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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Main Authors: Deekshitha Jetta, Mohammad Reza Bahrani Fard, Frederick Sachs, Katie Munechika, Susan Z. Hua
Format: Article
Language:English
Published: Nature Publishing Group 2021-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-84427-y
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spelling 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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