fig2

Extracellular vesicles: cross-organismal RNA trafficking in plants, microbes, and mammalian cells

Figure 2. Heterogeneous populations of EVs isolated from plants. There are at least four known EV populations that have been isolated from plants: TET-positive EVs, PEN1-positive EVs, autophagy-related EVs, and pollenosomes. They have different sizes, densities, cargoes, and intracellular origins. Pathogen infection induces secretion of both TET-positive EVs and PEN1-positive EVs[56]. In the process of EV isolation, final centrifugation of 40,000 × g (P40) pellets larger and heavier vesicles such as PEN1-positive EVs and large EVs, non-vesicular free RNA, and RNA-protein complexes[30,79]. Small EVs, such as TET-positive EVs, are mainly present in the supernatant after 40,000 × g centrifugation and require a higher speed of ultracentrifugation at 100,000 × g for collection (P100)[30,56]. Autophagy-related EVs marked with ATG8a were collected using 100,000 × g from plants during the autophagy process within cells[64]. Pollenosomes secreted during pollen germination and pollen tube growth were collected at 100,000 × g from in-vitro pollen gemination media[59]. EXPO-derived EVs originate from the plant-specific organelle EXPO, are marked by the protein Exo70E2, and have not yet been isolated from plants[71]. This figure was created with https://www.biorender.com/.

Extracellular Vesicles and Circulating Nucleic Acids
ISSN 2767-6641 (Online)
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