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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...

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Autores principales: Jakubec, Martin, Maple-Grødem, Jodi, Akbari, Saleha, Nesse, Susanne, Halskau, Øyvind, Mork-Jansson, Astrid Elisabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
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.
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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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