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Reassessment of Exosome Composition
Author(s) -
Dennis K. Jeppesen,
Aidan M. Fenix,
Jeffrey L. Franklin,
James N. Higginbotham,
Qin Zhang,
Lisa J. Zimmerman,
D.C. Liebler,
Jie Ping,
Qi Liu,
Rachel Evans,
William H. Fissell,
James G. Patton,
Leonard H. Rome,
Dylan T. Burnette,
Robert J. Coffey
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.02.029
Subject(s) - microvesicles , biology , exosome , extracellular vesicle , microbiology and biotechnology , extracellular , annexin a2 , rna , endosome , vesicle , biochemistry , annexin , microrna , intracellular , cell , gene , membrane
The heterogeneity of small extracellular vesicles and presence of non-vesicular extracellular matter have led to debate about contents and functional properties of exosomes. Here, we employ high-resolution density gradient fractionation and direct immunoaffinity capture to precisely characterize the RNA, DNA, and protein constituents of exosomes and other non-vesicle material. Extracellular RNA, RNA-binding proteins, and other cellular proteins are differentially expressed in exosomes and non-vesicle compartments. Argonaute 1-4, glycolytic enzymes, and cytoskeletal proteins were not detected in exosomes. We identify annexin A1 as a specific marker for microvesicles that are shed directly from the plasma membrane. We further show that small extracellular vesicles are not vehicles of active DNA release. Instead, we propose a new model for active secretion of extracellular DNA through an autophagy- and multivesicular-endosome-dependent but exosome-independent mechanism. This study demonstrates the need for a reassessment of exosome composition and offers a framework for a clearer understanding of extracellular vesicle heterogeneity.

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