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Fast wide-volume functional imaging of engineered in vitro brain tissues
The need for in vitro models that mimic the human brain to replace animal testing and allow high-throughput screening has driven scientists to develop new tools that reproduce tissue-like features on a chip. Three-dimensional (3D) in vitro cultures are emerging as an unmatched platform that preserve...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561227/ https://www.ncbi.nlm.nih.gov/pubmed/28819205 http://dx.doi.org/10.1038/s41598-017-08979-8 |
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author | Palazzolo, G. Moroni, M. Soloperto, A. Aletti, G. Naldi, G. Vassalli, M. Nieus, T. Difato, F. |
author_facet | Palazzolo, G. Moroni, M. Soloperto, A. Aletti, G. Naldi, G. Vassalli, M. Nieus, T. Difato, F. |
author_sort | Palazzolo, G. |
collection | PubMed |
description | The need for in vitro models that mimic the human brain to replace animal testing and allow high-throughput screening has driven scientists to develop new tools that reproduce tissue-like features on a chip. Three-dimensional (3D) in vitro cultures are emerging as an unmatched platform that preserves the complexity of cell-to-cell connections within a tissue, improves cell survival, and boosts neuronal differentiation. In this context, new and flexible imaging approaches are required to monitor the functional states of 3D networks. Herein, we propose an experimental model based on 3D neuronal networks in an alginate hydrogel, a tunable wide-volume imaging approach, and an efficient denoising algorithm to resolve, down to single cell resolution, the 3D activity of hundreds of neurons expressing the calcium sensor GCaMP6s. Furthermore, we implemented a 3D co-culture system mimicking the contiguous interfaces of distinct brain tissues such as the cortical-hippocampal interface. The analysis of the network activity of single and layered neuronal co-cultures revealed cell-type-specific activities and an organization of neuronal subpopulations that changed in the two culture configurations. Overall, our experimental platform represents a simple, powerful and cost-effective platform for developing and monitoring living 3D layered brain tissue on chip structures with high resolution and high throughput. |
format | Online Article Text |
id | pubmed-5561227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55612272017-08-21 Fast wide-volume functional imaging of engineered in vitro brain tissues Palazzolo, G. Moroni, M. Soloperto, A. Aletti, G. Naldi, G. Vassalli, M. Nieus, T. Difato, F. Sci Rep Article The need for in vitro models that mimic the human brain to replace animal testing and allow high-throughput screening has driven scientists to develop new tools that reproduce tissue-like features on a chip. Three-dimensional (3D) in vitro cultures are emerging as an unmatched platform that preserves the complexity of cell-to-cell connections within a tissue, improves cell survival, and boosts neuronal differentiation. In this context, new and flexible imaging approaches are required to monitor the functional states of 3D networks. Herein, we propose an experimental model based on 3D neuronal networks in an alginate hydrogel, a tunable wide-volume imaging approach, and an efficient denoising algorithm to resolve, down to single cell resolution, the 3D activity of hundreds of neurons expressing the calcium sensor GCaMP6s. Furthermore, we implemented a 3D co-culture system mimicking the contiguous interfaces of distinct brain tissues such as the cortical-hippocampal interface. The analysis of the network activity of single and layered neuronal co-cultures revealed cell-type-specific activities and an organization of neuronal subpopulations that changed in the two culture configurations. Overall, our experimental platform represents a simple, powerful and cost-effective platform for developing and monitoring living 3D layered brain tissue on chip structures with high resolution and high throughput. Nature Publishing Group UK 2017-08-17 /pmc/articles/PMC5561227/ /pubmed/28819205 http://dx.doi.org/10.1038/s41598-017-08979-8 Text en © The Author(s) 2017 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 Palazzolo, G. Moroni, M. Soloperto, A. Aletti, G. Naldi, G. Vassalli, M. Nieus, T. Difato, F. Fast wide-volume functional imaging of engineered in vitro brain tissues |
title | Fast wide-volume functional imaging of engineered in vitro brain tissues |
title_full | Fast wide-volume functional imaging of engineered in vitro brain tissues |
title_fullStr | Fast wide-volume functional imaging of engineered in vitro brain tissues |
title_full_unstemmed | Fast wide-volume functional imaging of engineered in vitro brain tissues |
title_short | Fast wide-volume functional imaging of engineered in vitro brain tissues |
title_sort | fast wide-volume functional imaging of engineered in vitro brain tissues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561227/ https://www.ncbi.nlm.nih.gov/pubmed/28819205 http://dx.doi.org/10.1038/s41598-017-08979-8 |
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