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Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform
Development of “organ-on-a-chip” systems for neuroscience applications are lagging due in part to the structural complexity of the nervous system and limited access of human neuronal & glial cells. In addition, rates for animal models in translating to human success are significantly lower for n...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586937/ https://www.ncbi.nlm.nih.gov/pubmed/31222141 http://dx.doi.org/10.1038/s41598-019-45407-5 |
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author | Sharma, Anup D. McCoy, Laurie Jacobs, Elizabeth Willey, Hannah Behn, Jordan Q. Nguyen, Hieu Bolon, Brad Curley, J. Lowry Moore, Michael J. |
author_facet | Sharma, Anup D. McCoy, Laurie Jacobs, Elizabeth Willey, Hannah Behn, Jordan Q. Nguyen, Hieu Bolon, Brad Curley, J. Lowry Moore, Michael J. |
author_sort | Sharma, Anup D. |
collection | PubMed |
description | Development of “organ-on-a-chip” systems for neuroscience applications are lagging due in part to the structural complexity of the nervous system and limited access of human neuronal & glial cells. In addition, rates for animal models in translating to human success are significantly lower for neurodegenerative diseases. Thus, a preclinical in vitro human cell-based model capable of providing critical clinical metrics such as nerve conduction velocity and histomorphometry are necessary to improve prediction and translation of in vitro data to successful clinical trials. To answer this challenge, we present an in vitro biomimetic model of all-human peripheral nerve tissue capable of showing robust neurite outgrowth (~5 mm), myelination of hNs by primary human Schwann cells (~5%), and evaluation of nerve conduction velocity (0.13–0.28 m/sec), previously unrealized for any human cell-based in vitro system. To the best of our knowledge, this Human Nerve-on-a-chip (HNoaC) system is the first biomimetic microphysiological system of myelinated human peripheral nerve which can be used for evaluating electrophysiological and histological metrics, the gold-standard assessment techniques previously only possible with in vivo studies. |
format | Online Article Text |
id | pubmed-6586937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65869372019-06-27 Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform Sharma, Anup D. McCoy, Laurie Jacobs, Elizabeth Willey, Hannah Behn, Jordan Q. Nguyen, Hieu Bolon, Brad Curley, J. Lowry Moore, Michael J. Sci Rep Article Development of “organ-on-a-chip” systems for neuroscience applications are lagging due in part to the structural complexity of the nervous system and limited access of human neuronal & glial cells. In addition, rates for animal models in translating to human success are significantly lower for neurodegenerative diseases. Thus, a preclinical in vitro human cell-based model capable of providing critical clinical metrics such as nerve conduction velocity and histomorphometry are necessary to improve prediction and translation of in vitro data to successful clinical trials. To answer this challenge, we present an in vitro biomimetic model of all-human peripheral nerve tissue capable of showing robust neurite outgrowth (~5 mm), myelination of hNs by primary human Schwann cells (~5%), and evaluation of nerve conduction velocity (0.13–0.28 m/sec), previously unrealized for any human cell-based in vitro system. To the best of our knowledge, this Human Nerve-on-a-chip (HNoaC) system is the first biomimetic microphysiological system of myelinated human peripheral nerve which can be used for evaluating electrophysiological and histological metrics, the gold-standard assessment techniques previously only possible with in vivo studies. Nature Publishing Group UK 2019-06-20 /pmc/articles/PMC6586937/ /pubmed/31222141 http://dx.doi.org/10.1038/s41598-019-45407-5 Text en © The Author(s) 2019 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 Sharma, Anup D. McCoy, Laurie Jacobs, Elizabeth Willey, Hannah Behn, Jordan Q. Nguyen, Hieu Bolon, Brad Curley, J. Lowry Moore, Michael J. Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform |
title | Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform |
title_full | Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform |
title_fullStr | Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform |
title_full_unstemmed | Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform |
title_short | Engineering a 3D functional human peripheral nerve in vitro using the Nerve-on-a-Chip platform |
title_sort | engineering a 3d functional human peripheral nerve in vitro using the nerve-on-a-chip platform |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586937/ https://www.ncbi.nlm.nih.gov/pubmed/31222141 http://dx.doi.org/10.1038/s41598-019-45407-5 |
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