Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Cell. 2019 Apr 4;177(2):428-445.e18. doi: 10.1016/j.cell.2019.02.029.
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.
小细胞外囊泡的异质性和非囊泡细胞外物质的存在,导致了关于外泌体内容物和功能特性的争论。在这里,我们采用高分辨率密度梯度分离和直接免疫亲和捕获技术,精确地表征外泌体和其他非囊泡物质的 RNA、DNA 和蛋白质成分。细胞外 RNA、RNA 结合蛋白和其他细胞蛋白在外泌体和非囊泡区室中差异表达。外泌体中未检测到 Argonaute 1-4、糖酵解酶和细胞骨架蛋白。我们鉴定出 annexin A1 是直接从质膜脱落的微囊泡的特异性标记物。我们进一步表明,小细胞外囊泡不是主动 DNA 释放的载体。相反,我们提出了一种新的模型,即通过自噬和多泡体依赖但外泌体独立的机制主动分泌细胞外 DNA。本研究表明需要重新评估外泌体的组成,并为更清楚地了解细胞外囊泡的异质性提供了一个框架。