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Fiberless multicolor neural optoelectrode for in vivo circuit analysis
Maximizing the potential of optogenetic approaches in deep brain structures of intact animals requires optical manipulation of neurons at high spatial and temporal resolutions, while simultaneously recording electrical data from those neurons. Here, we present the first fiber-less optoelectrode with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971539/ https://www.ncbi.nlm.nih.gov/pubmed/27485264 http://dx.doi.org/10.1038/srep30961 |
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author | Kampasi, Komal Stark, Eran Seymour, John Na, Kyounghwan Winful, Herbert G. Buzsáki, György Wise, Kensall D. Yoon, Euisik |
author_facet | Kampasi, Komal Stark, Eran Seymour, John Na, Kyounghwan Winful, Herbert G. Buzsáki, György Wise, Kensall D. Yoon, Euisik |
author_sort | Kampasi, Komal |
collection | PubMed |
description | Maximizing the potential of optogenetic approaches in deep brain structures of intact animals requires optical manipulation of neurons at high spatial and temporal resolutions, while simultaneously recording electrical data from those neurons. Here, we present the first fiber-less optoelectrode with a monolithically integrated optical waveguide mixer that can deliver multicolor light at a common waveguide port to achieve multicolor modulation of the same neuronal population in vivo. We demonstrate successful device implementation by achieving efficient coupling between a side-emitting injection laser diode (ILD) and a dielectric optical waveguide mixer via a gradient-index (GRIN) lens. The use of GRIN lenses attains several design features, including high optical coupling and thermal isolation between ILDs and waveguides. We validated the packaged devices in the intact brain of anesthetized mice co-expressing Channelrhodopsin-2 and Archaerhodopsin in pyramidal cells in the hippocampal CA1 region, achieving high quality recording, activation and silencing of the exact same neurons in a given local region. This fully-integrated approach demonstrates the spatial precision and scalability needed to enable independent activation and silencing of the same or different groups of neurons in dense brain regions while simultaneously recording from them, thus considerably advancing the capabilities of currently available optogenetic toolsets. |
format | Online Article Text |
id | pubmed-4971539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49715392016-08-11 Fiberless multicolor neural optoelectrode for in vivo circuit analysis Kampasi, Komal Stark, Eran Seymour, John Na, Kyounghwan Winful, Herbert G. Buzsáki, György Wise, Kensall D. Yoon, Euisik Sci Rep Article Maximizing the potential of optogenetic approaches in deep brain structures of intact animals requires optical manipulation of neurons at high spatial and temporal resolutions, while simultaneously recording electrical data from those neurons. Here, we present the first fiber-less optoelectrode with a monolithically integrated optical waveguide mixer that can deliver multicolor light at a common waveguide port to achieve multicolor modulation of the same neuronal population in vivo. We demonstrate successful device implementation by achieving efficient coupling between a side-emitting injection laser diode (ILD) and a dielectric optical waveguide mixer via a gradient-index (GRIN) lens. The use of GRIN lenses attains several design features, including high optical coupling and thermal isolation between ILDs and waveguides. We validated the packaged devices in the intact brain of anesthetized mice co-expressing Channelrhodopsin-2 and Archaerhodopsin in pyramidal cells in the hippocampal CA1 region, achieving high quality recording, activation and silencing of the exact same neurons in a given local region. This fully-integrated approach demonstrates the spatial precision and scalability needed to enable independent activation and silencing of the same or different groups of neurons in dense brain regions while simultaneously recording from them, thus considerably advancing the capabilities of currently available optogenetic toolsets. Nature Publishing Group 2016-08-03 /pmc/articles/PMC4971539/ /pubmed/27485264 http://dx.doi.org/10.1038/srep30961 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kampasi, Komal Stark, Eran Seymour, John Na, Kyounghwan Winful, Herbert G. Buzsáki, György Wise, Kensall D. Yoon, Euisik Fiberless multicolor neural optoelectrode for in vivo circuit analysis |
title | Fiberless multicolor neural optoelectrode for in vivo circuit analysis |
title_full | Fiberless multicolor neural optoelectrode for in vivo circuit analysis |
title_fullStr | Fiberless multicolor neural optoelectrode for in vivo circuit analysis |
title_full_unstemmed | Fiberless multicolor neural optoelectrode for in vivo circuit analysis |
title_short | Fiberless multicolor neural optoelectrode for in vivo circuit analysis |
title_sort | fiberless multicolor neural optoelectrode for in vivo circuit analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971539/ https://www.ncbi.nlm.nih.gov/pubmed/27485264 http://dx.doi.org/10.1038/srep30961 |
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