微泡
外体
细胞生物学
内吞作用
细胞外
胞外囊泡
细胞
生物
纳米粒子跟踪分析
细胞内
化学
生物化学
小RNA
基因
作者
Ralf Weiskirchen,Sarah K. Schröder,Sabine Weiskirchen,Eva Miriam Buhl,Bodo C. Melnik
出处
期刊:Biomedicines
[MDPI AG]
日期:2023-10-06
卷期号:11 (10): 2715-2715
被引量:5
标识
DOI:10.3390/biomedicines11102715
摘要
Extracellular vesicles such as exosomes are small-sized, bilayered extracellular biovesicles generated by almost every cell and released into the surrounding body fluids upon the fusion of multivesicular bodies and the plasma membrane. Based on their origin, they are enriched with a variety of biologically active components including proteins, lipids, nucleic acids, cellular metabolites, and many other constituents. They can either attach or fuse with the membrane of a target cell, or alternatively be taking up via endocytosis by a recipient cell. In particular, milk exosomes have been recently shown to be a fundamental factor supporting infant growth, health, and development. In addition, exosomes derived from different cell types have been shown to possess regenerative, immunomodulatory, and anti-inflammatory properties, suggesting that they are a potential therapeutic tool in modulating the pathogenesis of diverse diseases. Therefore, efficient protocols for the isolation of milk exosomes in a high quantity and purity are the basis for establishing clinical applications. Here, we present an easy-to-follow protocol for exosome isolation from bovine and human milk. Electron microscopic analysis and nanoparticle tracking analysis reveal that the protocols allow the isolation of highly enriched fractions of exosomes. The purified exosomes express the typical exosomal protein markers, CD81 and ALIX.
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