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Light-sheet microscopy of network activity in 3D neuronal systems

Paulina M. Wysmolek, Filippo D. Kiessler, View ORCID ProfileKatja A. Salbaum, View ORCID ProfileElijah R. Shelton, Selina Sonntag, View ORCID ProfileFriedhelm Serwane
doi: https://doi.org/10.1101/2022.06.20.496852
Paulina M. Wysmolek
1Max Planck Institute for Medical Research, Heidelberg, Germany
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Filippo D. Kiessler
2Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany
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Katja A. Salbaum
2Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany
3Graduate School of Systemic Neuroscience (GSN), Munich, Germany
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Elijah R. Shelton
2Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany
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Selina Sonntag
2Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany
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Friedhelm Serwane
2Faculty of Physics and Center for NanoScience, Ludwig-Maximilians-Universität München, Munich, Germany
3Graduate School of Systemic Neuroscience (GSN), Munich, Germany
4Munich Cluster for Systems Neurology (SyNergy), Germany
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  • For correspondence: f.serwane@lmu.de
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Abstract

In vitro systems mimicking brain regions, such as brain organoids, are revolutionizing the field of neuroscience. However, characterization of their electrical activity has remained a challenge as this requires electrophysiological readout at millisecond timescale in 3D at single-neuron resolution. While custom-built microscopes used with genetically encoded sensors start to grant this access, a thorough 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 a simple microscope for volumetric characterization of network activity with single-neuron resolution. To provide a versatile, accessible platform to the neuroscience community, we designed a minimalistic light-sheet microscope tai-lored to computational neuroscience tools to extract calcium traces. As a proof of principle, we created a 3D connectivity map of the neuronal network by imaging its spontaneous activity. High performance, low complexity setups such as ours will empower researchers to study the formation of neuronal networks in vitro for fundamental and neurodegeneration research.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted June 21, 2022.
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Light-sheet microscopy of network activity in 3D neuronal systems
Paulina M. Wysmolek, Filippo D. Kiessler, Katja A. Salbaum, Elijah R. Shelton, Selina Sonntag, Friedhelm Serwane
bioRxiv 2022.06.20.496852; doi: https://doi.org/10.1101/2022.06.20.496852
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Light-sheet microscopy of network activity in 3D neuronal systems
Paulina M. Wysmolek, Filippo D. Kiessler, Katja A. Salbaum, Elijah R. Shelton, Selina Sonntag, Friedhelm Serwane
bioRxiv 2022.06.20.496852; doi: https://doi.org/10.1101/2022.06.20.496852

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