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High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors
Three-dimensional (3D) organotypic models that capture native-like physiological features of tissues are being pursued as clinically predictive assays for therapeutics development. A range of these models are being developed to mimic brain morphology, physiology, and pathology of neurological diseas...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653447/ https://www.ncbi.nlm.nih.gov/pubmed/36371462 http://dx.doi.org/10.1038/s42003-022-04177-z |
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author | Kundu, Srikanya Boutin, Molly E. Strong, Caroline E. Voss, Ty Ferrer, Marc |
author_facet | Kundu, Srikanya Boutin, Molly E. Strong, Caroline E. Voss, Ty Ferrer, Marc |
author_sort | Kundu, Srikanya |
collection | PubMed |
description | Three-dimensional (3D) organotypic models that capture native-like physiological features of tissues are being pursued as clinically predictive assays for therapeutics development. A range of these models are being developed to mimic brain morphology, physiology, and pathology of neurological diseases. Biofabrication of 3D gel-based cellular systems is emerging as a versatile technology to produce spatially and cell-type tailored, physiologically complex and native-like tissue models. Here we produce 3D fibrin gel-based functional neural co-culture models with human-iPSC differentiated dopaminergic or glutamatergic neurons and astrocytes. We further introduce genetically encoded fluorescence biosensors and optogenetics activation for real time functional measurements of intracellular calcium and levels of dopamine and glutamate neurotransmitters, in a high-throughput compatible plate format. We use pharmacological perturbations to demonstrate that the drug responses of 3D gel-based neural models are like those expected from in-vivo data, and in some cases, in contrast to those observed in the equivalent 2D neural models. |
format | Online Article Text |
id | pubmed-9653447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96534472022-11-15 High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors Kundu, Srikanya Boutin, Molly E. Strong, Caroline E. Voss, Ty Ferrer, Marc Commun Biol Article Three-dimensional (3D) organotypic models that capture native-like physiological features of tissues are being pursued as clinically predictive assays for therapeutics development. A range of these models are being developed to mimic brain morphology, physiology, and pathology of neurological diseases. Biofabrication of 3D gel-based cellular systems is emerging as a versatile technology to produce spatially and cell-type tailored, physiologically complex and native-like tissue models. Here we produce 3D fibrin gel-based functional neural co-culture models with human-iPSC differentiated dopaminergic or glutamatergic neurons and astrocytes. We further introduce genetically encoded fluorescence biosensors and optogenetics activation for real time functional measurements of intracellular calcium and levels of dopamine and glutamate neurotransmitters, in a high-throughput compatible plate format. We use pharmacological perturbations to demonstrate that the drug responses of 3D gel-based neural models are like those expected from in-vivo data, and in some cases, in contrast to those observed in the equivalent 2D neural models. Nature Publishing Group UK 2022-11-12 /pmc/articles/PMC9653447/ /pubmed/36371462 http://dx.doi.org/10.1038/s42003-022-04177-z Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kundu, Srikanya Boutin, Molly E. Strong, Caroline E. Voss, Ty Ferrer, Marc High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors |
title | High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors |
title_full | High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors |
title_fullStr | High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors |
title_full_unstemmed | High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors |
title_short | High throughput 3D gel-based neural organotypic model for cellular assays using fluorescence biosensors |
title_sort | high throughput 3d gel-based neural organotypic model for cellular assays using fluorescence biosensors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653447/ https://www.ncbi.nlm.nih.gov/pubmed/36371462 http://dx.doi.org/10.1038/s42003-022-04177-z |
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