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重新评估外泌体组成。

Reassessment of Exosome Composition.

机构信息

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.

出版信息

Cell. 2019 Apr 4;177(2):428-445.e18. doi: 10.1016/j.cell.2019.02.029.

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.

摘要

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。

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Reassessment of Exosome Composition.重新评估外泌体组成。
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