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Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival

A mechanosensitive ion channel, Piezo1 induces non-selective cation flux in response to various mechanical stresses. However, the biological interpretation and underlying mechanisms of cells resulting from Piezo1 activation remain elusive. This study elucidates Piezo1-mediated Ca(2+) influx driven b...

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Autores principales: Kim, Heon-Su, Suh, Jung-Soo, Jang, Yoon-Kwan, Ahn, Sang-Hyun, Choi, Gyu-Ho, Yang, Jin-Young, Lim, Gah-Hyun, Jung, Youngmi, Jiang, Jie, Sun, Jie, Suk, Myungeun, Wang, Yingxiao, Kim, Tae-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136143/
https://www.ncbi.nlm.nih.gov/pubmed/35646889
http://dx.doi.org/10.3389/fcell.2022.865056
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author Kim, Heon-Su
Suh, Jung-Soo
Jang, Yoon-Kwan
Ahn, Sang-Hyun
Choi, Gyu-Ho
Yang, Jin-Young
Lim, Gah-Hyun
Jung, Youngmi
Jiang, Jie
Sun, Jie
Suk, Myungeun
Wang, Yingxiao
Kim, Tae-Jin
author_facet Kim, Heon-Su
Suh, Jung-Soo
Jang, Yoon-Kwan
Ahn, Sang-Hyun
Choi, Gyu-Ho
Yang, Jin-Young
Lim, Gah-Hyun
Jung, Youngmi
Jiang, Jie
Sun, Jie
Suk, Myungeun
Wang, Yingxiao
Kim, Tae-Jin
author_sort Kim, Heon-Su
collection PubMed
description A mechanosensitive ion channel, Piezo1 induces non-selective cation flux in response to various mechanical stresses. However, the biological interpretation and underlying mechanisms of cells resulting from Piezo1 activation remain elusive. This study elucidates Piezo1-mediated Ca(2+) influx driven by channel activation and cellular behavior using novel Förster Resonance Energy Transfer (FRET)-based biosensors and single-cell imaging analysis. Results reveal that extracellular Ca(2+) influx via Piezo1 requires intact caveolin, cholesterol, and cytoskeletal support. Increased cytoplasmic Ca(2+) levels enhance PKA, ERK, Rac1, and ROCK activity, which have the potential to promote cancer cell survival and migration. Furthermore, we demonstrate that Piezo1-mediated Ca(2+) influx upregulates membrane ruffling, a characteristic feature of cancer cell metastasis, using spatiotemporal image correlation spectroscopy. Thus, our findings provide new insights into the function of Piezo1, suggesting that Piezo1 plays a significant role in the behavior of cancer cells.
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spelling pubmed-91361432022-05-28 Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival Kim, Heon-Su Suh, Jung-Soo Jang, Yoon-Kwan Ahn, Sang-Hyun Choi, Gyu-Ho Yang, Jin-Young Lim, Gah-Hyun Jung, Youngmi Jiang, Jie Sun, Jie Suk, Myungeun Wang, Yingxiao Kim, Tae-Jin Front Cell Dev Biol Cell and Developmental Biology A mechanosensitive ion channel, Piezo1 induces non-selective cation flux in response to various mechanical stresses. However, the biological interpretation and underlying mechanisms of cells resulting from Piezo1 activation remain elusive. This study elucidates Piezo1-mediated Ca(2+) influx driven by channel activation and cellular behavior using novel Förster Resonance Energy Transfer (FRET)-based biosensors and single-cell imaging analysis. Results reveal that extracellular Ca(2+) influx via Piezo1 requires intact caveolin, cholesterol, and cytoskeletal support. Increased cytoplasmic Ca(2+) levels enhance PKA, ERK, Rac1, and ROCK activity, which have the potential to promote cancer cell survival and migration. Furthermore, we demonstrate that Piezo1-mediated Ca(2+) influx upregulates membrane ruffling, a characteristic feature of cancer cell metastasis, using spatiotemporal image correlation spectroscopy. Thus, our findings provide new insights into the function of Piezo1, suggesting that Piezo1 plays a significant role in the behavior of cancer cells. Frontiers Media S.A. 2022-05-13 /pmc/articles/PMC9136143/ /pubmed/35646889 http://dx.doi.org/10.3389/fcell.2022.865056 Text en Copyright © 2022 Kim, Suh, Jang, Ahn, Choi, Yang, Lim, Jung, Jiang, Sun, Suk, Wang and Kim. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Kim, Heon-Su
Suh, Jung-Soo
Jang, Yoon-Kwan
Ahn, Sang-Hyun
Choi, Gyu-Ho
Yang, Jin-Young
Lim, Gah-Hyun
Jung, Youngmi
Jiang, Jie
Sun, Jie
Suk, Myungeun
Wang, Yingxiao
Kim, Tae-Jin
Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival
title Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival
title_full Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival
title_fullStr Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival
title_full_unstemmed Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival
title_short Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca(2+) Flux Mediates Membrane Ruffling and Cell Survival
title_sort förster resonance energy transfer-based single-cell imaging reveals piezo1-induced ca(2+) flux mediates membrane ruffling and cell survival
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136143/
https://www.ncbi.nlm.nih.gov/pubmed/35646889
http://dx.doi.org/10.3389/fcell.2022.865056
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