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Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels
Ultrasound has been used to non-invasively manipulate neuronal functions in humans and other animals. However, this approach is limited as it has been challenging to target specific cells within the brain or body. Here, we identify human Transient Receptor Potential A1 (hsTRPA1) as a candidate that...
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/PMC8828769/ https://www.ncbi.nlm.nih.gov/pubmed/35140203 http://dx.doi.org/10.1038/s41467-022-28205-y |
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author | Duque, Marc Lee-Kubli, Corinne A. Tufail, Yusuf Magaram, Uri Patel, Janki Chakraborty, Ahana Mendoza Lopez, Jose Edsinger, Eric Vasan, Aditya Shiao, Rani Weiss, Connor Friend, James Chalasani, Sreekanth H. |
author_facet | Duque, Marc Lee-Kubli, Corinne A. Tufail, Yusuf Magaram, Uri Patel, Janki Chakraborty, Ahana Mendoza Lopez, Jose Edsinger, Eric Vasan, Aditya Shiao, Rani Weiss, Connor Friend, James Chalasani, Sreekanth H. |
author_sort | Duque, Marc |
collection | PubMed |
description | Ultrasound has been used to non-invasively manipulate neuronal functions in humans and other animals. However, this approach is limited as it has been challenging to target specific cells within the brain or body. Here, we identify human Transient Receptor Potential A1 (hsTRPA1) as a candidate that confers ultrasound sensitivity to mammalian cells. Ultrasound-evoked gating of hsTRPA1 specifically requires its N-terminal tip region and cholesterol interactions; and target cells with an intact actin cytoskeleton, revealing elements of the sonogenetic mechanism. Next, we use calcium imaging and electrophysiology to show that hsTRPA1 potentiates ultrasound-evoked responses in primary neurons. Furthermore, unilateral expression of hsTRPA1 in mouse layer V motor cortical neurons leads to c-fos expression and contralateral limb responses in response to ultrasound delivered through an intact skull. Collectively, we demonstrate that hsTRPA1-based sonogenetics can effectively manipulate neurons within the intact mammalian brain, a method that could be used across species. |
format | Online Article Text |
id | pubmed-8828769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88287692022-03-17 Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels Duque, Marc Lee-Kubli, Corinne A. Tufail, Yusuf Magaram, Uri Patel, Janki Chakraborty, Ahana Mendoza Lopez, Jose Edsinger, Eric Vasan, Aditya Shiao, Rani Weiss, Connor Friend, James Chalasani, Sreekanth H. Nat Commun Article Ultrasound has been used to non-invasively manipulate neuronal functions in humans and other animals. However, this approach is limited as it has been challenging to target specific cells within the brain or body. Here, we identify human Transient Receptor Potential A1 (hsTRPA1) as a candidate that confers ultrasound sensitivity to mammalian cells. Ultrasound-evoked gating of hsTRPA1 specifically requires its N-terminal tip region and cholesterol interactions; and target cells with an intact actin cytoskeleton, revealing elements of the sonogenetic mechanism. Next, we use calcium imaging and electrophysiology to show that hsTRPA1 potentiates ultrasound-evoked responses in primary neurons. Furthermore, unilateral expression of hsTRPA1 in mouse layer V motor cortical neurons leads to c-fos expression and contralateral limb responses in response to ultrasound delivered through an intact skull. Collectively, we demonstrate that hsTRPA1-based sonogenetics can effectively manipulate neurons within the intact mammalian brain, a method that could be used across species. Nature Publishing Group UK 2022-02-09 /pmc/articles/PMC8828769/ /pubmed/35140203 http://dx.doi.org/10.1038/s41467-022-28205-y Text en © The Author(s) 2022, corrected publication 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 Duque, Marc Lee-Kubli, Corinne A. Tufail, Yusuf Magaram, Uri Patel, Janki Chakraborty, Ahana Mendoza Lopez, Jose Edsinger, Eric Vasan, Aditya Shiao, Rani Weiss, Connor Friend, James Chalasani, Sreekanth H. Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels |
title | Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels |
title_full | Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels |
title_fullStr | Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels |
title_full_unstemmed | Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels |
title_short | Sonogenetic control of mammalian cells using exogenous Transient Receptor Potential A1 channels |
title_sort | sonogenetic control of mammalian cells using exogenous transient receptor potential a1 channels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828769/ https://www.ncbi.nlm.nih.gov/pubmed/35140203 http://dx.doi.org/10.1038/s41467-022-28205-y |
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