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Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system
Crossing the blood–brain and the blood–cerebrospinal fluid barriers (BCSFB) is one of the fundamental challenges in the development of new therapeutic molecules for brain disorders because these barriers prevent entry of most drugs from the blood into the brain. However, some large molecules, like t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596253/ https://www.ncbi.nlm.nih.gov/pubmed/26491705 http://dx.doi.org/10.1038/mtm.2015.37 |
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author | Méndez-Gómez, Héctor R Galera-Prat, Albert Meyers, Craig Chen, Weijun Singh, Jasbir Carrión-Vázquez, Mariano Muzyczka, Nicholas |
author_facet | Méndez-Gómez, Héctor R Galera-Prat, Albert Meyers, Craig Chen, Weijun Singh, Jasbir Carrión-Vázquez, Mariano Muzyczka, Nicholas |
author_sort | Méndez-Gómez, Héctor R |
collection | PubMed |
description | Crossing the blood–brain and the blood–cerebrospinal fluid barriers (BCSFB) is one of the fundamental challenges in the development of new therapeutic molecules for brain disorders because these barriers prevent entry of most drugs from the blood into the brain. However, some large molecules, like the protein transferrin, cross these barriers using a specific receptor that transports them into the brain. Based on this mechanism, we engineered a receptor/ligand system to overcome the brain barriers by combining the human transferrin receptor with the cohesin domain from Clostridium thermocellum, and we tested the hybrid receptor in the choroid plexus of the mouse brain with a dockerin ligand. By expressing our receptor in choroidal ependymocytes, which are part of the BCSFB, we found that our systemically administrated ligand was able to bind to the receptor and accumulate in ependymocytes, where some of the ligand was transported from the blood side to the brain side. |
format | Online Article Text |
id | pubmed-4596253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45962532015-10-21 Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system Méndez-Gómez, Héctor R Galera-Prat, Albert Meyers, Craig Chen, Weijun Singh, Jasbir Carrión-Vázquez, Mariano Muzyczka, Nicholas Mol Ther Methods Clin Dev Article Crossing the blood–brain and the blood–cerebrospinal fluid barriers (BCSFB) is one of the fundamental challenges in the development of new therapeutic molecules for brain disorders because these barriers prevent entry of most drugs from the blood into the brain. However, some large molecules, like the protein transferrin, cross these barriers using a specific receptor that transports them into the brain. Based on this mechanism, we engineered a receptor/ligand system to overcome the brain barriers by combining the human transferrin receptor with the cohesin domain from Clostridium thermocellum, and we tested the hybrid receptor in the choroid plexus of the mouse brain with a dockerin ligand. By expressing our receptor in choroidal ependymocytes, which are part of the BCSFB, we found that our systemically administrated ligand was able to bind to the receptor and accumulate in ependymocytes, where some of the ligand was transported from the blood side to the brain side. Nature Publishing Group 2015-10-07 /pmc/articles/PMC4596253/ /pubmed/26491705 http://dx.doi.org/10.1038/mtm.2015.37 Text en Copyright © 2015 Official journal of the American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Méndez-Gómez, Héctor R Galera-Prat, Albert Meyers, Craig Chen, Weijun Singh, Jasbir Carrión-Vázquez, Mariano Muzyczka, Nicholas Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system |
title | Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system |
title_full | Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system |
title_fullStr | Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system |
title_full_unstemmed | Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system |
title_short | Transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system |
title_sort | transcytosis in the blood–cerebrospinal fluid barrier of the mouse brain with an engineered receptor/ligand system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596253/ https://www.ncbi.nlm.nih.gov/pubmed/26491705 http://dx.doi.org/10.1038/mtm.2015.37 |
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