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A directional 3D neurite outgrowth model for studying motor axon biology and disease
We report a method to generate a 3D motor neuron model with segregated and directed axonal outgrowth. iPSC-derived motor neurons are cultured in extracellular matrix gel in a microfluidic platform. Neurons extend their axons into an adjacent layer of gel, whereas dendrites and soma remain predominan...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822896/ https://www.ncbi.nlm.nih.gov/pubmed/33483540 http://dx.doi.org/10.1038/s41598-021-81335-z |
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author | Spijkers, Xandor M. Pasteuning-Vuhman, Svetlana Dorleijn, Jennifa C. Vulto, Paul Wevers, Nienke R. Pasterkamp, R. Jeroen |
author_facet | Spijkers, Xandor M. Pasteuning-Vuhman, Svetlana Dorleijn, Jennifa C. Vulto, Paul Wevers, Nienke R. Pasterkamp, R. Jeroen |
author_sort | Spijkers, Xandor M. |
collection | PubMed |
description | We report a method to generate a 3D motor neuron model with segregated and directed axonal outgrowth. iPSC-derived motor neurons are cultured in extracellular matrix gel in a microfluidic platform. Neurons extend their axons into an adjacent layer of gel, whereas dendrites and soma remain predominantly in the somal compartment, as verified by immunofluorescent staining. Axonal outgrowth could be precisely quantified and was shown to respond to the chemotherapeutic drug vincristine in a highly reproducible dose-dependent manner. The model was shown susceptible to excitotoxicity upon exposure with excess glutamate and showed formation of stress granules upon excess glutamate or sodium arsenite exposure, mimicking processes common in motor neuron diseases. Importantly, outgrowing axons could be attracted and repelled through a gradient of axonal guidance cues, such as semaphorins. The platform comprises 40 chips arranged underneath a microtiter plate providing both throughput and compatibility to standard laboratory equipment. The model will thus prove ideal for studying axonal biology and disease, drug discovery and regenerative medicine. |
format | Online Article Text |
id | pubmed-7822896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78228962021-01-26 A directional 3D neurite outgrowth model for studying motor axon biology and disease Spijkers, Xandor M. Pasteuning-Vuhman, Svetlana Dorleijn, Jennifa C. Vulto, Paul Wevers, Nienke R. Pasterkamp, R. Jeroen Sci Rep Article We report a method to generate a 3D motor neuron model with segregated and directed axonal outgrowth. iPSC-derived motor neurons are cultured in extracellular matrix gel in a microfluidic platform. Neurons extend their axons into an adjacent layer of gel, whereas dendrites and soma remain predominantly in the somal compartment, as verified by immunofluorescent staining. Axonal outgrowth could be precisely quantified and was shown to respond to the chemotherapeutic drug vincristine in a highly reproducible dose-dependent manner. The model was shown susceptible to excitotoxicity upon exposure with excess glutamate and showed formation of stress granules upon excess glutamate or sodium arsenite exposure, mimicking processes common in motor neuron diseases. Importantly, outgrowing axons could be attracted and repelled through a gradient of axonal guidance cues, such as semaphorins. The platform comprises 40 chips arranged underneath a microtiter plate providing both throughput and compatibility to standard laboratory equipment. The model will thus prove ideal for studying axonal biology and disease, drug discovery and regenerative medicine. Nature Publishing Group UK 2021-01-22 /pmc/articles/PMC7822896/ /pubmed/33483540 http://dx.doi.org/10.1038/s41598-021-81335-z Text en © The Author(s) 2021 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 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/. |
spellingShingle | Article Spijkers, Xandor M. Pasteuning-Vuhman, Svetlana Dorleijn, Jennifa C. Vulto, Paul Wevers, Nienke R. Pasterkamp, R. Jeroen A directional 3D neurite outgrowth model for studying motor axon biology and disease |
title | A directional 3D neurite outgrowth model for studying motor axon biology and disease |
title_full | A directional 3D neurite outgrowth model for studying motor axon biology and disease |
title_fullStr | A directional 3D neurite outgrowth model for studying motor axon biology and disease |
title_full_unstemmed | A directional 3D neurite outgrowth model for studying motor axon biology and disease |
title_short | A directional 3D neurite outgrowth model for studying motor axon biology and disease |
title_sort | directional 3d neurite outgrowth model for studying motor axon biology and disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822896/ https://www.ncbi.nlm.nih.gov/pubmed/33483540 http://dx.doi.org/10.1038/s41598-021-81335-z |
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