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Kalyviotis, K.

Publications and source records attributed to Kalyviotis, K..

2 recordsLinked to original sources

Fluid shear magnitude, mechanical history and actin-sensitive coupling shape Piezo1 signalling

Mechanical forces shape cell behaviour, yet how Piezo1-associated responses encode force magnitude, recent mechanical history and cytoskeletal context under repeated fluid shear remains unclear. We combined defined fluid shear stress (FSS) with GenEPi, a genetically encoded reporter of Piezo1-proximal Ca2+ entry, in engineered XLGenEPi-HEK293T monolayers to resolve mechanically evoked responses at single-cell and population scales. GenEPi responses increased with FSS magnitude but showed diminishing response gain at higher shear. Repeated submaximal FSS produced history-dependent attenuation and reduced temporal coordination, with higher FSS accelerating the early phase of attenuation. Low-dose Latrunculin A, without significantly reducing bulk F-actin abundance, converted sustained FSS-evoked signalling into a brief, decay-dominated response while largely preserving peak responses to Yoda1. These findings show that Piezo1-associated signalling is shaped over minutes by force magnitude, recent mechanical history and actin-sensitive mechanical coupling, providing a quantitative framework for understanding mechanotransduction under sustained and repeated mechanical stimulation.

biophysics↗

Hyperspectral Oblique Plane Microscopy

Spontaneous Raman imaging has emerged as powerful label-free technique for investigating the molecular composition of biological specimens. Although Raman imaging can facilitate understanding of complex biological phenomena in vivo, current imaging modalities are limited in speed and sample compatibility. Here, we introduce a single-objective light-sheet microscope, named{lambda} -OPM, which records Raman images on a timescale of minutes to milliseconds. To demonstrate its function, we use{lambda} -OPM to map and identify micro-plastic particles based on their Raman spectral characteristics. In live zebrafish embryos, we show that{lambda} -OPM can capture wound dynamics at five-minute intervals, revealing rapid changes in cellular and extracellular matrix composition in the wounded region. Finally, we use{lambda} -OPM to obtain Raman scattering maps of a zebrafish embryos beating heart at an effective 28 frames per second, recording compositional changes at different points in the cardiac cycle.

bioengineering↗