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Sesti, V.

Publications and source records attributed to Sesti, V..

2 recordsLinked to original sources

Optical modulation of excitation-contraction coupling in human induced pluripotent stem cell-derived cardiomyocytes

Non-genetic photostimulation is a novel and rapidly growing multidisciplinary field of research that aims to induce light sensitivity in living systems by exploiting exogeneous phototransducers. Here we propose a recently synthetized intramembrane photoswitch, based on an azobenzene derivative (Ziapin2), for optical pacing of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). The light-mediated stimulation process has been studied by applying several characterization techniques to detect the effect on the cell properties. In particular, we recorded changes in membrane capacitance, in membrane potential (Vm), and modulation of intracellular Ca2+ dynamics. Finally, cell contractility was analyzed using a custom MATLAB algorithm. Photostimulation of intramembrane Ziapin2 causes a transient Vm hyperpolarization followed by a delayed depolarization and action potential firing. The observed initial electrical modulation nicely correlates with changes in Ca2+ dynamics and contraction rate. This work represents the proof of principle that Ziapin2 can modulate electrical activity and contractility in hiPSC-CMs, opening up a future development in cardiac physiology.

bioengineering↗

Membrane Targeted Azobenzene Drives Optical Modulation of Bacterial Membrane Potential

Recent studies have shown that bacterial membrane potential is dynamic and plays signalling roles. Yet, little is still known about the mechanisms of bacterial membrane potential regulation -owing in part to a scarcity of appropriate research tools. Optical modulation of bacterial membrane potential could fill this gap and provide a new approach to studying and controlling bacterial physiology and electrical signalling. Here, we show that a membrane-targeted azobenzene (Ziapin2) can be used to photo-modulate the membrane potential in cells of the Gram-positive bacterium Bacillus subtilis. We found that upon exposure to blue-green light ({lambda} = 470 nm), isomerization of Ziapin2 in the bacteria membrane induces hyperpolarisation of the potential. In order to investigate the origin of this phenomenon we examined ion-channel-deletion strains and ion channel blockers. We found that in presence of the chloride channel blocker idanyloxyacetic acid-94 (IAA-94) or in absence of KtrAB potassium transporter, the hyperpolarisation response is attenuated. These results reveal that the Ziapin2 isomerization can induce ion channel opening in the bacterial membrane, and suggest that Ziapin2 can be used for studying and controlling bacterial electrical signalling. This new optical tool can contribute to better understand microbial phenomena, such as biofilm electric signalling and antimicrobial resistance.

biophysics↗