Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp
Ionic currents can be evoked by mechanical inputs applied directly at the cell-substrate interface. These ionic currents are mediated by mechanically activated ion channels, where the open probability increases with increasing mechanical input. In order to study mechanically activated ion channels d...
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doaj-5453535eab374b75b27637146204ac252020-11-25T02:28:56ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852019-03-01710.3389/fbioe.2019.00047452381Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-ClampSetareh Sianati0Setareh Sianati1Anie Kurumlian2Anie Kurumlian3Evan Bailey4Kate Poole5Kate Poole6EMBL Australia Node in Single Molecule Science, School of Medical Sciences, University of New South Wales, Sydney, NSW, AustraliaCellular and Systems Physiology, School of Medical Sciences, University of New South Wales, Sydney, NSW, AustraliaEMBL Australia Node in Single Molecule Science, School of Medical Sciences, University of New South Wales, Sydney, NSW, AustraliaCellular and Systems Physiology, School of Medical Sciences, University of New South Wales, Sydney, NSW, AustraliaCellular and Systems Physiology, School of Medical Sciences, University of New South Wales, Sydney, NSW, AustraliaEMBL Australia Node in Single Molecule Science, School of Medical Sciences, University of New South Wales, Sydney, NSW, AustraliaCellular and Systems Physiology, School of Medical Sciences, University of New South Wales, Sydney, NSW, AustraliaIonic currents can be evoked by mechanical inputs applied directly at the cell-substrate interface. These ionic currents are mediated by mechanically activated ion channels, where the open probability increases with increasing mechanical input. In order to study mechanically activated ion channels directly at the interface between cells and their environment, we have developed a technique to simultaneously monitor ion channel activity whilst stimuli are applied via displacement of cell-substrate contacts. This technique utilizes whole-cell patch-clamp electrophysiology and elastomeric pillar arrays, it is quantitative and appropriate for studying channels that respond to stimuli that are propagated to an adherent cell via the physical substrate. The mammalian channels PIEZO1, PIEZO2 have been shown to be activated by substrate deflections, using this technique. In addition, TRPV4 mediated currents can be evoked by substrate deflections, in contrast to alternate stimulation methods such as membrane stretch or cellular indentation. The deflections applied at cell-substrate points mimic the magnitude of physical stimuli that impact cells in situ.https://www.frontiersin.org/article/10.3389/fbioe.2019.00047/fullmechanically-activated ion channelscell-substrate interfaceelectrophysiologypillar arraysprotocol |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Setareh Sianati Setareh Sianati Anie Kurumlian Anie Kurumlian Evan Bailey Kate Poole Kate Poole |
spellingShingle |
Setareh Sianati Setareh Sianati Anie Kurumlian Anie Kurumlian Evan Bailey Kate Poole Kate Poole Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp Frontiers in Bioengineering and Biotechnology mechanically-activated ion channels cell-substrate interface electrophysiology pillar arrays protocol |
author_facet |
Setareh Sianati Setareh Sianati Anie Kurumlian Anie Kurumlian Evan Bailey Kate Poole Kate Poole |
author_sort |
Setareh Sianati |
title |
Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp |
title_short |
Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp |
title_full |
Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp |
title_fullStr |
Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp |
title_full_unstemmed |
Analysis of Mechanically Activated Ion Channels at the Cell-Substrate Interface: Combining Pillar Arrays and Whole-Cell Patch-Clamp |
title_sort |
analysis of mechanically activated ion channels at the cell-substrate interface: combining pillar arrays and whole-cell patch-clamp |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Bioengineering and Biotechnology |
issn |
2296-4185 |
publishDate |
2019-03-01 |
description |
Ionic currents can be evoked by mechanical inputs applied directly at the cell-substrate interface. These ionic currents are mediated by mechanically activated ion channels, where the open probability increases with increasing mechanical input. In order to study mechanically activated ion channels directly at the interface between cells and their environment, we have developed a technique to simultaneously monitor ion channel activity whilst stimuli are applied via displacement of cell-substrate contacts. This technique utilizes whole-cell patch-clamp electrophysiology and elastomeric pillar arrays, it is quantitative and appropriate for studying channels that respond to stimuli that are propagated to an adherent cell via the physical substrate. The mammalian channels PIEZO1, PIEZO2 have been shown to be activated by substrate deflections, using this technique. In addition, TRPV4 mediated currents can be evoked by substrate deflections, in contrast to alternate stimulation methods such as membrane stretch or cellular indentation. The deflections applied at cell-substrate points mimic the magnitude of physical stimuli that impact cells in situ. |
topic |
mechanically-activated ion channels cell-substrate interface electrophysiology pillar arrays protocol |
url |
https://www.frontiersin.org/article/10.3389/fbioe.2019.00047/full |
work_keys_str_mv |
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