Nuclear BK channels regulate gene expression via the control of nuclear calcium signaling

Nat Neurosci. 2014 Aug;17(8):1055-63. doi: 10.1038/nn.3744. Epub 2014 Jun 22.

Abstract

Ion channels are essential for the regulation of neuronal functions. The significance of plasma membrane, mitochondrial, endoplasmic reticulum and lysosomal ion channels in the regulation of Ca(2+) is well established. In contrast, surprisingly little is known about the function of ion channels on the nuclear envelope (NE). Here we demonstrate the presence of functional large-conductance, calcium-activated potassium channels (BK channels) on the NE of rodent hippocampal neurons. Functionally, blockade of nuclear BK channels (nBK channels) induces NE-derived Ca(2+) release, nucleoplasmic Ca(2+) elevation and cyclic AMP response element binding protein (CREB)-dependent transcription. More importantly, blockade of nBK channels regulates nuclear Ca(2+)-sensitive gene expression and promotes dendritic arborization in a nuclear Ca(2+)-dependent manner. These results suggest that the nBK channel functions as a molecular link between neuronal activity and nuclear Ca(2+) to convey signals from synapse to nucleus and is a new modulator, operating at the NE, of synaptic activity-dependent neuronal functions.

Publication types

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

MeSH terms

  • Animals
  • Calcium Signaling / genetics*
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Gene Expression Regulation*
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits / deficiency
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits / genetics*
  • Large-Conductance Calcium-Activated Potassium Channels / genetics
  • Large-Conductance Calcium-Activated Potassium Channels / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neurons / cytology
  • Neurons / metabolism
  • Nuclear Envelope / genetics*
  • Nuclear Envelope / metabolism*
  • Nuclear Envelope / ultrastructure
  • Phosphorylation / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Synaptic Transmission / genetics

Substances

  • Creb1 protein, mouse
  • Cyclic AMP Response Element-Binding Protein
  • Kcnma1 protein, mouse
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
  • Large-Conductance Calcium-Activated Potassium Channels