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Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells

The neurovascular unit (NVU) is composed of neurons, astrocytes, pericytes, and endothelial cells that form the blood–brain barrier (BBB). The NVU regulates material exchange between the bloodstream and the brain parenchyma, and its dysfunction is a primary or secondary cause of many cerebrovascular...

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Autores principales: Bosworth, Allison M., Faley, Shannon L., Bellan, Leon M., Lippmann, Ethan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797533/
https://www.ncbi.nlm.nih.gov/pubmed/29441348
http://dx.doi.org/10.3389/fbioe.2017.00087
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author Bosworth, Allison M.
Faley, Shannon L.
Bellan, Leon M.
Lippmann, Ethan S.
author_facet Bosworth, Allison M.
Faley, Shannon L.
Bellan, Leon M.
Lippmann, Ethan S.
author_sort Bosworth, Allison M.
collection PubMed
description The neurovascular unit (NVU) is composed of neurons, astrocytes, pericytes, and endothelial cells that form the blood–brain barrier (BBB). The NVU regulates material exchange between the bloodstream and the brain parenchyma, and its dysfunction is a primary or secondary cause of many cerebrovascular and neurodegenerative disorders. As such, there are substantial research thrusts in academia and industry toward building NVU models that mimic endogenous organization and function, which could be used to better understand disease mechanisms and assess drug efficacy. Human pluripotent stem cells, which can self-renew indefinitely and differentiate to almost any cell type in the body, are attractive for these models because they can provide a limitless source of individual cells from the NVU. In addition, human-induced pluripotent stem cells (iPSCs) offer the opportunity to build NVU models with an explicit genetic background and in the context of disease susceptibility. Herein, we review how iPSCs are being used to model neurovascular and neurodegenerative diseases, with particular focus on contributions of the BBB, and discuss existing technologies and emerging opportunities to merge these iPSC progenies with biomaterials platforms to create complex NVU systems that recreate the in vivo microenvironment.
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spelling pubmed-57975332018-02-13 Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells Bosworth, Allison M. Faley, Shannon L. Bellan, Leon M. Lippmann, Ethan S. Front Bioeng Biotechnol Bioengineering and Biotechnology The neurovascular unit (NVU) is composed of neurons, astrocytes, pericytes, and endothelial cells that form the blood–brain barrier (BBB). The NVU regulates material exchange between the bloodstream and the brain parenchyma, and its dysfunction is a primary or secondary cause of many cerebrovascular and neurodegenerative disorders. As such, there are substantial research thrusts in academia and industry toward building NVU models that mimic endogenous organization and function, which could be used to better understand disease mechanisms and assess drug efficacy. Human pluripotent stem cells, which can self-renew indefinitely and differentiate to almost any cell type in the body, are attractive for these models because they can provide a limitless source of individual cells from the NVU. In addition, human-induced pluripotent stem cells (iPSCs) offer the opportunity to build NVU models with an explicit genetic background and in the context of disease susceptibility. Herein, we review how iPSCs are being used to model neurovascular and neurodegenerative diseases, with particular focus on contributions of the BBB, and discuss existing technologies and emerging opportunities to merge these iPSC progenies with biomaterials platforms to create complex NVU systems that recreate the in vivo microenvironment. Frontiers Media S.A. 2018-01-30 /pmc/articles/PMC5797533/ /pubmed/29441348 http://dx.doi.org/10.3389/fbioe.2017.00087 Text en Copyright © 2018 Bosworth, Faley, Bellan and Lippmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Bosworth, Allison M.
Faley, Shannon L.
Bellan, Leon M.
Lippmann, Ethan S.
Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells
title Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells
title_full Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells
title_fullStr Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells
title_full_unstemmed Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells
title_short Modeling Neurovascular Disorders and Therapeutic Outcomes with Human-Induced Pluripotent Stem Cells
title_sort modeling neurovascular disorders and therapeutic outcomes with human-induced pluripotent stem cells
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797533/
https://www.ncbi.nlm.nih.gov/pubmed/29441348
http://dx.doi.org/10.3389/fbioe.2017.00087
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