Alcohol Regulates BK Surface Expression via Wnt/β-Catenin Signaling

J Neurosci. 2016 Oct 12;36(41):10625-10639. doi: 10.1523/JNEUROSCI.0491-16.2016.

Abstract

It has been suggested that drug tolerance represents a form of learning and memory, but this has not been experimentally established at the molecular level. We show that a component of alcohol molecular tolerance (channel internalization) from rat hippocampal neurons requires protein synthesis, in common with other forms of learning and memory. We identify β-catenin as a primary necessary protein. Alcohol increases β-catenin, and blocking accumulation of β-catenin blocks alcohol-induced internalization in these neurons. In transfected HEK293 cells, suppression of Wnt/β-catenin signaling blocks ethanol-induced internalization. Conversely, activation of Wnt/β-catenin reduces BK current density. A point mutation in a putative glycogen synthase kinase phosophorylation site within the S10 region of BK blocks internalization, suggesting that Wnt/β-catenin directly regulates alcohol-induced BK internalization via glycogen synthase kinase phosphorylation. These findings establish de novo protein synthesis and Wnt/β-catenin signaling as critical in mediating a persistent form of BK molecular alcohol tolerance establishing a commonality with other forms of long-term plasticity.

Significance statement: Alcohol tolerance is a key step toward escalating alcohol consumption and subsequent dependence. Our research aims to make significant contributions toward novel, therapeutic approaches to prevent and treat alcohol misuse by understanding the molecular mechanisms of alcohol tolerance. In our current study, we identify the role of a key regulatory pathway in alcohol-induced persistent molecular changes within the hippocampus. The canonical Wnt/β-catenin pathway regulates BK channel surface expression in a protein synthesis-dependent manner reminiscent of other forms of long-term hippocampal neuronal adaptations. This unique insight opens the possibility of using clinically tested drugs, targeting the Wnt/β-catenin pathway, for the novel use of preventing and treating alcohol dependency.

Keywords: BK; EtOH; Wnt; beta-catenin; downregulation; tolerance.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Central Nervous System Depressants / pharmacology*
  • Drug Tolerance
  • Ethanol / pharmacology*
  • Glycogen Synthase Kinases / genetics
  • Glycogen Synthase Kinases / metabolism
  • HEK293 Cells
  • Humans
  • Large-Conductance Calcium-Activated Potassium Channels / biosynthesis*
  • Large-Conductance Calcium-Activated Potassium Channels / drug effects
  • Neuronal Plasticity
  • Neurons / drug effects
  • Phosphorylation
  • Point Mutation
  • Rats
  • Wnt Signaling Pathway / drug effects*
  • beta Catenin / drug effects*
  • beta Catenin / metabolism

Substances

  • Central Nervous System Depressants
  • Large-Conductance Calcium-Activated Potassium Channels
  • beta Catenin
  • Ethanol
  • Glycogen Synthase Kinases