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Extracellular vesicles through the blood–brain barrier: a review
Extracellular vesicles (EVs) are particles naturally released from cells that are delimited by a lipid bilayer and are unable to replicate. How the EVs cross the Blood–Brain barrier (BBB) in a bidirectional manner between the bloodstream and brain parenchyma remains poorly understood. Most in vitro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310691/ https://www.ncbi.nlm.nih.gov/pubmed/35879759 http://dx.doi.org/10.1186/s12987-022-00359-3 |
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author | Ramos-Zaldívar, Héctor M. Polakovicova, Iva Salas-Huenuleo, Edison Corvalán, Alejandro H. Kogan, Marcelo J. Yefi, Claudia P. Andia, Marcelo E. |
author_facet | Ramos-Zaldívar, Héctor M. Polakovicova, Iva Salas-Huenuleo, Edison Corvalán, Alejandro H. Kogan, Marcelo J. Yefi, Claudia P. Andia, Marcelo E. |
author_sort | Ramos-Zaldívar, Héctor M. |
collection | PubMed |
description | Extracellular vesicles (EVs) are particles naturally released from cells that are delimited by a lipid bilayer and are unable to replicate. How the EVs cross the Blood–Brain barrier (BBB) in a bidirectional manner between the bloodstream and brain parenchyma remains poorly understood. Most in vitro models that have evaluated this event have relied on monolayer transwell or microfluidic organ-on-a-chip techniques that do not account for the combined effect of all cellular layers that constitute the BBB at different sites of the Central Nervous System. There has not been direct transcytosis visualization through the BBB in mammals in vivo, and evidence comes from in vivo experiments in zebrafish. Literature is scarce on this topic, and techniques describing the mechanisms of EVs motion through the BBB are inconsistent. This review will focus on in vitro and in vivo methodologies used to evaluate EVs transcytosis, how EVs overcome this fundamental structure, and discuss potential methodological approaches for future analyses to clarify these issues. Understanding how EVs cross the BBB will be essential for their future use as vehicles in pharmacology and therapeutics. |
format | Online Article Text |
id | pubmed-9310691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93106912022-07-26 Extracellular vesicles through the blood–brain barrier: a review Ramos-Zaldívar, Héctor M. Polakovicova, Iva Salas-Huenuleo, Edison Corvalán, Alejandro H. Kogan, Marcelo J. Yefi, Claudia P. Andia, Marcelo E. Fluids Barriers CNS Review Extracellular vesicles (EVs) are particles naturally released from cells that are delimited by a lipid bilayer and are unable to replicate. How the EVs cross the Blood–Brain barrier (BBB) in a bidirectional manner between the bloodstream and brain parenchyma remains poorly understood. Most in vitro models that have evaluated this event have relied on monolayer transwell or microfluidic organ-on-a-chip techniques that do not account for the combined effect of all cellular layers that constitute the BBB at different sites of the Central Nervous System. There has not been direct transcytosis visualization through the BBB in mammals in vivo, and evidence comes from in vivo experiments in zebrafish. Literature is scarce on this topic, and techniques describing the mechanisms of EVs motion through the BBB are inconsistent. This review will focus on in vitro and in vivo methodologies used to evaluate EVs transcytosis, how EVs overcome this fundamental structure, and discuss potential methodological approaches for future analyses to clarify these issues. Understanding how EVs cross the BBB will be essential for their future use as vehicles in pharmacology and therapeutics. BioMed Central 2022-07-25 /pmc/articles/PMC9310691/ /pubmed/35879759 http://dx.doi.org/10.1186/s12987-022-00359-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Ramos-Zaldívar, Héctor M. Polakovicova, Iva Salas-Huenuleo, Edison Corvalán, Alejandro H. Kogan, Marcelo J. Yefi, Claudia P. Andia, Marcelo E. Extracellular vesicles through the blood–brain barrier: a review |
title | Extracellular vesicles through the blood–brain barrier: a review |
title_full | Extracellular vesicles through the blood–brain barrier: a review |
title_fullStr | Extracellular vesicles through the blood–brain barrier: a review |
title_full_unstemmed | Extracellular vesicles through the blood–brain barrier: a review |
title_short | Extracellular vesicles through the blood–brain barrier: a review |
title_sort | extracellular vesicles through the blood–brain barrier: a review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310691/ https://www.ncbi.nlm.nih.gov/pubmed/35879759 http://dx.doi.org/10.1186/s12987-022-00359-3 |
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