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Selective control of synaptically-connected circuit elements by all-optical synapses
Understanding percepts, engrams and actions requires methods for selectively modulating synaptic communication between specific subsets of interconnected cells. Here, we develop an approach to control synaptically connected elements using bioluminescent light: Luciferase-generated light, originating...
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/PMC8752598/ https://www.ncbi.nlm.nih.gov/pubmed/35017641 http://dx.doi.org/10.1038/s42003-021-02981-7 |
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author | Prakash, Mansi Murphy, Jeremy St Laurent, Robyn Friedman, Nina Crespo, Emmanuel L. Bjorefeldt, Andreas Pal, Akash Bhagat, Yuvraj Kauer, Julie A. Shaner, Nathan C. Lipscombe, Diane Moore, Christopher I. Hochgeschwender, Ute |
author_facet | Prakash, Mansi Murphy, Jeremy St Laurent, Robyn Friedman, Nina Crespo, Emmanuel L. Bjorefeldt, Andreas Pal, Akash Bhagat, Yuvraj Kauer, Julie A. Shaner, Nathan C. Lipscombe, Diane Moore, Christopher I. Hochgeschwender, Ute |
author_sort | Prakash, Mansi |
collection | PubMed |
description | Understanding percepts, engrams and actions requires methods for selectively modulating synaptic communication between specific subsets of interconnected cells. Here, we develop an approach to control synaptically connected elements using bioluminescent light: Luciferase-generated light, originating from a presynaptic axon terminal, modulates an opsin in its postsynaptic target. Vesicular-localized luciferase is released into the synaptic cleft in response to presynaptic activity, creating a real-time Optical Synapse. Light production is under experimenter-control by introduction of the small molecule luciferin. Signal transmission across this optical synapse is temporally defined by the presence of both the luciferin and presynaptic activity. We validate synaptic Interluminescence by multi-electrode recording in cultured neurons and in mice in vivo. Interluminescence represents a powerful approach to achieve synapse-specific and activity-dependent circuit control in vivo. |
format | Online Article Text |
id | pubmed-8752598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87525982022-01-20 Selective control of synaptically-connected circuit elements by all-optical synapses Prakash, Mansi Murphy, Jeremy St Laurent, Robyn Friedman, Nina Crespo, Emmanuel L. Bjorefeldt, Andreas Pal, Akash Bhagat, Yuvraj Kauer, Julie A. Shaner, Nathan C. Lipscombe, Diane Moore, Christopher I. Hochgeschwender, Ute Commun Biol Article Understanding percepts, engrams and actions requires methods for selectively modulating synaptic communication between specific subsets of interconnected cells. Here, we develop an approach to control synaptically connected elements using bioluminescent light: Luciferase-generated light, originating from a presynaptic axon terminal, modulates an opsin in its postsynaptic target. Vesicular-localized luciferase is released into the synaptic cleft in response to presynaptic activity, creating a real-time Optical Synapse. Light production is under experimenter-control by introduction of the small molecule luciferin. Signal transmission across this optical synapse is temporally defined by the presence of both the luciferin and presynaptic activity. We validate synaptic Interluminescence by multi-electrode recording in cultured neurons and in mice in vivo. Interluminescence represents a powerful approach to achieve synapse-specific and activity-dependent circuit control in vivo. Nature Publishing Group UK 2022-01-11 /pmc/articles/PMC8752598/ /pubmed/35017641 http://dx.doi.org/10.1038/s42003-021-02981-7 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 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 Prakash, Mansi Murphy, Jeremy St Laurent, Robyn Friedman, Nina Crespo, Emmanuel L. Bjorefeldt, Andreas Pal, Akash Bhagat, Yuvraj Kauer, Julie A. Shaner, Nathan C. Lipscombe, Diane Moore, Christopher I. Hochgeschwender, Ute Selective control of synaptically-connected circuit elements by all-optical synapses |
title | Selective control of synaptically-connected circuit elements by all-optical synapses |
title_full | Selective control of synaptically-connected circuit elements by all-optical synapses |
title_fullStr | Selective control of synaptically-connected circuit elements by all-optical synapses |
title_full_unstemmed | Selective control of synaptically-connected circuit elements by all-optical synapses |
title_short | Selective control of synaptically-connected circuit elements by all-optical synapses |
title_sort | selective control of synaptically-connected circuit elements by all-optical synapses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752598/ https://www.ncbi.nlm.nih.gov/pubmed/35017641 http://dx.doi.org/10.1038/s42003-021-02981-7 |
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