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A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish

Detection of water motion by the lateral line relies on mechanotransduction complexes at stereocilia tips. This sensory system is comprised of neuromasts, patches of hair cells with stereociliary bundles arranged with morphological mirror symmetry that are mechanically responsive to two opposing dir...

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Autores principales: Chou, Shih-Wei, Chen, Zongwei, Zhu, Shaoyuan, Davis, Robin W., Hu, Jiaqi, Liu, Li, Fernando, Carol A., Kindig, Kayla, Brown, William C., Stepanyan, Ruben, McDermott, Brian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740173/
https://www.ncbi.nlm.nih.gov/pubmed/29269857
http://dx.doi.org/10.1038/s41467-017-01604-2
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author Chou, Shih-Wei
Chen, Zongwei
Zhu, Shaoyuan
Davis, Robin W.
Hu, Jiaqi
Liu, Li
Fernando, Carol A.
Kindig, Kayla
Brown, William C.
Stepanyan, Ruben
McDermott, Brian M.
author_facet Chou, Shih-Wei
Chen, Zongwei
Zhu, Shaoyuan
Davis, Robin W.
Hu, Jiaqi
Liu, Li
Fernando, Carol A.
Kindig, Kayla
Brown, William C.
Stepanyan, Ruben
McDermott, Brian M.
author_sort Chou, Shih-Wei
collection PubMed
description Detection of water motion by the lateral line relies on mechanotransduction complexes at stereocilia tips. This sensory system is comprised of neuromasts, patches of hair cells with stereociliary bundles arranged with morphological mirror symmetry that are mechanically responsive to two opposing directions. Here, we find that transmembrane channel-like 2b (Tmc2b) is differentially required for mechanotransduction in the zebrafish lateral line. Despite similarities in neuromast hair cell morphology, three classes of these cells can be distinguished by their Tmc2b reliance. We map mechanosensitivity along the lateral line using imaging and electrophysiology to determine that a hair cell’s Tmc2b dependence is governed by neuromast topological position and hair bundle orientation. Overall, water flow is detected by molecular machinery that can vary between hair cells of different neuromasts. Moreover, hair cells within the same neuromast can break morphologic symmetry of the sensory organ at the stereocilia tips.
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spelling pubmed-57401732017-12-26 A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish Chou, Shih-Wei Chen, Zongwei Zhu, Shaoyuan Davis, Robin W. Hu, Jiaqi Liu, Li Fernando, Carol A. Kindig, Kayla Brown, William C. Stepanyan, Ruben McDermott, Brian M. Nat Commun Article Detection of water motion by the lateral line relies on mechanotransduction complexes at stereocilia tips. This sensory system is comprised of neuromasts, patches of hair cells with stereociliary bundles arranged with morphological mirror symmetry that are mechanically responsive to two opposing directions. Here, we find that transmembrane channel-like 2b (Tmc2b) is differentially required for mechanotransduction in the zebrafish lateral line. Despite similarities in neuromast hair cell morphology, three classes of these cells can be distinguished by their Tmc2b reliance. We map mechanosensitivity along the lateral line using imaging and electrophysiology to determine that a hair cell’s Tmc2b dependence is governed by neuromast topological position and hair bundle orientation. Overall, water flow is detected by molecular machinery that can vary between hair cells of different neuromasts. Moreover, hair cells within the same neuromast can break morphologic symmetry of the sensory organ at the stereocilia tips. Nature Publishing Group UK 2017-12-21 /pmc/articles/PMC5740173/ /pubmed/29269857 http://dx.doi.org/10.1038/s41467-017-01604-2 Text en © The Author(s) 2017 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/.
spellingShingle Article
Chou, Shih-Wei
Chen, Zongwei
Zhu, Shaoyuan
Davis, Robin W.
Hu, Jiaqi
Liu, Li
Fernando, Carol A.
Kindig, Kayla
Brown, William C.
Stepanyan, Ruben
McDermott, Brian M.
A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish
title A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish
title_full A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish
title_fullStr A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish
title_full_unstemmed A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish
title_short A molecular basis for water motion detection by the mechanosensory lateral line of zebrafish
title_sort molecular basis for water motion detection by the mechanosensory lateral line of zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740173/
https://www.ncbi.nlm.nih.gov/pubmed/29269857
http://dx.doi.org/10.1038/s41467-017-01604-2
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