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A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems
In vitro systems mimicking brain regions, brain organoids, are revolutionizing the neuroscience field. However, characterization of their electrical activity has remained a challenge as it requires readout at millisecond timescale in 3D at single-neuron resolution. While custom-built microscopes use...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705530/ https://www.ncbi.nlm.nih.gov/pubmed/36443413 http://dx.doi.org/10.1038/s41598-022-24350-y |
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author | Wysmolek, Paulina M. Kiessler, Filippo D. Salbaum, Katja A. Shelton, Elijah R. Sonntag, Selina M. Serwane, Friedhelm |
author_facet | Wysmolek, Paulina M. Kiessler, Filippo D. Salbaum, Katja A. Shelton, Elijah R. Sonntag, Selina M. Serwane, Friedhelm |
author_sort | Wysmolek, Paulina M. |
collection | PubMed |
description | In vitro systems mimicking brain regions, brain organoids, are revolutionizing the neuroscience field. However, characterization of their electrical activity has remained a challenge as it requires readout at millisecond timescale in 3D at single-neuron resolution. While custom-built microscopes used with genetically encoded sensors are now opening this door, a full 3D characterization of organoid neural activity has not been performed yet, limited by the combined complexity of the optical and the biological system. Here, we introduce an accessible minimalistic light-sheet microscope to the neuroscience community. Designed as an add-on to a standard inverted microscope it can be assembled within one day. In contrast to existing simplistic setups, our platform is suited to record volumetric calcium traces. We successfully extracted 4D calcium traces at high temporal resolution by using a lightweight piezo stage to allow for 5 Hz volumetric scanning combined with a processing pipeline for true 3D neuronal trace segmentation. As a proof of principle, we created a 3D connectivity map of a stem cell derived neuron spheroid by imaging its activity. Our fast, low complexity setup empowers researchers to study the formation of neuronal networks in vitro for fundamental and neurodegeneration research. |
format | Online Article Text |
id | pubmed-9705530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97055302022-11-30 A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems Wysmolek, Paulina M. Kiessler, Filippo D. Salbaum, Katja A. Shelton, Elijah R. Sonntag, Selina M. Serwane, Friedhelm Sci Rep Article In vitro systems mimicking brain regions, brain organoids, are revolutionizing the neuroscience field. However, characterization of their electrical activity has remained a challenge as it requires readout at millisecond timescale in 3D at single-neuron resolution. While custom-built microscopes used with genetically encoded sensors are now opening this door, a full 3D characterization of organoid neural activity has not been performed yet, limited by the combined complexity of the optical and the biological system. Here, we introduce an accessible minimalistic light-sheet microscope to the neuroscience community. Designed as an add-on to a standard inverted microscope it can be assembled within one day. In contrast to existing simplistic setups, our platform is suited to record volumetric calcium traces. We successfully extracted 4D calcium traces at high temporal resolution by using a lightweight piezo stage to allow for 5 Hz volumetric scanning combined with a processing pipeline for true 3D neuronal trace segmentation. As a proof of principle, we created a 3D connectivity map of a stem cell derived neuron spheroid by imaging its activity. Our fast, low complexity setup empowers researchers to study the formation of neuronal networks in vitro for fundamental and neurodegeneration research. Nature Publishing Group UK 2022-11-28 /pmc/articles/PMC9705530/ /pubmed/36443413 http://dx.doi.org/10.1038/s41598-022-24350-y Text en © The Author(s) 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wysmolek, Paulina M. Kiessler, Filippo D. Salbaum, Katja A. Shelton, Elijah R. Sonntag, Selina M. Serwane, Friedhelm A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems |
title | A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems |
title_full | A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems |
title_fullStr | A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems |
title_full_unstemmed | A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems |
title_short | A minimal-complexity light-sheet microscope maps network activity in 3D neuronal systems |
title_sort | minimal-complexity light-sheet microscope maps network activity in 3d neuronal systems |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705530/ https://www.ncbi.nlm.nih.gov/pubmed/36443413 http://dx.doi.org/10.1038/s41598-022-24350-y |
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