Weiskirchen Ralf, Schröder Sarah K, Weiskirchen Sabine, Buhl Eva Miriam, Melnik Bodo
Institute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry (IFMPEGKC), Rheinisch-Westfälische Technische Hochschule (RWTH) University Hospital Aachen, D-52074 Aachen, Germany.
Electron Microscopy Facility, Institute of Pathology, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen University Hospital, D-52074 Aachen, Germany.
Biomedicines. 2023 Oct 6;11(10):2715. doi: 10.3390/biomedicines11102715.
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.
细胞外囊泡,如外泌体,是由几乎每个细胞产生的小尺寸双层细胞外生物囊泡,在多泡体与质膜融合后释放到周围体液中。基于其来源,它们富含多种生物活性成分,包括蛋白质、脂质、核酸、细胞代谢物和许多其他成分。它们可以附着或融合到靶细胞的膜上,或者通过受体细胞的内吞作用被摄取。特别是,最近已证明母乳外泌体是支持婴儿生长、健康和发育的一个基本因素。此外,已显示源自不同细胞类型的外泌体具有再生、免疫调节和抗炎特性,这表明它们是调节多种疾病发病机制的潜在治疗工具。因此,高效的大量和高纯度分离母乳外泌体的方案是建立临床应用的基础。在此,我们提出了一种易于遵循的从牛和人乳中分离外泌体的方案。电子显微镜分析和纳米颗粒跟踪分析表明,该方案能够分离出高度富集的外泌体组分。纯化的外泌体表达典型的外泌体蛋白标志物CD81和ALIX。