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A genetically encoded ionic-stress sensor reveals protons as a sleep driver

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Abstract Dynamic ionic changes are hallmarks of physiological and behavioral state transitions, including sleep in animals. Although biosensors for specific cellular ions are widely available, real-time monitoring of overall ionic strength in living organisms remains challenging. Here, we present a g enetically e ncoded n uclear translocation ionic s ensor (GENTIS) that enables direct visualization of ionic stress in vivo . Using GENTIS in C. elegans , we uncover rhythmic elevations in ionic strength during larval molting transitions that coincide with the lethargus sleep. Cytosolic proton ionic increase through inhibition of v-ATPase is sufficient to induce GENTIS nuclear translocation and evoke behavioral quiescence, characterized by reduced feeding and activation of sleep-active neurons. Apical membrane v-ATPases undergo disassembly during lethargus and under sleep-inducing stress conditions, leading to proton accumulation. Notably, this proton-mediated sleep is suppressed by proton buffering with ammonium. Together, these findings establish GENTIS as a powerful tool for tracking ionic strength dynamics in living organisms and support protons as a physiological driver of sleep.
Title: A genetically encoded ionic-stress sensor reveals protons as a sleep driver
Description:
Abstract Dynamic ionic changes are hallmarks of physiological and behavioral state transitions, including sleep in animals.
Although biosensors for specific cellular ions are widely available, real-time monitoring of overall ionic strength in living organisms remains challenging.
Here, we present a g enetically e ncoded n uclear translocation ionic s ensor (GENTIS) that enables direct visualization of ionic stress in vivo .
Using GENTIS in C.
elegans , we uncover rhythmic elevations in ionic strength during larval molting transitions that coincide with the lethargus sleep.
Cytosolic proton ionic increase through inhibition of v-ATPase is sufficient to induce GENTIS nuclear translocation and evoke behavioral quiescence, characterized by reduced feeding and activation of sleep-active neurons.
Apical membrane v-ATPases undergo disassembly during lethargus and under sleep-inducing stress conditions, leading to proton accumulation.
Notably, this proton-mediated sleep is suppressed by proton buffering with ammonium.
Together, these findings establish GENTIS as a powerful tool for tracking ionic strength dynamics in living organisms and support protons as a physiological driver of sleep.

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