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Lionetti, V.

Publications and source records attributed to Lionetti, V..

2 recordsLinked to original sources

Neural stimulation hardware for the selective intrafascicular modulation of the vagus nerve

The neural stimulation of the vagus nerve is able to modulate various functions of the parasympathetic response in different organs. The stimulation of the vagus nerve is a promising approach to treating inflammatory diseases, obesity, diabetes, heart failure, and hypertension. The complexity of the vagus nerve requires highly selective stimulation, allowing the modulation of target-specific organs without side effects. Here, we address this issue by adapting a neural stimulator and developing an intraneural electrode for the particular modulation of the vagus nerve. The neurostimulator parameters such as amplitude, pulse width, and pulse shape were modulated. Single-, and multi-channel stimulation was performed at different amplitudes. For the first time, I polyimide thin-film neural electrode was designed for the specific stimulation of the vagus nerve. In vivo experiments were performed in the adult minipig to validate to elicit electrically evoked action potentials and to modulate physiological functions selectively, validating the selectivity of intraneural stimulation. Electrochemical tests of the electrode and the neurostimulator showed that the stimulation hardware was working correctly. Stimulating the porcine vagus nerve resulted in selective modulation of the vagus nerve. Alpha, beta, and theta waves could be distinguished during single- and multi-channel stimulation. We have shown that the here presented system is able to activate the vagus nerve selectively and can therefore modulate the heart rate, diastolic pressure, and systolic pressure. The here presented system may be used to restore the cardiac loop after denervation by implementing biomimetic stimulation patterns. Presented methods may be used to develop intraneural electrodes adapted for various applications.

bioengineering↗

Subtilases turn on Pectin Methylesterase activity for a robust apoplastic immunity against pathogens

Plants involve a fine modulation of pectin methylesterase (PME) activity against microbes. PME activity can promote the cell wall stiffening and the production of damage signals able to induce defense responses. However, to date, the knowledge about the molecular mechanisms triggering PME activity during disease remains largely unknown. In this study, we explored the role of subtilases (SBTs), serine proteases consisting of 56 isoforms in Arabidopsis thaliana, as activators of PME activity in plant immunity. By using biochemical and reverse genetic approaches, we found that SBT3.3 and SBT3.5 are required to control PME activity and resistance to the fungus Botrytis cinerea. Arabidopsis sbt3.3 and sbt3.5 knockout mutants showed a reduced induction of PME activity and an increased susceptibility to B. cinerea. SBT3.3 expression is controlled by the damage-associated molecular patterns Oligogalacturonides. The SBT3.3 overexpression overactivates PME activity, but only during fungal infection, resulting in an increased expression of the defense-related genes and in an enhanced resistance to B. cinerea. We revealed that SBT3.3 and the Pro-PME17 isoforms are both secreted in the cell wall exploiting distinct protein secretion pathways and a different kinetic. Our findings point to SBTs as a mechanism to switch on PME activity and the related pectin integrity signaling to strengthen plant immunity against pests, in a timely manner to avoid the growth-defense trade-off. One sentence SummarySubtilases arm pectin methylesterase activity against pathogens to switch on pectin integrity signalling, reinforcing plant immunity and avoiding the growth-defense trade-offs

plant biology↗