Membrane curvature governs the distribution of Piezo1 in live cells

Piezo1 is a bona fide mechanosensitive ion channel ubiquitously expressed in mammalian cells. The distribution of Piezo1 within a cell is essential for various biological processes including cytokinesis, cell migration, and wound healing. However, the underlying principles that guide the subcellular...

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Main Authors: Yang, Shilong, Miao, Xinwen, Arnold, Steven, Li, Boxuan, Ly, Alan T., Wang, Huan, Wang, Matthew, Guo, Xiangfu, Pathak, Medha M., Zhao, Wenting, Cox, Charles D., Shi, Zheng
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/171168
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spelling sg-ntu-dr.10356-1711682023-10-27T15:31:50Z Membrane curvature governs the distribution of Piezo1 in live cells Yang, Shilong Miao, Xinwen Arnold, Steven Li, Boxuan Ly, Alan T. Wang, Huan Wang, Matthew Guo, Xiangfu Pathak, Medha M. Zhao, Wenting Cox, Charles D. Shi, Zheng School of Chemistry, Chemical Engineering and Biotechnology Engineering::Bioengineering Mammals Cell Membrane Piezo1 is a bona fide mechanosensitive ion channel ubiquitously expressed in mammalian cells. The distribution of Piezo1 within a cell is essential for various biological processes including cytokinesis, cell migration, and wound healing. However, the underlying principles that guide the subcellular distribution of Piezo1 remain largely unexplored. Here, we demonstrate that membrane curvature serves as a key regulator of the spatial distribution of Piezo1 in the plasma membrane of living cells. Piezo1 depletes from highly curved membrane protrusions such as filopodia and enriches to nanoscale membrane invaginations. Quantification of the curvature-dependent sorting of Piezo1 directly reveals the in situ nano-geometry of the Piezo1-membrane complex. Piezo1 density on filopodia increases upon activation, independent of calcium, suggesting flattening of the channel upon opening. Consequently, the expression of Piezo1 inhibits filopodia formation, an effect that diminishes with channel activation. Ministry of Education (MOE) Published version The project is supported by the National Institute of General Medical Sciences of the National Institutes of Health (NIH) under Award Number R35GM147027 (Z.S.) and by the National Institute on Drug Abuse, the National Institute of Neurological Disorders and Stroke, and the National Institute of Mental Health of the NIH under Award Number R21DA056322 (Z.S.). H.W. is supported by the Zhou family fellowship. A.T.L. acknowledges the R01(NS10981) Diversity Supplement and NIH F31 1F31NS127594-0. M.M.P acknowledges R01NS109810. W.Z. acknowledges the funding supports from the Singapore Ministry of Education (MOE) RG95/21 and the Human Frontier Science Program Foundation RGY0088/2021. 2023-10-23T06:55:55Z 2023-10-23T06:55:55Z 2022 Journal Article Yang, S., Miao, X., Arnold, S., Li, B., Ly, A. T., Wang, H., Wang, M., Guo, X., Pathak, M. M., Zhao, W., Cox, C. D. & Shi, Z. (2022). Membrane curvature governs the distribution of Piezo1 in live cells. Nature Communications, 13(1), 7467-. https://dx.doi.org/10.1038/s41467-022-35034-6 2041-1723 https://hdl.handle.net/10356/171168 10.1038/s41467-022-35034-6 36463216 2-s2.0-85143220910 1 13 7467 en RG95/21 R21DA056322 R35GM147027 Nature Communications © The Author(s) 2022, corrected publication 2023. 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/. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Bioengineering
Mammals
Cell Membrane
spellingShingle Engineering::Bioengineering
Mammals
Cell Membrane
Yang, Shilong
Miao, Xinwen
Arnold, Steven
Li, Boxuan
Ly, Alan T.
Wang, Huan
Wang, Matthew
Guo, Xiangfu
Pathak, Medha M.
Zhao, Wenting
Cox, Charles D.
Shi, Zheng
Membrane curvature governs the distribution of Piezo1 in live cells
description Piezo1 is a bona fide mechanosensitive ion channel ubiquitously expressed in mammalian cells. The distribution of Piezo1 within a cell is essential for various biological processes including cytokinesis, cell migration, and wound healing. However, the underlying principles that guide the subcellular distribution of Piezo1 remain largely unexplored. Here, we demonstrate that membrane curvature serves as a key regulator of the spatial distribution of Piezo1 in the plasma membrane of living cells. Piezo1 depletes from highly curved membrane protrusions such as filopodia and enriches to nanoscale membrane invaginations. Quantification of the curvature-dependent sorting of Piezo1 directly reveals the in situ nano-geometry of the Piezo1-membrane complex. Piezo1 density on filopodia increases upon activation, independent of calcium, suggesting flattening of the channel upon opening. Consequently, the expression of Piezo1 inhibits filopodia formation, an effect that diminishes with channel activation.
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Yang, Shilong
Miao, Xinwen
Arnold, Steven
Li, Boxuan
Ly, Alan T.
Wang, Huan
Wang, Matthew
Guo, Xiangfu
Pathak, Medha M.
Zhao, Wenting
Cox, Charles D.
Shi, Zheng
format Article
author Yang, Shilong
Miao, Xinwen
Arnold, Steven
Li, Boxuan
Ly, Alan T.
Wang, Huan
Wang, Matthew
Guo, Xiangfu
Pathak, Medha M.
Zhao, Wenting
Cox, Charles D.
Shi, Zheng
author_sort Yang, Shilong
title Membrane curvature governs the distribution of Piezo1 in live cells
title_short Membrane curvature governs the distribution of Piezo1 in live cells
title_full Membrane curvature governs the distribution of Piezo1 in live cells
title_fullStr Membrane curvature governs the distribution of Piezo1 in live cells
title_full_unstemmed Membrane curvature governs the distribution of Piezo1 in live cells
title_sort membrane curvature governs the distribution of piezo1 in live cells
publishDate 2023
url https://hdl.handle.net/10356/171168
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