Adherent cell remodeling on micropatterns is modulated by Piezo1 channels
Abstract Adherent cells utilize local environmental cues to make decisions on their growth and movement. We have previously shown that HEK293 cells grown on the fibronectin stripe patterns were elongated. Here we show that Piezo1 function is involved in cell spreading. Piezo1 expressing HEK cells pl...
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2021-03-01
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Online Access: | https://doi.org/10.1038/s41598-021-84427-y |
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doaj-6f4a2c6f55c84bee8e66b8d6b47449e32021-03-11T12:13:06ZengNature Publishing GroupScientific Reports2045-23222021-03-011111910.1038/s41598-021-84427-yAdherent cell remodeling on micropatterns is modulated by Piezo1 channelsDeekshitha Jetta0Mohammad Reza Bahrani Fard1Frederick Sachs2Katie Munechika3Susan Z. Hua4Department of Mechanical and Aerospace Engineering, University at BuffaloDepartment of Mechanical and Aerospace Engineering, University at BuffaloDepartment of Physiology and Biophysics, University at BuffaloDepartment of Biomedical Engineering, University at BuffaloDepartment of Mechanical and Aerospace Engineering, University at BuffaloAbstract Adherent cells utilize local environmental cues to make decisions on their growth and movement. We have previously shown that HEK293 cells grown on the fibronectin stripe patterns were elongated. Here we show that Piezo1 function is involved in cell spreading. Piezo1 expressing HEK cells plated on fibronectin stripes elongated, while a knockout of Piezo1 eliminated elongation. Inhibiting Piezo1 conductance using GsMTx4 or Gd3+ blocked cell spreading, but the cells grew thin tail-like extensions along the patterns. Images of GFP-tagged Piezo1 showed plaques of Piezo1 moving to the extrusion edges, co-localized with focal adhesions. Surprisingly, in non-spreading cells Piezo1 was located primarily on the nuclear envelope. Inhibiting the Rho-ROCK pathway also reversibly inhibited cell extension indicating that myosin contractility is involved. The growth of thin extrusion tails did not occur in Piezo1 knockout cells suggesting that Piezo1 may have functions besides acting as a cation channel.https://doi.org/10.1038/s41598-021-84427-y |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Deekshitha Jetta Mohammad Reza Bahrani Fard Frederick Sachs Katie Munechika Susan Z. Hua |
spellingShingle |
Deekshitha Jetta Mohammad Reza Bahrani Fard Frederick Sachs Katie Munechika Susan Z. Hua Adherent cell remodeling on micropatterns is modulated by Piezo1 channels Scientific Reports |
author_facet |
Deekshitha Jetta Mohammad Reza Bahrani Fard Frederick Sachs Katie Munechika Susan Z. Hua |
author_sort |
Deekshitha Jetta |
title |
Adherent cell remodeling on micropatterns is modulated by Piezo1 channels |
title_short |
Adherent cell remodeling on micropatterns is modulated by Piezo1 channels |
title_full |
Adherent cell remodeling on micropatterns is modulated by Piezo1 channels |
title_fullStr |
Adherent cell remodeling on micropatterns is modulated by Piezo1 channels |
title_full_unstemmed |
Adherent cell remodeling on micropatterns is modulated by Piezo1 channels |
title_sort |
adherent cell remodeling on micropatterns is modulated by piezo1 channels |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-03-01 |
description |
Abstract Adherent cells utilize local environmental cues to make decisions on their growth and movement. We have previously shown that HEK293 cells grown on the fibronectin stripe patterns were elongated. Here we show that Piezo1 function is involved in cell spreading. Piezo1 expressing HEK cells plated on fibronectin stripes elongated, while a knockout of Piezo1 eliminated elongation. Inhibiting Piezo1 conductance using GsMTx4 or Gd3+ blocked cell spreading, but the cells grew thin tail-like extensions along the patterns. Images of GFP-tagged Piezo1 showed plaques of Piezo1 moving to the extrusion edges, co-localized with focal adhesions. Surprisingly, in non-spreading cells Piezo1 was located primarily on the nuclear envelope. Inhibiting the Rho-ROCK pathway also reversibly inhibited cell extension indicating that myosin contractility is involved. The growth of thin extrusion tails did not occur in Piezo1 knockout cells suggesting that Piezo1 may have functions besides acting as a cation channel. |
url |
https://doi.org/10.1038/s41598-021-84427-y |
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