RNA was once thought to have an exclusively intracellular localisation, yet recent discoveries have upended this dogma (1). Various populations of RNA have been discovered in the extracellular milieu, collectively termed exRNA. These RNA subtypes include both protein-coding RNA (mRNA), alongside a multitude of non-coding RNAs, namely microRNAs (miRNA), long noncoding RNAs (lncRNAs), circular RNAs (circRNAs), small nucleolar RNA (snoRNAs), small nuclear RNAs (snRNAs), transfer RNA (tRNAs), ribosomal RNAs (rRNAs) and piwiinteracting RNAs (piRNAs) (2). However, the presence of ribonucleases renders the extracellular environment unfavourable for RNA (3). As such, protection against degradation is afforded in two main ways. Firstly, RNA can be bound in ribonucleoprotein complexes, such as that of Argonaute2 and miRNAs (4). Less frequently RNA can be found as part of lipoprotein complexes (5). Secondly, RNAs can be transported by extracellular vesicles (EVs) (6-8).
EVsComprehensive overviews of EV biogenesis and release have been recently published (9-11). However, in brief, EV is an umbrella term encompassing a heterogeneous assortment of vesicular species released from cells (Figure 1). These can be broadly categorised into exosomes and microvesicles (MVs) (10), although some investigators prefer ectosome as an alternative nomenclature for the latter (9,12). The term exosome was originally used to