CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow Cytometry

The quantification of the specific disease-associated populations of circulating extracellular membrane nanovesicles (ENVs) has opened up new opportunities for liquid biopsy in cancer and other chronic diseases. However, the sensitivity of such methods is mediated by an optimal combination of the is...

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Published in:Membranes
Main Authors: Nadezhda Nikiforova, Maria Chumachenko, Inga Nazarova, Lidia Zabegina, Maria Slyusarenko, Elena Sidina, Anastasia Malek
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Subjects:
Online Access:https://www.mdpi.com/2077-0375/11/7/526
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author Nadezhda Nikiforova
Maria Chumachenko
Inga Nazarova
Lidia Zabegina
Maria Slyusarenko
Elena Sidina
Anastasia Malek
author_facet Nadezhda Nikiforova
Maria Chumachenko
Inga Nazarova
Lidia Zabegina
Maria Slyusarenko
Elena Sidina
Anastasia Malek
author_sort Nadezhda Nikiforova
collection DOAJ
container_title Membranes
description The quantification of the specific disease-associated populations of circulating extracellular membrane nanovesicles (ENVs) has opened up new opportunities for liquid biopsy in cancer and other chronic diseases. However, the sensitivity of such methods is mediated by an optimal combination of the isolation and labeling approaches, and is not yet sufficient for routine clinical application. The presented study aimed to develop, characterize, and explore a new approach to non-specific ENV staining, followed by size-exclusive chromatography (SEC), which allows us to increase the sensitivity of bead-assisted flow cytometry. Plasma from healthy donors was purified from large components, stained with lipophilic CM-Dil dye, and fractionated by means of SEC. The obtained fractions were analyzed in terms of particle size and concentration using NTA, as well as vesicular markers and plasma protein content via dot-blotting. We characterized the process of CM-Dil-stained plasma fractionation in detail and indicated the fractions with optimal characteristics. Finally, we explored the sensitivity of on-bead flow cytometry for the analysis of specific populations of plasma ENVs and demonstrated the advantages and limitations of the proposed technique.
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spelling doaj-art-e148bc5f21994cf289f2f8ff881060e22025-08-19T22:46:32ZengMDPI AGMembranes2077-03752021-07-0111752610.3390/membranes11070526CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow CytometryNadezhda Nikiforova0Maria Chumachenko1Inga Nazarova2Lidia Zabegina3Maria Slyusarenko4Elena Sidina5Anastasia Malek6Subcellular Technology Laboratory, N.N. Petrov National Medical Center of Oncology, 197758 St. Petersburg, RussiaDepartment of Biochemistry, Belarusian State University, 220030 Minsk, BelarusSubcellular Technology Laboratory, N.N. Petrov National Medical Center of Oncology, 197758 St. Petersburg, RussiaSubcellular Technology Laboratory, N.N. Petrov National Medical Center of Oncology, 197758 St. Petersburg, RussiaSubcellular Technology Laboratory, N.N. Petrov National Medical Center of Oncology, 197758 St. Petersburg, RussiaSubcellular Technology Laboratory, N.N. Petrov National Medical Center of Oncology, 197758 St. Petersburg, RussiaSubcellular Technology Laboratory, N.N. Petrov National Medical Center of Oncology, 197758 St. Petersburg, RussiaThe quantification of the specific disease-associated populations of circulating extracellular membrane nanovesicles (ENVs) has opened up new opportunities for liquid biopsy in cancer and other chronic diseases. However, the sensitivity of such methods is mediated by an optimal combination of the isolation and labeling approaches, and is not yet sufficient for routine clinical application. The presented study aimed to develop, characterize, and explore a new approach to non-specific ENV staining, followed by size-exclusive chromatography (SEC), which allows us to increase the sensitivity of bead-assisted flow cytometry. Plasma from healthy donors was purified from large components, stained with lipophilic CM-Dil dye, and fractionated by means of SEC. The obtained fractions were analyzed in terms of particle size and concentration using NTA, as well as vesicular markers and plasma protein content via dot-blotting. We characterized the process of CM-Dil-stained plasma fractionation in detail and indicated the fractions with optimal characteristics. Finally, we explored the sensitivity of on-bead flow cytometry for the analysis of specific populations of plasma ENVs and demonstrated the advantages and limitations of the proposed technique.https://www.mdpi.com/2077-0375/11/7/526extracellular vesiclesplasmaCM-Dillabelingsize exclusion chromatographySEC
spellingShingle Nadezhda Nikiforova
Maria Chumachenko
Inga Nazarova
Lidia Zabegina
Maria Slyusarenko
Elena Sidina
Anastasia Malek
CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow Cytometry
extracellular vesicles
plasma
CM-Dil
labeling
size exclusion chromatography
SEC
title CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow Cytometry
title_full CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow Cytometry
title_fullStr CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow Cytometry
title_full_unstemmed CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow Cytometry
title_short CM-Dil Staining and SEC of Plasma as an Approach to Increase Sensitivity of Extracellular Nanovesicles Quantification by Bead-Assisted Flow Cytometry
title_sort cm dil staining and sec of plasma as an approach to increase sensitivity of extracellular nanovesicles quantification by bead assisted flow cytometry
topic extracellular vesicles
plasma
CM-Dil
labeling
size exclusion chromatography
SEC
url https://www.mdpi.com/2077-0375/11/7/526
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