harness the therapeutic potential of EVs will require innovative approaches and a comprehensive integration of knowledge gathered from decades of research into molecular-compound delivery. In this Review, we outline the endogenous properties of EVs that make them natural delivery agents as well as the features that can be improved by bioengineering. We also discuss the therapeutic applications of native and bioengineered EVs to cardiovascular diseases and examine the opportunities and challenges that need to be addressed to advance this research area, with an emphasis on clinical translation.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Bioengineering*
  • Brain / physiology
  • Cardiovascular Diseases / therapy*
  • Cell Survival
  • Extracellular Vesicles / metabolism
  • Extracellular Vesicles / transplantation*
  • Extremities / blood supply
  • Heart / physiology
  • Humans
  • Ischemia / therapy*
  • MicroRNAs / metabolism
  • MicroRNAs / therapeutic use
  • Myocardial Infarction / therapy*
  • Myocytes, Cardiac
  • Paracrine Communication
  • Regeneration*
  • Stem Cells / metabolism*
  • Stroke / therapy*

Substances

  • MicroRNAs