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Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment
Exosomes are cell-derived nanovesicles (50–150 nm), which mediate intercellular communication, and are candidate therapeutic agents. However, inefficiency of exosomal message transfer, such as mRNA, and lack of methods to create designer exosomes have hampered their development into therapeutic inte...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880805/ https://www.ncbi.nlm.nih.gov/pubmed/29610454 http://dx.doi.org/10.1038/s41467-018-03733-8 |
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author | Kojima, Ryosuke Bojar, Daniel Rizzi, Giorgio Hamri, Ghislaine Charpin-El El-Baba, Marie Daoud Saxena, Pratik Ausländer, Simon Tan, Kelly R. Fussenegger, Martin |
author_facet | Kojima, Ryosuke Bojar, Daniel Rizzi, Giorgio Hamri, Ghislaine Charpin-El El-Baba, Marie Daoud Saxena, Pratik Ausländer, Simon Tan, Kelly R. Fussenegger, Martin |
author_sort | Kojima, Ryosuke |
collection | PubMed |
description | Exosomes are cell-derived nanovesicles (50–150 nm), which mediate intercellular communication, and are candidate therapeutic agents. However, inefficiency of exosomal message transfer, such as mRNA, and lack of methods to create designer exosomes have hampered their development into therapeutic interventions. Here, we report a set of EXOsomal transfer into cells (EXOtic) devices that enable efficient, customizable production of designer exosomes in engineered mammalian cells. These genetically encoded devices in exosome producer cells enhance exosome production, specific mRNA packaging, and delivery of the mRNA into the cytosol of target cells, enabling efficient cell-to-cell communication without the need to concentrate exosomes. Further, engineered producer cells implanted in living mice could consistently deliver cargo mRNA to the brain. Therapeutic catalase mRNA delivery by designer exosomes attenuated neurotoxicity and neuroinflammation in in vitro and in vivo models of Parkinson’s disease, indicating the potential usefulness of the EXOtic devices for RNA delivery-based therapeutic applications. |
format | Online Article Text |
id | pubmed-5880805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58808052018-04-04 Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment Kojima, Ryosuke Bojar, Daniel Rizzi, Giorgio Hamri, Ghislaine Charpin-El El-Baba, Marie Daoud Saxena, Pratik Ausländer, Simon Tan, Kelly R. Fussenegger, Martin Nat Commun Article Exosomes are cell-derived nanovesicles (50–150 nm), which mediate intercellular communication, and are candidate therapeutic agents. However, inefficiency of exosomal message transfer, such as mRNA, and lack of methods to create designer exosomes have hampered their development into therapeutic interventions. Here, we report a set of EXOsomal transfer into cells (EXOtic) devices that enable efficient, customizable production of designer exosomes in engineered mammalian cells. These genetically encoded devices in exosome producer cells enhance exosome production, specific mRNA packaging, and delivery of the mRNA into the cytosol of target cells, enabling efficient cell-to-cell communication without the need to concentrate exosomes. Further, engineered producer cells implanted in living mice could consistently deliver cargo mRNA to the brain. Therapeutic catalase mRNA delivery by designer exosomes attenuated neurotoxicity and neuroinflammation in in vitro and in vivo models of Parkinson’s disease, indicating the potential usefulness of the EXOtic devices for RNA delivery-based therapeutic applications. Nature Publishing Group UK 2018-04-03 /pmc/articles/PMC5880805/ /pubmed/29610454 http://dx.doi.org/10.1038/s41467-018-03733-8 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kojima, Ryosuke Bojar, Daniel Rizzi, Giorgio Hamri, Ghislaine Charpin-El El-Baba, Marie Daoud Saxena, Pratik Ausländer, Simon Tan, Kelly R. Fussenegger, Martin Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment |
title | Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment |
title_full | Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment |
title_fullStr | Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment |
title_full_unstemmed | Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment |
title_short | Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment |
title_sort | designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for parkinson’s disease treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880805/ https://www.ncbi.nlm.nih.gov/pubmed/29610454 http://dx.doi.org/10.1038/s41467-018-03733-8 |
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