Abstract

Neuronal physiology is particularly sensitive to acute stressors that affect excitability, many of which can trigger seizures and epilepsies. Although intrinsic neuronal homeostasis plays an important role in maintaining overall nervous system robustness and its resistance to stressors, the specific genetic and molecular mechanisms that underlie these processes are not well understood. Here we used a reverse genetic approach in Drosophila to test the hypothesis that specific voltage-gated ion channels contribute to neuronal homeostasis, robustness, and stress resistance. We found that the activity of the voltage-gated potassium channel seizure (sei), an ortholog of the mammalian ERG channel family, is essential for protecting flies from acute heat-induced seizures. Although sei is broadly expressed in the nervous system, our data indicate that its impact on the organismal robustness to acute environmental stress is primarily mediated via its action in excitatory neurons, the octopaminergic system, as well as neuropile ensheathing and perineurial glia. Furthermore, our studies suggest that human mutations in the human ERG channel (hERG), which have been primarily implicated in the cardiac Long QT Syndrome (LQTS), may also contribute to the high incidence of seizures in LQTS patients via a cardiovascular-independent neurogenic pathway.

Highlights

  • Neuronal homeostatic responses to acute and long-term environmental stressors are essential for maintaining robust behavioral outputs and overall organismal fitness [1,2,3]

  • We show that in the fruit fly, mutations in the ERG voltage-gated potassium channel seizure, an ortholog of the human human ERG channel (hERG) channel that has been previously implicated in the cardiac Long-QT syndrome, increases seizure susceptibility

  • By using a tissue-specific RNAi knockdown screen of voltage-gated potassium channels, we identified seizure, the fly ortholog of the mammalian hERG channel (KCNH2) [26, 29, 32,33,34,35], as an ERG channels are required for neuronal homeostasis essential element in the neuronal homeostatic response to acute heat stress

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Summary

Introduction

Neuronal homeostatic responses to acute and long-term environmental stressors are essential for maintaining robust behavioral outputs and overall organismal fitness [1,2,3]. Many environmental stressors, such as changes in temperature or oxygen availability, impact various aspects of neuronal system function [1]. While some of the transcriptional and physiological processes that enable neurons to adjust their intrinsic activity levels in response to long-term stressors have been identified, primarily via the altered conductance of voltage-gated ion channels [11,12,13], most of the genetic and molecular mechanisms that mediate susceptibility to acute, environmentally-induced seizures, such as fever-induced febrile seizures, remain unknown [14,15,16]

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