ELKIN1-dependent Ca++ flickers in melanoma cells depend on acto-myosin contractility

Abstract Melanoma cell migration is influenced by the expression of ELKIN1, an ion channel that supports mechanically-evoked currents when mechanical stimuli are applied to the cell-substrate interface, via the substrate. The deletion of ELKIN1 from melanoma cells impacts cell migration, cell invasion and cellular adaptation to changing gravitational loads. Here, we investigated whether ELKIN1 mediates calcium flickers at the cell-substrate interface as an indicator of channel activity, in the absence of externally applied forces. We found that calcium flickers can be detected in WM266/4 melanoma cells and that these flickers largely depended on ELKIN1 expression and acto-myosin contractility. Residual calcium flicker activity was detected in cells lacking ELKIN1, that was found to depend, in part, on TRPV4. However, this activity was not further blocked by inhibition of cellular contractility. These data suggest that ELKIN1 dependent signalling can be initiated by mechanical cues arising from cellular contractility.

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Publication Details

Journal
npj Biological Physics and Mechanics.
Published
2026-10-30
DOI
https://doi.org/10.1038/s44341-026-00051-9
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

ELKIN1-dependent Ca++ flickers in melanoma cells depend on acto-myosin contractility

Lioba Schroeter, Amrutha Patkunarajah, Renee Megan Whan, Elvis Pandžić et al.
1 links
npj Biological Physics and Mechanics.
Cellular Mechanics and Interactions
article

ELKIN1-dependent Ca++ flickers in melanoma cells depend on acto-myosin contractility

Lioba Schroeter, Amrutha Patkunarajah, Renee Megan Whan, Elvis Pandžić, Kate Poole, Abie Angelo Cargando, Riley Mumberson
article en

Abstract

Abstract Melanoma cell migration is influenced by the expression of ELKIN1, an ion channel that supports mechanically-evoked currents when mechanical stimuli are applied to the cell-substrate interface, via the substrate. The deletion of ELKIN1 from melanoma cells impacts cell migration, cell invasion and cellular adaptation to changing gravitational loads. Here, we investigated whether ELKIN1 mediates calcium flickers at the cell-substrate interface as an indicator of channel activity, in the absence of externally applied forces. We found that calcium flickers can be detected in WM266/4 melanoma cells and that these flickers largely depended on ELKIN1 expression and acto-myosin contractility. Residual calcium flicker activity was detected in cells lacking ELKIN1, that was found to depend, in part, on TRPV4. However, this activity was not further blocked by inhibition of cellular contractility. These data suggest that ELKIN1 dependent signalling can be initiated by mechanical cues arising from cellular contractility.

npj Biological Physics and Mechanics.Vol. 3(1)
The University of Sydney (AU), UNSW Sydney (AU), Mark Wainwright Analytical Centre (AU)
Australian Government, Analytical Center for the Government of the Russian Federation, University of New South Wales, National Health and Medical Research Council
Openalex Percentile: Top 16%
Cellular Mechanics and Interactions
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ELKIN1-dependent Ca++ flickers in melanoma cells depend on acto-myosin contractility — Lioba Schroeter, Amrutha Patkunarajah, et al. · npj Biological Physics and Mechanics. (2026) | TGRS Research Map | TGRS