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Exosome isolation from distinct biofluids using precipitation and column-based approaches
The potential of exosomes as biomarker resources for diagnostics, prognostics and even for therapeutics is an area of intense research. Despite the various approaches available, there is no consensus with respect to the best methodology for isolating exosomes and to provide substantial yields with r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995457/ https://www.ncbi.nlm.nih.gov/pubmed/29889903 http://dx.doi.org/10.1371/journal.pone.0198820 |
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author | Soares Martins, Tânia Catita, José Martins Rosa, Ilka A. B. da Cruz e Silva, Odete Henriques, Ana Gabriela |
author_facet | Soares Martins, Tânia Catita, José Martins Rosa, Ilka A. B. da Cruz e Silva, Odete Henriques, Ana Gabriela |
author_sort | Soares Martins, Tânia |
collection | PubMed |
description | The potential of exosomes as biomarker resources for diagnostics, prognostics and even for therapeutics is an area of intense research. Despite the various approaches available, there is no consensus with respect to the best methodology for isolating exosomes and to provide substantial yields with reliable quality. Differential centrifugation is the most commonly used method but it is time-consuming and requires large sample volumes, thus alternative methods are urgently needed. In this study two precipitation-based methods and one column-based approach were compared for exosome isolation from distinct biofluids (serum, plasma and cerebrospinal fluid). Exosome characterization included morphological analyses, determination of particle concentration, stability and exosome preparations’ purity, using different complementary approaches such as Nanoparticle Tracking Analysis, Electrophoretic Light Scattering, Transmission Electron Microscopy, EXOCET colorimetric assay, protein quantification methods and western blotting. The three commercial kits tested successfully isolated exosomes from the biofluids under study, although ExoS showed the best performance in terms of exosome yield and purity. Data shows that methods other than differential centrifugation can be applied to quickly and efficiently isolate exosomes from reduced biofluid volumes. The possibility to use small volumes is fundamental in the context of translational and clinical research, thus the results here presented contribute significantly in this respect. |
format | Online Article Text |
id | pubmed-5995457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59954572018-06-21 Exosome isolation from distinct biofluids using precipitation and column-based approaches Soares Martins, Tânia Catita, José Martins Rosa, Ilka A. B. da Cruz e Silva, Odete Henriques, Ana Gabriela PLoS One Research Article The potential of exosomes as biomarker resources for diagnostics, prognostics and even for therapeutics is an area of intense research. Despite the various approaches available, there is no consensus with respect to the best methodology for isolating exosomes and to provide substantial yields with reliable quality. Differential centrifugation is the most commonly used method but it is time-consuming and requires large sample volumes, thus alternative methods are urgently needed. In this study two precipitation-based methods and one column-based approach were compared for exosome isolation from distinct biofluids (serum, plasma and cerebrospinal fluid). Exosome characterization included morphological analyses, determination of particle concentration, stability and exosome preparations’ purity, using different complementary approaches such as Nanoparticle Tracking Analysis, Electrophoretic Light Scattering, Transmission Electron Microscopy, EXOCET colorimetric assay, protein quantification methods and western blotting. The three commercial kits tested successfully isolated exosomes from the biofluids under study, although ExoS showed the best performance in terms of exosome yield and purity. Data shows that methods other than differential centrifugation can be applied to quickly and efficiently isolate exosomes from reduced biofluid volumes. The possibility to use small volumes is fundamental in the context of translational and clinical research, thus the results here presented contribute significantly in this respect. Public Library of Science 2018-06-11 /pmc/articles/PMC5995457/ /pubmed/29889903 http://dx.doi.org/10.1371/journal.pone.0198820 Text en © 2018 Soares Martins et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Soares Martins, Tânia Catita, José Martins Rosa, Ilka A. B. da Cruz e Silva, Odete Henriques, Ana Gabriela Exosome isolation from distinct biofluids using precipitation and column-based approaches |
title | Exosome isolation from distinct biofluids using precipitation and column-based approaches |
title_full | Exosome isolation from distinct biofluids using precipitation and column-based approaches |
title_fullStr | Exosome isolation from distinct biofluids using precipitation and column-based approaches |
title_full_unstemmed | Exosome isolation from distinct biofluids using precipitation and column-based approaches |
title_short | Exosome isolation from distinct biofluids using precipitation and column-based approaches |
title_sort | exosome isolation from distinct biofluids using precipitation and column-based approaches |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995457/ https://www.ncbi.nlm.nih.gov/pubmed/29889903 http://dx.doi.org/10.1371/journal.pone.0198820 |
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