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Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter

Neuromodulation at high spatial resolution poses great significance in advancing fundamental knowledge in the field of neuroscience and offering novel clinical treatments. Here, we developed a tapered fiber optoacoustic emitter (TFOE) generating an ultrasound field with a high spatial precision of 3...

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Autores principales: Shi, Linli, Jiang, Ying, Fernandez, Fernando R., Chen, Guo, Lan, Lu, Man, Heng-Ye, White, John A., Cheng, Ji-Xin, Yang, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277806/
https://www.ncbi.nlm.nih.gov/pubmed/34257273
http://dx.doi.org/10.1038/s41377-021-00580-z
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author Shi, Linli
Jiang, Ying
Fernandez, Fernando R.
Chen, Guo
Lan, Lu
Man, Heng-Ye
White, John A.
Cheng, Ji-Xin
Yang, Chen
author_facet Shi, Linli
Jiang, Ying
Fernandez, Fernando R.
Chen, Guo
Lan, Lu
Man, Heng-Ye
White, John A.
Cheng, Ji-Xin
Yang, Chen
author_sort Shi, Linli
collection PubMed
description Neuromodulation at high spatial resolution poses great significance in advancing fundamental knowledge in the field of neuroscience and offering novel clinical treatments. Here, we developed a tapered fiber optoacoustic emitter (TFOE) generating an ultrasound field with a high spatial precision of 39.6 µm, enabling optoacoustic activation of single neurons or subcellular structures, such as axons and dendrites. Temporally, a single acoustic pulse of sub-microsecond converted by the TFOE from a single laser pulse of 3 ns is shown as the shortest acoustic stimuli so far for successful neuron activation. The precise ultrasound generated by the TFOE enabled the integration of the optoacoustic stimulation with highly stable patch-clamp recording on single neurons. Direct measurements of the electrical response of single neurons to acoustic stimulation, which is difficult for conventional ultrasound stimulation, have been demonstrated. By coupling TFOE with ex vivo brain slice electrophysiology, we unveil cell-type-specific responses of excitatory and inhibitory neurons to acoustic stimulation. These results demonstrate that TFOE is a non-genetic single-cell and sub-cellular modulation technology, which could shed new insights into the mechanism of ultrasound neurostimulation.
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spelling pubmed-82778062021-07-19 Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter Shi, Linli Jiang, Ying Fernandez, Fernando R. Chen, Guo Lan, Lu Man, Heng-Ye White, John A. Cheng, Ji-Xin Yang, Chen Light Sci Appl Article Neuromodulation at high spatial resolution poses great significance in advancing fundamental knowledge in the field of neuroscience and offering novel clinical treatments. Here, we developed a tapered fiber optoacoustic emitter (TFOE) generating an ultrasound field with a high spatial precision of 39.6 µm, enabling optoacoustic activation of single neurons or subcellular structures, such as axons and dendrites. Temporally, a single acoustic pulse of sub-microsecond converted by the TFOE from a single laser pulse of 3 ns is shown as the shortest acoustic stimuli so far for successful neuron activation. The precise ultrasound generated by the TFOE enabled the integration of the optoacoustic stimulation with highly stable patch-clamp recording on single neurons. Direct measurements of the electrical response of single neurons to acoustic stimulation, which is difficult for conventional ultrasound stimulation, have been demonstrated. By coupling TFOE with ex vivo brain slice electrophysiology, we unveil cell-type-specific responses of excitatory and inhibitory neurons to acoustic stimulation. These results demonstrate that TFOE is a non-genetic single-cell and sub-cellular modulation technology, which could shed new insights into the mechanism of ultrasound neurostimulation. Nature Publishing Group UK 2021-07-14 /pmc/articles/PMC8277806/ /pubmed/34257273 http://dx.doi.org/10.1038/s41377-021-00580-z Text en © The Author(s) 2021 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
Shi, Linli
Jiang, Ying
Fernandez, Fernando R.
Chen, Guo
Lan, Lu
Man, Heng-Ye
White, John A.
Cheng, Ji-Xin
Yang, Chen
Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter
title Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter
title_full Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter
title_fullStr Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter
title_full_unstemmed Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter
title_short Non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter
title_sort non-genetic photoacoustic stimulation of single neurons by a tapered fiber optoacoustic emitter
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277806/
https://www.ncbi.nlm.nih.gov/pubmed/34257273
http://dx.doi.org/10.1038/s41377-021-00580-z
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