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Adherent cell remodeling on micropatterns is modulated by Piezo1 channels

  • Deekshitha Jetta
  • , Mohammad Reza Bahrani Fard
  • , Frederick Sachs
  • , Katie Munechika
  • , Susan Z. Hua
  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

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.

Original languageEnglish
Article number5088
JournalScientific Reports
Volume11
Issue number1
DOIs
StatePublished - Dec 2021

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