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Highly specific and non-invasive imaging of Piezo1-dependent activity across scales using GenEPi.

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
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:
DateEvent
19 July 2023Published
11 July 2023Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
R01 GM127876NIGMS NIH HHSUNSPECIFIED
094385/Z/10/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
FS/17/56/32925British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
BB/M02556X/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
BB/T017929/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
FS/17/2/32559British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
31003A_144048Swiss National Science Foundationhttp://dx.doi.org/10.13039/501100001711
334552Seventh Framework Programmehttp://dx.doi.org/10.13039/501100004963
ALTF 424-2016European Molecular Biology Organizationhttp://dx.doi.org/10.13039/100004410
PubMed ID: 37468521
Web of Science ID: WOS:001037980500032
Go to PubMed abstract
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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