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A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5
The central nervous system (CNS) has specific barriers that protect the brain from potential threats and tightly regulate molecular transport. Despite the critical functions of the CNS barriers, the mechanisms underlying their development and function are not well understood, and there are very limi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861362/ https://www.ncbi.nlm.nih.gov/pubmed/29437557 http://dx.doi.org/10.1242/bio.030494 |
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author | van Leeuwen, Lisanne Martine Evans, Robert J. Jim, Kin Ki Verboom, Theo Fang, Xiaoming Bojarczuk, Aleksandra Malicki, Jarema Johnston, Simon Andrew van der Sar, Astrid Marijke |
author_facet | van Leeuwen, Lisanne Martine Evans, Robert J. Jim, Kin Ki Verboom, Theo Fang, Xiaoming Bojarczuk, Aleksandra Malicki, Jarema Johnston, Simon Andrew van der Sar, Astrid Marijke |
author_sort | van Leeuwen, Lisanne Martine |
collection | PubMed |
description | The central nervous system (CNS) has specific barriers that protect the brain from potential threats and tightly regulate molecular transport. Despite the critical functions of the CNS barriers, the mechanisms underlying their development and function are not well understood, and there are very limited experimental models for their study. Claudin 5 is a tight junction protein required for blood brain barrier (BBB) and, probably, choroid plexus (CP) structure and function in vertebrates. Here, we show that the gene claudin 5a is the zebrafish orthologue with high fidelity expression, in the BBB and CP barriers, that demonstrates the conservation of the BBB and CP between humans and zebrafish. Expression of claudin 5a correlates with developmental tightening of the BBB and is restricted to a subset of the brain vasculature clearly delineating the BBB. We show that claudin 5a-expressing cells of the CP are ciliated ependymal cells that drive fluid flow in the brain ventricles. Finally, we find that CP development precedes BBB development and that claudin 5a expression occurs simultaneously with angiogenesis. Thus, our novel transgenic zebrafish represents an ideal model to study CNS barrier development and function, critical in understanding the mechanisms underlying CNS barrier function in health and disease. |
format | Online Article Text |
id | pubmed-5861362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58613622018-04-05 A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 van Leeuwen, Lisanne Martine Evans, Robert J. Jim, Kin Ki Verboom, Theo Fang, Xiaoming Bojarczuk, Aleksandra Malicki, Jarema Johnston, Simon Andrew van der Sar, Astrid Marijke Biol Open Research Article The central nervous system (CNS) has specific barriers that protect the brain from potential threats and tightly regulate molecular transport. Despite the critical functions of the CNS barriers, the mechanisms underlying their development and function are not well understood, and there are very limited experimental models for their study. Claudin 5 is a tight junction protein required for blood brain barrier (BBB) and, probably, choroid plexus (CP) structure and function in vertebrates. Here, we show that the gene claudin 5a is the zebrafish orthologue with high fidelity expression, in the BBB and CP barriers, that demonstrates the conservation of the BBB and CP between humans and zebrafish. Expression of claudin 5a correlates with developmental tightening of the BBB and is restricted to a subset of the brain vasculature clearly delineating the BBB. We show that claudin 5a-expressing cells of the CP are ciliated ependymal cells that drive fluid flow in the brain ventricles. Finally, we find that CP development precedes BBB development and that claudin 5a expression occurs simultaneously with angiogenesis. Thus, our novel transgenic zebrafish represents an ideal model to study CNS barrier development and function, critical in understanding the mechanisms underlying CNS barrier function in health and disease. The Company of Biologists Ltd 2018-02-15 /pmc/articles/PMC5861362/ /pubmed/29437557 http://dx.doi.org/10.1242/bio.030494 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article van Leeuwen, Lisanne Martine Evans, Robert J. Jim, Kin Ki Verboom, Theo Fang, Xiaoming Bojarczuk, Aleksandra Malicki, Jarema Johnston, Simon Andrew van der Sar, Astrid Marijke A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 |
title | A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 |
title_full | A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 |
title_fullStr | A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 |
title_full_unstemmed | A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 |
title_short | A transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 |
title_sort | transgenic zebrafish model for the in vivo study of the blood and choroid plexus brain barriers using claudin 5 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861362/ https://www.ncbi.nlm.nih.gov/pubmed/29437557 http://dx.doi.org/10.1242/bio.030494 |
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