Frontiers in Cell and Developmental Biology (May 2022)

Förster Resonance Energy Transfer-Based Single-Cell Imaging Reveals Piezo1-Induced Ca2+ Flux Mediates Membrane Ruffling and Cell Survival

  • Heon-Su Kim,
  • Heon-Su Kim,
  • Jung-Soo Suh,
  • Yoon-Kwan Jang,
  • Sang-Hyun Ahn,
  • Gyu-Ho Choi,
  • Jin-Young Yang,
  • Gah-Hyun Lim,
  • Youngmi Jung,
  • Jie Jiang,
  • Jie Sun,
  • Myungeun Suk,
  • Yingxiao Wang,
  • Tae-Jin Kim,
  • Tae-Jin Kim,
  • Tae-Jin Kim

DOI
https://doi.org/10.3389/fcell.2022.865056
Journal volume & issue
Vol. 10

Abstract

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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 Ca2+ 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 Ca2+ influx via Piezo1 requires intact caveolin, cholesterol, and cytoskeletal support. Increased cytoplasmic Ca2+ 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 Ca2+ 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.

Keywords