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Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier
Exosomes are vesicles involved in intercellular communication. Their membrane structure and core content is largely dependent on the cell of origin. Exosomes have been investigated both for their biological roles and their possible use as disease biomarkers and drug carriers. These potential technol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505448/ https://www.ncbi.nlm.nih.gov/pubmed/32956358 http://dx.doi.org/10.1371/journal.pone.0232442 |
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author | Jakubec, Martin Maple-Grødem, Jodi Akbari, Saleha Nesse, Susanne Halskau, Øyvind Mork-Jansson, Astrid Elisabeth |
author_facet | Jakubec, Martin Maple-Grødem, Jodi Akbari, Saleha Nesse, Susanne Halskau, Øyvind Mork-Jansson, Astrid Elisabeth |
author_sort | Jakubec, Martin |
collection | PubMed |
description | Exosomes are vesicles involved in intercellular communication. Their membrane structure and core content is largely dependent on the cell of origin. Exosomes have been investigated both for their biological roles and their possible use as disease biomarkers and drug carriers. These potential technological applications require the rigorous characterization of exosomal blood brain barrier permeability and a description of their lipid bilayer composition. To achieve these goals, we have established a 3D static blood brain barrier system based on existing systems for liposomes and a complementary LC-MS/MS and (31)P nuclear magnetic resonance methodology for the analysis of purified human plasma-derived exosome-like vesicles. Results show that the isolated vesicles pass the blood brain barrier and are taken up in endothelial cells. The compositional analysis revealed that the isolated vesicles are enriched in lyso phospholipids and do not contain phosphatidylserine. These findings deviate significantly from the composition of exosomes originating from cell culture, and may reflect active removal by macrophages that respond to exposed phosphahtidylserine. |
format | Online Article Text |
id | pubmed-7505448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75054482020-09-30 Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier Jakubec, Martin Maple-Grødem, Jodi Akbari, Saleha Nesse, Susanne Halskau, Øyvind Mork-Jansson, Astrid Elisabeth PLoS One Research Article Exosomes are vesicles involved in intercellular communication. Their membrane structure and core content is largely dependent on the cell of origin. Exosomes have been investigated both for their biological roles and their possible use as disease biomarkers and drug carriers. These potential technological applications require the rigorous characterization of exosomal blood brain barrier permeability and a description of their lipid bilayer composition. To achieve these goals, we have established a 3D static blood brain barrier system based on existing systems for liposomes and a complementary LC-MS/MS and (31)P nuclear magnetic resonance methodology for the analysis of purified human plasma-derived exosome-like vesicles. Results show that the isolated vesicles pass the blood brain barrier and are taken up in endothelial cells. The compositional analysis revealed that the isolated vesicles are enriched in lyso phospholipids and do not contain phosphatidylserine. These findings deviate significantly from the composition of exosomes originating from cell culture, and may reflect active removal by macrophages that respond to exposed phosphahtidylserine. Public Library of Science 2020-09-21 /pmc/articles/PMC7505448/ /pubmed/32956358 http://dx.doi.org/10.1371/journal.pone.0232442 Text en © 2020 Jakubec 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 Jakubec, Martin Maple-Grødem, Jodi Akbari, Saleha Nesse, Susanne Halskau, Øyvind Mork-Jansson, Astrid Elisabeth Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier |
title | Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier |
title_full | Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier |
title_fullStr | Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier |
title_full_unstemmed | Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier |
title_short | Plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier |
title_sort | plasma-derived exosome-like vesicles are enriched in lyso-phospholipids and pass the blood-brain barrier |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505448/ https://www.ncbi.nlm.nih.gov/pubmed/32956358 http://dx.doi.org/10.1371/journal.pone.0232442 |
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