Abstract OR-20: Visualization of Exosomes Using Transmission Electron Microscopy and Immunogold Labelling
| Autor: | Svetlana E. Semina, Anna A Vnukova, Dmitry V. Bagrov, Evgeniy G. Evtushenko |
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| Rok vydání: | 2019 |
| Předmět: |
General Immunology and Microbiology
Chemistry General Neuroscience nanotracking analysis lcsh:R immunogold labeling lcsh:Medicine exosomes Immunogold labelling General Biochemistry Genetics and Molecular Biology Microvesicles Visualization Transmission electron microscopy transmission electron microscopy Biophysics |
| Zdroj: | International Journal of Biomedicine, Vol 9, Iss Suppl_1, Pp S14-S14 (2019) |
| ISSN: | 2158-0529 2158-0510 |
| DOI: | 10.21103/ijbm.9.suppl_1.or20 |
| Popis: | Background: Extracellular vesicles are small membrane particles which are produced by the cells and released into the surrounding space. They can transfer biomolecules into recipient cells. The typical vesicle size is 100-1000 nm, so transmission electron microscopy (TEM) is the most suitable tool for their visualization. This is especially true for the smallest vesicles – the exosomes with the size below 200 nm. Methods: We isolated exosomes produced by MCF-7 cancer cells and the two drug-resistant MCF-7 sublines (Semina et.al., Molecules, 2018). The exosomes were isolated from the conditioned medium by ultracentrifugation, and their size was measured by nanotracking analysis (NTA) and TEM. Immunogold labelling was carried out on exosomes deposited onto carbon TEM grids. It involved the following principal steps: the vesicle deposition, sample treatment by the anti-CD9 antibodies, sample treatment by the 10 nm colloidal gold nanoparticles conjugated with protein A, staining with uranyl acetate. Washing and blocking steps were done between the principal ones. The samples were imaged using a JEM-1011 microscope at 80 kV. Results: NTA and TEM yielded similar results – the exosomes produced by the three studied cell lines had the almost equal size in the range from 50 to 200 nm. When imaged by TEM, most exosomes demonstrated the typical cup-shaped morphology. We used immunogold labelling to verify that the exosomes carried the CD9 marker on them (Fig. 1). We achieved the labelling specificity in the range of 8-10; this value was calculated as the ratio of the surface densities of the exosome-bound labels (colloidal gold nanoparticles) and the non-specific background ones. Conclusion: We hope that the sample preparation and imaging procedures that we used could be useful for the investigation of other extracellular vesicles. |
| Databáze: | OpenAIRE |
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