KOR

e-Article

Reassessment of Exosome Composition
Document Type
article
Source
Cell. 177(2)
Subject
Biochemistry and Cell Biology
Biological Sciences
Genetics
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
Annexin A1
Argonaute Proteins
Cell Line
Tumor
Cell Membrane
Cell-Derived Microparticles
DNA
Exosomes
Extracellular Vesicles
Female
Humans
Lysosomes
Male
Proteins
RNA
Argonaute
amphisomes
annexin
autophagy
exomeres
exosomes
extracellular DNA
extracellular RNA
extracellular vesicles
microvesicles
Medical and Health Sciences
Developmental Biology
Biological sciences
Biomedical and clinical sciences
Language
Abstract
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.