Yaganoglu, S;
Kalyviotis, K;
Vagena-Pantoula, C;
Jülich, D;
Gaub, BM;
Welling, M;
Lopes, T;
Lachowski, D;
Tang, SS;
Del Rio Hernandez, A;
et al.
Yaganoglu, S; Kalyviotis, K; Vagena-Pantoula, C; Jülich, D; Gaub, BM; Welling, M; Lopes, T; Lachowski, D; Tang, SS; Del Rio Hernandez, A; Salem, V; Müller, DJ; Holley, SA; Vermot, J; Shi, J; Helassa, N; Török, K; Pantazis, P
(2023)
Highly specific and non-invasive imaging of Piezo1-dependent activity across scales using GenEPi.
Nat Commun, 14 (1).
p. 4352.
ISSN 2041-1723
https://doi.org/10.1038/s41467-023-40134-y
SGUL Authors: Torok, Katalin
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Abstract
Mechanosensing is a ubiquitous process to translate external mechanical stimuli into biological responses. Piezo1 ion channels are directly gated by mechanical forces and play an essential role in cellular mechanotransduction. However, readouts of Piezo1 activity are mainly examined by invasive or indirect techniques, such as electrophysiological analyses and cytosolic calcium imaging. Here, we introduce GenEPi, a genetically-encoded fluorescent reporter for non-invasive optical monitoring of Piezo1-dependent activity. We demonstrate that GenEPi has high spatiotemporal resolution for Piezo1-dependent stimuli from the single-cell level to that of the entire organism. GenEPi reveals transient, local mechanical stimuli in the plasma membrane of single cells, resolves repetitive contraction-triggered stimulation of beating cardiomyocytes within microtissues, and allows for robust and reliable monitoring of Piezo1-dependent activity in vivo. GenEPi will enable non-invasive optical monitoring of Piezo1 activity in mechanochemical feedback loops during development, homeostatic regulation, and disease.
Item Type: | Article | ||||||||||||||||||||||||||||||
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Additional Information: | Correction available at https://doi.org/10.1038/s41467-023-41606-x 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/. © The Author(s) 2023, corrected publication 2023 | ||||||||||||||||||||||||||||||
Keywords: | Mechanotransduction, Cellular, Ion Channels, Cell Membrane, Mechanical Phenomena, Cell Membrane, Ion Channels, Mechanotransduction, Cellular, Mechanical Phenomena | ||||||||||||||||||||||||||||||
SGUL Research Institute / Research Centre: | Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) | ||||||||||||||||||||||||||||||
Journal or Publication Title: | Nat Commun | ||||||||||||||||||||||||||||||
ISSN: | 2041-1723 | ||||||||||||||||||||||||||||||
Language: | eng | ||||||||||||||||||||||||||||||
Dates: |
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Publisher License: | Creative Commons: Attribution 4.0 | ||||||||||||||||||||||||||||||
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PubMed ID: | 37468521 | ||||||||||||||||||||||||||||||
Web of Science ID: | WOS:001037980500032 | ||||||||||||||||||||||||||||||
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URI: | https://openaccess.sgul.ac.uk/id/eprint/115559 | ||||||||||||||||||||||||||||||
Publisher's version: | https://doi.org/10.1038/s41467-023-40134-y |
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