Improved Characterization of EV Preparations Based on Protein to Lipid Ratio and Lipid Properties |
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| Authors: | Xabier Osteikoetxea Andrea Balogh Katalin Szabó-Taylor Andrea Németh Tamás Géza Szabó Krisztina Pálóczi Barbara Sódar ágnes Kittel Bence Gy?rgy éva Pállinger János Matkó Edit Irén Buzás |
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| Institution: | 1. Department of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.; 2. Department of Immunology, Eötvös Loránd University, Budapest, Hungary.; 3. Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.; 4. Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts, United States of America.; University of Edinburgh, UNITED KINGDOM, |
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| Abstract: | In recent years the study of extracellular vesicles has gathered much scientific and clinical interest. As the field is expanding, it is becoming clear that better methods for characterization and quantification of extracellular vesicles as well as better standards to compare studies are warranted. The goal of the present work was to find improved parameters to characterize extracellular vesicle preparations. Here we introduce a simple 96 well plate-based total lipid assay for determination of lipid content and protein to lipid ratios of extracellular vesicle preparations from various myeloid and lymphoid cell lines as well as blood plasma. These preparations included apoptotic bodies, microvesicles/microparticles, and exosomes isolated by size-based fractionation. We also investigated lipid bilayer order of extracellular vesicle subpopulations using Di-4-ANEPPDHQ lipid probe, and lipid composition using affinity reagents to clustered cholesterol (monoclonal anti-cholesterol antibody) and ganglioside GM1 (cholera toxin subunit B). We have consistently found different protein to lipid ratios characteristic for the investigated extracellular vesicle subpopulations which were substantially altered in the case of vesicular damage or protein contamination. Spectral ratiometric imaging and flow cytometric analysis also revealed marked differences between the various vesicle populations in their lipid order and their clustered membrane cholesterol and GM1 content. Our study introduces for the first time a simple and readily available lipid assay to complement the widely used protein assays in order to better characterize extracellular vesicle preparations. Besides differentiating extracellular vesicle subpopulations, the novel parameters introduced in this work (protein to lipid ratio, lipid bilayer order, and lipid composition), may prove useful for quality control of extracellular vesicle related basic and clinical studies. |
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