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An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases
INTRODUCTION: The neurovascular unit (NVU) – the interaction between the neurons and the cerebrovasculature – is increasingly important to interrogate through human-based experimental models. Although advanced models of cerebral capillaries have been developed in the last decade, there is currently...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678181/ https://www.ncbi.nlm.nih.gov/pubmed/33213497 http://dx.doi.org/10.1186/s13024-020-00418-z |
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author | Robert, Jerome Weilinger, Nicholas L. Cao, Li-Ping Cataldi, Stefano Button, Emily B. Stukas, Sophie Martin, Emma M. Seibler, Philip Gilmour, Megan Caffrey, Tara M. Rowe, Elyn M. Fan, Jianjia MacVicar, Brian Farrer, Matthew J. Wellington, Cheryl L. |
author_facet | Robert, Jerome Weilinger, Nicholas L. Cao, Li-Ping Cataldi, Stefano Button, Emily B. Stukas, Sophie Martin, Emma M. Seibler, Philip Gilmour, Megan Caffrey, Tara M. Rowe, Elyn M. Fan, Jianjia MacVicar, Brian Farrer, Matthew J. Wellington, Cheryl L. |
author_sort | Robert, Jerome |
collection | PubMed |
description | INTRODUCTION: The neurovascular unit (NVU) – the interaction between the neurons and the cerebrovasculature – is increasingly important to interrogate through human-based experimental models. Although advanced models of cerebral capillaries have been developed in the last decade, there is currently no in vitro 3-dimensional (3D) perfusible model of the human cortical arterial NVU. METHOD: We used a tissue-engineering technique to develop a scaffold-directed, perfusible, 3D human NVU that is cultured in native-like flow conditions that mimics the anatomy and physiology of cortical penetrating arteries. RESULTS: This system, composed of primary human vascular cells (endothelial cells, smooth muscle cells and astrocytes) and induced pluripotent stem cell (iPSC) derived neurons, demonstrates a physiological multilayer organization of the involved cell types. It reproduces key characteristics of cortical neurons and astrocytes and enables formation of a selective and functional endothelial barrier. We provide proof-of-principle data showing that this in vitro human arterial NVU may be suitable to study neurovascular components of neurodegenerative diseases such as Alzheimer’s disease (AD), as endogenously produced phosphorylated tau and beta-amyloid accumulate in the model over time. Finally, neuronal and glial fluid biomarkers relevant to neurodegenerative diseases are measurable in our arterial NVU model. CONCLUSION: This model is a suitable research tool to investigate arterial NVU functions in healthy and disease states. Further, the design of the platform allows culture under native-like flow conditions for extended periods of time and yields sufficient tissue and media for downstream immunohistochemistry and biochemistry analyses. |
format | Online Article Text |
id | pubmed-7678181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76781812020-11-20 An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases Robert, Jerome Weilinger, Nicholas L. Cao, Li-Ping Cataldi, Stefano Button, Emily B. Stukas, Sophie Martin, Emma M. Seibler, Philip Gilmour, Megan Caffrey, Tara M. Rowe, Elyn M. Fan, Jianjia MacVicar, Brian Farrer, Matthew J. Wellington, Cheryl L. Mol Neurodegener Research Article INTRODUCTION: The neurovascular unit (NVU) – the interaction between the neurons and the cerebrovasculature – is increasingly important to interrogate through human-based experimental models. Although advanced models of cerebral capillaries have been developed in the last decade, there is currently no in vitro 3-dimensional (3D) perfusible model of the human cortical arterial NVU. METHOD: We used a tissue-engineering technique to develop a scaffold-directed, perfusible, 3D human NVU that is cultured in native-like flow conditions that mimics the anatomy and physiology of cortical penetrating arteries. RESULTS: This system, composed of primary human vascular cells (endothelial cells, smooth muscle cells and astrocytes) and induced pluripotent stem cell (iPSC) derived neurons, demonstrates a physiological multilayer organization of the involved cell types. It reproduces key characteristics of cortical neurons and astrocytes and enables formation of a selective and functional endothelial barrier. We provide proof-of-principle data showing that this in vitro human arterial NVU may be suitable to study neurovascular components of neurodegenerative diseases such as Alzheimer’s disease (AD), as endogenously produced phosphorylated tau and beta-amyloid accumulate in the model over time. Finally, neuronal and glial fluid biomarkers relevant to neurodegenerative diseases are measurable in our arterial NVU model. CONCLUSION: This model is a suitable research tool to investigate arterial NVU functions in healthy and disease states. Further, the design of the platform allows culture under native-like flow conditions for extended periods of time and yields sufficient tissue and media for downstream immunohistochemistry and biochemistry analyses. BioMed Central 2020-11-19 /pmc/articles/PMC7678181/ /pubmed/33213497 http://dx.doi.org/10.1186/s13024-020-00418-z Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article Robert, Jerome Weilinger, Nicholas L. Cao, Li-Ping Cataldi, Stefano Button, Emily B. Stukas, Sophie Martin, Emma M. Seibler, Philip Gilmour, Megan Caffrey, Tara M. Rowe, Elyn M. Fan, Jianjia MacVicar, Brian Farrer, Matthew J. Wellington, Cheryl L. An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases |
title | An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases |
title_full | An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases |
title_fullStr | An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases |
title_full_unstemmed | An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases |
title_short | An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases |
title_sort | in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678181/ https://www.ncbi.nlm.nih.gov/pubmed/33213497 http://dx.doi.org/10.1186/s13024-020-00418-z |
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