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Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling

The integral selectivity characteristic of the blood brain barrier (BBB) limits therapeutic options for many neurologic diseases and disorders. Currently, very little is known about the mechanisms that govern the dynamic nature of the BBB. Recent reports have focused on the development and applicati...

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Autores principales: Nzou, Goodwell, Wicks, R. T., Wicks, E. E., Seale, S. A., Sane, C. H., Chen, A., Murphy, S. V., Jackson, J. D., Atala, A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943588/
https://www.ncbi.nlm.nih.gov/pubmed/29743549
http://dx.doi.org/10.1038/s41598-018-25603-5
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author Nzou, Goodwell
Wicks, R. T.
Wicks, E. E.
Seale, S. A.
Sane, C. H.
Chen, A.
Murphy, S. V.
Jackson, J. D.
Atala, A. J.
author_facet Nzou, Goodwell
Wicks, R. T.
Wicks, E. E.
Seale, S. A.
Sane, C. H.
Chen, A.
Murphy, S. V.
Jackson, J. D.
Atala, A. J.
author_sort Nzou, Goodwell
collection PubMed
description The integral selectivity characteristic of the blood brain barrier (BBB) limits therapeutic options for many neurologic diseases and disorders. Currently, very little is known about the mechanisms that govern the dynamic nature of the BBB. Recent reports have focused on the development and application of human brain organoids developed from neuro-progenitor cells. While these models provide an excellent platform to study the effects of disease and genetic aberrances on brain development, they may not model the microvasculature and BBB of the adult human cortex. To date, most in vitro BBB models utilize endothelial cells, pericytes and astrocytes. We report a 3D spheroid model of the BBB comprising all major cell types, including neurons, microglia and oligodendrocytes, to recapitulate more closely normal human brain tissue. Spheroids show expression of tight junctions, adherens junctions, adherens junction-associated proteins and cell specific markers. Functional assessment using MPTP, MPP+ and mercury chloride indicate charge selectivity through the barrier. Junctional protein distribution was altered under hypoxic conditions. Our spheroid model may have potential applications in drug discovery, disease modeling, neurotoxicity and cytotoxicity testing.
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spelling pubmed-59435882018-05-14 Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling Nzou, Goodwell Wicks, R. T. Wicks, E. E. Seale, S. A. Sane, C. H. Chen, A. Murphy, S. V. Jackson, J. D. Atala, A. J. Sci Rep Article The integral selectivity characteristic of the blood brain barrier (BBB) limits therapeutic options for many neurologic diseases and disorders. Currently, very little is known about the mechanisms that govern the dynamic nature of the BBB. Recent reports have focused on the development and application of human brain organoids developed from neuro-progenitor cells. While these models provide an excellent platform to study the effects of disease and genetic aberrances on brain development, they may not model the microvasculature and BBB of the adult human cortex. To date, most in vitro BBB models utilize endothelial cells, pericytes and astrocytes. We report a 3D spheroid model of the BBB comprising all major cell types, including neurons, microglia and oligodendrocytes, to recapitulate more closely normal human brain tissue. Spheroids show expression of tight junctions, adherens junctions, adherens junction-associated proteins and cell specific markers. Functional assessment using MPTP, MPP+ and mercury chloride indicate charge selectivity through the barrier. Junctional protein distribution was altered under hypoxic conditions. Our spheroid model may have potential applications in drug discovery, disease modeling, neurotoxicity and cytotoxicity testing. Nature Publishing Group UK 2018-05-09 /pmc/articles/PMC5943588/ /pubmed/29743549 http://dx.doi.org/10.1038/s41598-018-25603-5 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nzou, Goodwell
Wicks, R. T.
Wicks, E. E.
Seale, S. A.
Sane, C. H.
Chen, A.
Murphy, S. V.
Jackson, J. D.
Atala, A. J.
Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling
title Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling
title_full Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling
title_fullStr Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling
title_full_unstemmed Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling
title_short Human Cortex Spheroid with a Functional Blood Brain Barrier for High-Throughput Neurotoxicity Screening and Disease Modeling
title_sort human cortex spheroid with a functional blood brain barrier for high-throughput neurotoxicity screening and disease modeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943588/
https://www.ncbi.nlm.nih.gov/pubmed/29743549
http://dx.doi.org/10.1038/s41598-018-25603-5
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