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A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity

Here we demonstrate a facile method by which to deliver complex spatiotemporal stimulation to neural networks in fast patterns, to trigger interesting forms of circuit-level plasticity in cortical areas. We present a complete platform by which patterns of electricity can be arbitrarily defined and d...

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Detalles Bibliográficos
Autores principales: Wilson, Nathan R., Wang, Forea L., Chen, Naiyan, Yan, Sherry X., Daitch, Amy L., Shi, Bo, Sharma, Samvaran, Sur, Mriganka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766665/
https://www.ncbi.nlm.nih.gov/pubmed/35069127
http://dx.doi.org/10.3389/fncir.2021.792228
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author Wilson, Nathan R.
Wang, Forea L.
Chen, Naiyan
Yan, Sherry X.
Daitch, Amy L.
Shi, Bo
Sharma, Samvaran
Sur, Mriganka
author_facet Wilson, Nathan R.
Wang, Forea L.
Chen, Naiyan
Yan, Sherry X.
Daitch, Amy L.
Shi, Bo
Sharma, Samvaran
Sur, Mriganka
author_sort Wilson, Nathan R.
collection PubMed
description Here we demonstrate a facile method by which to deliver complex spatiotemporal stimulation to neural networks in fast patterns, to trigger interesting forms of circuit-level plasticity in cortical areas. We present a complete platform by which patterns of electricity can be arbitrarily defined and distributed across a brain circuit, either simultaneously, asynchronously, or in complex patterns that can be easily designed and orchestrated with precise timing. Interfacing with acute slices of mouse cortex, we show that our system can be used to activate neurons at many locations and drive synaptic transmission in distributed patterns, and that this elicits new forms of plasticity that may not be observable via traditional methods, including interesting measurements of associational and sequence plasticity. Finally, we introduce an automated “network assay” for imaging activation and plasticity across a circuit. Spatiotemporal stimulation opens the door for high-throughput explorations of plasticity at the circuit level, and may provide a basis for new types of adaptive neural prosthetics.
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spelling pubmed-87666652022-01-20 A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity Wilson, Nathan R. Wang, Forea L. Chen, Naiyan Yan, Sherry X. Daitch, Amy L. Shi, Bo Sharma, Samvaran Sur, Mriganka Front Neural Circuits Neuroscience Here we demonstrate a facile method by which to deliver complex spatiotemporal stimulation to neural networks in fast patterns, to trigger interesting forms of circuit-level plasticity in cortical areas. We present a complete platform by which patterns of electricity can be arbitrarily defined and distributed across a brain circuit, either simultaneously, asynchronously, or in complex patterns that can be easily designed and orchestrated with precise timing. Interfacing with acute slices of mouse cortex, we show that our system can be used to activate neurons at many locations and drive synaptic transmission in distributed patterns, and that this elicits new forms of plasticity that may not be observable via traditional methods, including interesting measurements of associational and sequence plasticity. Finally, we introduce an automated “network assay” for imaging activation and plasticity across a circuit. Spatiotemporal stimulation opens the door for high-throughput explorations of plasticity at the circuit level, and may provide a basis for new types of adaptive neural prosthetics. Frontiers Media S.A. 2022-01-05 /pmc/articles/PMC8766665/ /pubmed/35069127 http://dx.doi.org/10.3389/fncir.2021.792228 Text en Copyright © 2022 Wilson, Wang, Chen, Yan, Daitch, Shi, Sharma and Sur. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Wilson, Nathan R.
Wang, Forea L.
Chen, Naiyan
Yan, Sherry X.
Daitch, Amy L.
Shi, Bo
Sharma, Samvaran
Sur, Mriganka
A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity
title A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity
title_full A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity
title_fullStr A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity
title_full_unstemmed A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity
title_short A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity
title_sort platform for spatiotemporal “matrix” stimulation in brain networks reveals novel forms of circuit plasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766665/
https://www.ncbi.nlm.nih.gov/pubmed/35069127
http://dx.doi.org/10.3389/fncir.2021.792228
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