Abstract

Exosomes are packaged with a variety of cellular cargo including RNA, DNA, lipids and proteins. For several decades now there has been ongoing debate as to what extent exosomes are the garbage bin of the cell or if these entities function as a distributer of cellular cargo which acts in a meaningful mechanistic way on target cells. Are the contents of exosomes unwanted excess cellular produce or are they selective nucleic acid packaged nanoparticles used to communicate in a paracrine fashion? Overexpressed RNAs and fragments of DNA have been shown to collect into exosomes which are jettisoned from cells in response to particular stimuli to maintain homeostasis suggesting exosomes are functional trash bins of the cell. Other studies however have deciphered selective packaging of particular nucleic acids into exosomes. Nucleic acids packaged into exosomes are increasingly reported to exert transcriptional control on recipient cells, supporting the notion that exosomes may provide a role in signaling and intracellular communication. We survey the literature and conclude that exosomes are multifunctional entities, with a plethora of roles that can each be taken advantage to functionally modulate cells. We also note that the potential utility of developing exosomes as a next generation genetic therapy may in future transform cellular therapies. We also depict three models of methodologies which can be adopted by researchers intending to package nucleic acid in exosomes for developing gene and cell therapy.

Highlights

  • Extracellular vesicles are biological materials released by cells, surrounded by a lipid bilayer membrane which lack a functional nucleus and vary in size range from 30 to 10,000 nm [1,2]

  • We review and contrast the small RNA (miRNA, small nucleolar RNA, PIWI interacting RNAs, tRNA, yRNA), circular RNA, long non-coding RNAs (lncRNAs), messenger RNA (mRNA) and DNA composition of exosomes along with their sorting mechanisms providing insights into the various pathways with regards to developing generation gene and cell therapies

  • While the studies to date suggest that exosomes can be used to deliver particular micro RNAs (miRNAs) signatures to target cells, it became apparent that an ability to program particular miRNAs into exosomes would prove an important step in developing exosomes as therapeutics capable of modulating gene expression

Read more

Summary

Introduction

Extracellular vesicles are biological materials released by cells, surrounded by a lipid bilayer membrane which lack a functional nucleus and vary in size range from 30 to 10,000 nm [1,2]. There is a large body of studies implicating exosome bound miRNAs effective in gene modulation which are distinct functions, independent of the excess production of particular miRNAs in the parent cell source. While the studies to date suggest that exosomes can be used to deliver particular miRNA signatures to target cells, it became apparent that an ability to program particular miRNAs into exosomes would prove an important step in developing exosomes as therapeutics capable of modulating gene expression Towards this goal, studies into the natural enrichment of miR-26c into exosomes led to the observation that miR-26c encapsulated exosomes were directed to skeletal muscle cells and heart via a muscle specific peptide [36]. This peculiar study demonstrated that snoRNA packaging into exosomes is not a mere dump of cellular biproducts but rather is capable of affecting distal gene regulation

PIWI Interacting RNA
LncRNA
Circular RNA
11. Available Toolkit for Developing Exosome-Based Therapies
11.2. Cellular Protein Assisted Packaging Model
11.3. Engineered Protein Mediated Packaging Model
Findings
12. Conclusions
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call