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Alcohol sedation in adult Drosophila is regulated by Cysteine proteinase-1 in cortex glia.

Kristen M LeeLaura D MathiesMike Grotewiel
Published in: Communications biology (2019)
Although numerous studies have demonstrated that neuronal mechanisms regulate alcohol-related behaviors, very few have investigated the direct role of glia in behavioral responses to alcohol. The results described here begin to fill this gap in the alcohol behavior and gliobiology fields. Since Drosophila exhibit conserved behavioral responses to alcohol and their CNS glia are similar to mammalian CNS glia, we used Drosophila to begin exploring the role of glia in alcohol behavior. We found that knockdown of Cysteine proteinase-1 (Cp1) in glia increased Drosophila alcohol sedation and that this effect was specific to cortex glia and adulthood. These data implicate Cp1 and cortex glia in alcohol-related behaviors. Cortex glia are functionally homologous to mammalian astrocytes and Cp1 is orthologous to mammalian Cathepsin L. Our studies raise the possibility that cathepsins may influence behavioral responses to alcohol in mammals via roles in astrocytes.
Keyphrases
  • alcohol consumption
  • functional connectivity
  • blood brain barrier
  • intensive care unit
  • transcription factor
  • mass spectrometry
  • mechanical ventilation
  • acute respiratory distress syndrome
  • brain injury
  • early life