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The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator
BACKGROUND: In the vascular compartment, the serine protease tissue-type plasminogen activator (tPA) promotes fibrinolysis, justifying its clinical use against vasculo-occlusive diseases. Accumulating evidence shows that circulating tPA (endogenous or exogenous) also controls brain physiopathologica...
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/PMC9569045/ https://www.ncbi.nlm.nih.gov/pubmed/36243724 http://dx.doi.org/10.1186/s12987-022-00378-0 |
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author | Zuba, Vincent Furon, Jonathane Bellemain-Sagnard, Mathys Martinez de Lazarrondo, Sara Lebouvier, Laurent Rubio, Marina Hommet, Yannick Gauberti, Maxime Vivien, Denis Ali, Carine |
author_facet | Zuba, Vincent Furon, Jonathane Bellemain-Sagnard, Mathys Martinez de Lazarrondo, Sara Lebouvier, Laurent Rubio, Marina Hommet, Yannick Gauberti, Maxime Vivien, Denis Ali, Carine |
author_sort | Zuba, Vincent |
collection | PubMed |
description | BACKGROUND: In the vascular compartment, the serine protease tissue-type plasminogen activator (tPA) promotes fibrinolysis, justifying its clinical use against vasculo-occlusive diseases. Accumulating evidence shows that circulating tPA (endogenous or exogenous) also controls brain physiopathological processes, like cerebrovascular reactivity, blood–brain barrier (BBB) homeostasis, inflammation and neuronal fate. Whether this occurs by direct actions on parenchymal cells and/or indirectly via barriers between the blood and the central nervous system (CNS) remains unclear. Here, we postulated that vascular tPA can reach the brain parenchyma via the blood-cerebrospinal fluid barrier (BCSFB), that relies on choroid plexus (CP) epithelial cells (CPECs). METHODS: We produced various reporter fusion proteins to track tPA in primary cultures of CPECs, in CP explants and in vivo in mice. We also investigated the mechanisms underlying tPA transport across the BCSFB, with pharmacological and molecular approaches. RESULTS: We first demonstrated that tPA can be internalized by CPECs in primary cultures and in ex vivo CPs explants. In vivo, tPA can also be internalized by CPECs both at their basal and apical sides. After intra-vascular administration, tPA can reach the cerebral spinal fluid (CSF) and the brain parenchyma. Further investigation allowed discovering that the transcytosis of tPA is mediated by Low-density-Lipoprotein Related Protein-1 (LRP1) expressed at the surface of CPECs and depends on the finger domain of tPA. Interestingly, albumin, which has a size comparable to that of tPA, does not normally cross the CPs, but switches to a transportable form when grafted to the finger domain of tPA. CONCLUSIONS: These findings provide new insights on how vascular tPA can reach the brain parenchyma, and open therapeutic avenues for CNS disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-022-00378-0. |
format | Online Article Text |
id | pubmed-9569045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95690452022-10-16 The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator Zuba, Vincent Furon, Jonathane Bellemain-Sagnard, Mathys Martinez de Lazarrondo, Sara Lebouvier, Laurent Rubio, Marina Hommet, Yannick Gauberti, Maxime Vivien, Denis Ali, Carine Fluids Barriers CNS Research BACKGROUND: In the vascular compartment, the serine protease tissue-type plasminogen activator (tPA) promotes fibrinolysis, justifying its clinical use against vasculo-occlusive diseases. Accumulating evidence shows that circulating tPA (endogenous or exogenous) also controls brain physiopathological processes, like cerebrovascular reactivity, blood–brain barrier (BBB) homeostasis, inflammation and neuronal fate. Whether this occurs by direct actions on parenchymal cells and/or indirectly via barriers between the blood and the central nervous system (CNS) remains unclear. Here, we postulated that vascular tPA can reach the brain parenchyma via the blood-cerebrospinal fluid barrier (BCSFB), that relies on choroid plexus (CP) epithelial cells (CPECs). METHODS: We produced various reporter fusion proteins to track tPA in primary cultures of CPECs, in CP explants and in vivo in mice. We also investigated the mechanisms underlying tPA transport across the BCSFB, with pharmacological and molecular approaches. RESULTS: We first demonstrated that tPA can be internalized by CPECs in primary cultures and in ex vivo CPs explants. In vivo, tPA can also be internalized by CPECs both at their basal and apical sides. After intra-vascular administration, tPA can reach the cerebral spinal fluid (CSF) and the brain parenchyma. Further investigation allowed discovering that the transcytosis of tPA is mediated by Low-density-Lipoprotein Related Protein-1 (LRP1) expressed at the surface of CPECs and depends on the finger domain of tPA. Interestingly, albumin, which has a size comparable to that of tPA, does not normally cross the CPs, but switches to a transportable form when grafted to the finger domain of tPA. CONCLUSIONS: These findings provide new insights on how vascular tPA can reach the brain parenchyma, and open therapeutic avenues for CNS disorders. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-022-00378-0. BioMed Central 2022-10-15 /pmc/articles/PMC9569045/ /pubmed/36243724 http://dx.doi.org/10.1186/s12987-022-00378-0 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 | Research Zuba, Vincent Furon, Jonathane Bellemain-Sagnard, Mathys Martinez de Lazarrondo, Sara Lebouvier, Laurent Rubio, Marina Hommet, Yannick Gauberti, Maxime Vivien, Denis Ali, Carine The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator |
title | The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator |
title_full | The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator |
title_fullStr | The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator |
title_full_unstemmed | The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator |
title_short | The choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator |
title_sort | choroid plexus: a door between the blood and the brain for tissue-type plasminogen activator |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569045/ https://www.ncbi.nlm.nih.gov/pubmed/36243724 http://dx.doi.org/10.1186/s12987-022-00378-0 |
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