Lässer Cecilia, Eldh Maria, Lötvall Jan
Krefting Research Centre, Department of Internal Medicine, Sahlgrenska Academy, University of Gothenburg.
J Vis Exp. 2012 Jan 9(59):e3037. doi: 10.3791/3037.
The field of exosome research is rapidly expanding, with a dramatic increase in publications in recent years. These small vesicles (30-100 nm) of endocytic origin were first proposed to function as a way for reticulocytes to eradicate the transferrin receptor while maturing into erythrocytes, and were later named exosomes. Exosomes are formed by inward budding of late endosomes, producing multivesicular bodies (MVBs), and are released into the environment by fusion of the MVBs with the plasma membrane. Since the first discovery of exosomes, a wide range of cells have been shown to release these vesicles. Exosomes have also been detected in several biological fluids, including plasma, nasal lavage fluid, saliva and breast milk. Furthermore, it has been demonstrated that the content and function of exosomes depends on the originating cell and the conditions under which they are produced. A variety of functions have been demonstrated for exosomes, such as induction of tolerance against allergen, eradication of established tumors in mice, inhibition and activation of natural killer cells, promotion of differentiation into T regulatory cells, stimulation of T cell proliferation and induction of T cell apoptosis. Year 2007 we demonstrated that exosomes released from mast cells contain messenger RNA (mRNA) and microRNA (miRNA), and that the RNA can be shuttled from one cell to another via exosomes. In the recipient cells, the mRNA shuttled by exosomes was shown to be translated into protein, suggesting a regulatory function of the transferred RNA. Further, we have also shown that exosomes derived from cells grown under oxidative stress can induce tolerance against further stress in recipient cells and thus suggest a biological function of the exosomal shuttle RNA. Cell culture media and biological fluids contain a mixture of vesicles and shed fragments. A high quality isolation method for exosomes, followed by characterization and identification of the exosomes and their content, is therefore crucial to distinguish exosomes from other vesicles and particles. Here, we present a method for the isolation of exosomes from both cell culture medium and body fluids. This isolation method is based on repeated centrifugation and filtration steps, followed by a final ultracentrifugation step in which the exosomes are pelleted. Important methods to identify the exosomes and characterize the exosomal morphology and protein content are highlighted, including electron microscopy, flow cytometry and Western blot. The purification of the total exosomal RNA is based on spin column chromatography and the exosomal RNA yield and size distribution is analyzed using a Bioanalyzer.
外泌体研究领域正在迅速扩展,近年来相关出版物数量急剧增加。这些起源于内吞作用的小囊泡(30 - 100纳米)最初被认为是网织红细胞在成熟为红细胞过程中清除转铁蛋白受体的一种方式,后来被命名为外泌体。外泌体由晚期内体向内出芽形成多囊泡体(MVBs),并通过MVBs与质膜融合释放到细胞外环境中。自首次发现外泌体以来,已证明多种细胞均可释放这些囊泡。外泌体也已在包括血浆、鼻腔灌洗液、唾液和母乳在内的多种生物体液中被检测到。此外,研究表明外泌体的内容物和功能取决于其来源细胞以及产生它们的条件。外泌体已被证明具有多种功能,如诱导对过敏原的耐受性、消除小鼠体内已形成的肿瘤、抑制和激活自然杀伤细胞、促进向调节性T细胞的分化、刺激T细胞增殖以及诱导T细胞凋亡。2007年我们证明肥大细胞释放的外泌体含有信使核糖核酸(mRNA)和微小核糖核酸(miRNA),并且这些RNA可通过外泌体从一个细胞转运到另一个细胞。在受体细胞中,由外泌体转运的mRNA被证明可翻译成蛋白质,这表明所转运RNA具有调节功能。此外,我们还表明,源自氧化应激条件下生长细胞的外泌体可诱导受体细胞对进一步应激的耐受性,从而提示外泌体穿梭RNA的生物学功能。细胞培养基和生物体液中含有囊泡和脱落碎片的混合物。因此,一种高质量的外泌体分离方法,随后对外泌体及其内容物进行表征和鉴定,对于区分外泌体与其他囊泡和颗粒至关重要。在此,我们介绍一种从细胞培养基和体液中分离外泌体的方法。这种分离方法基于重复的离心和过滤步骤,最后进行超速离心步骤使外泌体沉淀。文中重点介绍了鉴定外泌体以及表征外泌体形态和蛋白质含量的重要方法,包括电子显微镜、流式细胞术和蛋白质免疫印迹法。外泌体总RNA的纯化基于离心柱层析法,并使用生物分析仪分析外泌体RNA的产量和大小分布。