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Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion

Using multi-color visible lights for independent optogenetic manipulation of multiple neuronal populations offers the ability for sophisticated brain functions and behavior dissection. To mitigate invasive fiber insertion, infrared light excitable upconversion nanoparticles (UCNPs) with deep tissue...

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Autores principales: Liu, Xuan, Chen, Heming, Wang, Yiting, Si, Yueguang, Zhang, Hongxin, Li, Xiaomin, Zhang, Zhengcheng, Yan, Biao, Jiang, Su, Wang, Fei, Weng, Shijun, Xu, Wendong, Zhao, Dongyuan, Zhang, Jiayi, Zhang, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476604/
https://www.ncbi.nlm.nih.gov/pubmed/34580314
http://dx.doi.org/10.1038/s41467-021-25993-7
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author Liu, Xuan
Chen, Heming
Wang, Yiting
Si, Yueguang
Zhang, Hongxin
Li, Xiaomin
Zhang, Zhengcheng
Yan, Biao
Jiang, Su
Wang, Fei
Weng, Shijun
Xu, Wendong
Zhao, Dongyuan
Zhang, Jiayi
Zhang, Fan
author_facet Liu, Xuan
Chen, Heming
Wang, Yiting
Si, Yueguang
Zhang, Hongxin
Li, Xiaomin
Zhang, Zhengcheng
Yan, Biao
Jiang, Su
Wang, Fei
Weng, Shijun
Xu, Wendong
Zhao, Dongyuan
Zhang, Jiayi
Zhang, Fan
author_sort Liu, Xuan
collection PubMed
description Using multi-color visible lights for independent optogenetic manipulation of multiple neuronal populations offers the ability for sophisticated brain functions and behavior dissection. To mitigate invasive fiber insertion, infrared light excitable upconversion nanoparticles (UCNPs) with deep tissue penetration have been implemented in optogenetics. However, due to the chromatic crosstalk induced by the multiple emission peaks, conventional UCNPs or their mixture cannot independently activate multiple targeted neuronal populations. Here, we report NIR multi-color optogenetics by the well-designed trichromatic UCNPs with excitation-specific luminescence. The blue, green and red color emissions can be separately tuned by switching excitation wavelength to match respective spectral profiles of optogenetic proteins ChR2, C1V1 and ChrimsonR, which enables selective activation of three distinct neuronal populations. Such stimulation with tunable intensity can not only activate distinct neuronal populations selectively, but also achieve transcranial selective modulation of the motion behavior of awake-mice, which opens up a possibility of multi-color upconversion optogenetics.
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spelling pubmed-84766042021-10-22 Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion Liu, Xuan Chen, Heming Wang, Yiting Si, Yueguang Zhang, Hongxin Li, Xiaomin Zhang, Zhengcheng Yan, Biao Jiang, Su Wang, Fei Weng, Shijun Xu, Wendong Zhao, Dongyuan Zhang, Jiayi Zhang, Fan Nat Commun Article Using multi-color visible lights for independent optogenetic manipulation of multiple neuronal populations offers the ability for sophisticated brain functions and behavior dissection. To mitigate invasive fiber insertion, infrared light excitable upconversion nanoparticles (UCNPs) with deep tissue penetration have been implemented in optogenetics. However, due to the chromatic crosstalk induced by the multiple emission peaks, conventional UCNPs or their mixture cannot independently activate multiple targeted neuronal populations. Here, we report NIR multi-color optogenetics by the well-designed trichromatic UCNPs with excitation-specific luminescence. The blue, green and red color emissions can be separately tuned by switching excitation wavelength to match respective spectral profiles of optogenetic proteins ChR2, C1V1 and ChrimsonR, which enables selective activation of three distinct neuronal populations. Such stimulation with tunable intensity can not only activate distinct neuronal populations selectively, but also achieve transcranial selective modulation of the motion behavior of awake-mice, which opens up a possibility of multi-color upconversion optogenetics. Nature Publishing Group UK 2021-09-27 /pmc/articles/PMC8476604/ /pubmed/34580314 http://dx.doi.org/10.1038/s41467-021-25993-7 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
Liu, Xuan
Chen, Heming
Wang, Yiting
Si, Yueguang
Zhang, Hongxin
Li, Xiaomin
Zhang, Zhengcheng
Yan, Biao
Jiang, Su
Wang, Fei
Weng, Shijun
Xu, Wendong
Zhao, Dongyuan
Zhang, Jiayi
Zhang, Fan
Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion
title Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion
title_full Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion
title_fullStr Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion
title_full_unstemmed Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion
title_short Near-infrared manipulation of multiple neuronal populations via trichromatic upconversion
title_sort near-infrared manipulation of multiple neuronal populations via trichromatic upconversion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476604/
https://www.ncbi.nlm.nih.gov/pubmed/34580314
http://dx.doi.org/10.1038/s41467-021-25993-7
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