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. 2023 May;1523(1):24-37.
doi: 10.1111/nyas.14974. Epub 2023 Mar 18.

Exosomes, microvesicles, and other extracellular vesicles-a Keystone Symposia report

Affiliations

Exosomes, microvesicles, and other extracellular vesicles-a Keystone Symposia report

Jennifer Cable et al. Ann N Y Acad Sci. 2023 May.

Abstract

Extracellular vesicles (EVs) are small, lipid-bilayer-bound particles released by cells that can contain important bioactive molecules, including lipids, RNAs, and proteins. Once released in the extracellular environment, EVs can act as messengers locally as well as to distant tissues to coordinate tissue homeostasis and systemic responses. There is a growing interest in not only understanding the physiology of EVs as signaling particles but also leveraging them as minimally invasive diagnostic and prognostic biomarkers (e.g., they can be found in biofluids) and drug-delivery vehicles. On October 30-November 2, 2022, researchers in the EV field convened for the Keystone symposium "Exosomes, Microvesicles, and Other Extracellular Vesicles" to discuss developing standardized language and methodology, new data on the basic biology of EVs and potential clinical utility, as well as novel technologies to isolate and characterize EVs.

Keywords: exomere; exosome; extracellular RNA; extracellular vesicle; mitovesicle; supermere.

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Conflict of interest statement

COMPETING INTERESTS

Niek Dekker is employed by AstraZeneca R&D. Michele de Palma is an inventor on a patent application filed by EPFL (WO2017134100A1) on engineered dendritic cell vaccines and serves on the scientific advisory board of EVIR Therapeutics, a start-up focused on the development of engineered dendritic cell vaccines for cancer therapy.

Figures

FIGURE 1
FIGURE 1
EV Fingerprinting, a new methodology that uses multiparametric flow cytometry data to capture the heterogeneity of EV populations.
FIGURE 2
FIGURE 2
EV Painting: cell surface labeling via EVs. Cells of choice (in the depicted example, tumor cells) are engineered to express the CD63-GFP fusion protein (A) or a membrane-bound form of Sortase-A (B) and its fluorescent substrate (as secreted protein). In vitro flow cytometric analyses of the cells are shown. The secreted fluorescent substrate can be observed in the tumor stroma in vivo (A, right), suggesting that the Sortase-A substrate is released from tumor cells and it drains into sentinel lymph nodes (not shown). In tumor-draining lymph nodes (B, right), 3D imaging reconstructions show CD169+ sub-capsular sinus macrophages are extensively labeled by EVs, as expected. Migratory and resident XCR1+ dendritic cells are mostly lacking EV binding, possibly as a result of internalization and degradation of EV-bound antigens for cross-presentation. Of note, several small, round, lymphoid-like cells have been EV painted. Scale bar: 50 um. Each image is a projection of 15um-deep volumes taken at the indicated depths. [Correction added on 23 March 2023, after first online publication: Legend for Figure 2 was updated.]
FIGURE 3
FIGURE 3
CryoEM of a mitovesicle.

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