Electrophysiology and beyond: multiple roles of Na+ channel β subunits in development and disease

Neurosci Lett. 2010 Dec 10;486(2):53-9. doi: 10.1016/j.neulet.2010.06.050. Epub 2010 Jun 23.

Abstract

Voltage-gated Na+ channel (VGSC) β Subunits are not "auxiliary." These multi-functional molecules not only modulate Na+ current (I(Na)), but also function as cell adhesion molecules (CAMs)-playing roles in aggregation, migration, invasion, neurite outgrowth, and axonal fasciculation. β subunits are integral members of VGSC signaling complexes at nodes of Ranvier, axon initial segments, and cardiac intercalated disks, regulating action potential propagation through critical intermolecular and cell-cell communication events. At least in vitro, many β subunit cell adhesive functions occur both in the presence and absence of pore-forming VGSC α subunits, and in vivo β subunits are expressed in excitable as well as non-excitable cells, thus β subunits may play important functional roles on their own, in the absence of α subunits. VGSC β1 subunits are essential for life and appear to be especially important during brain development. Mutations in β subunit genes result in a variety of human neurological and cardiovascular diseases. Moreover, some cancer cells exhibit alterations in β subunit expression during metastasis. In short, these proteins, originally thought of as merely accessory to α subunits, are critical players in their own right in human health and disease. Here we discuss the role of VGSC β subunits in the nervous system.

Publication types

  • Review

MeSH terms

  • Animals
  • Axons / physiology
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / physiology*
  • Cell Movement
  • Epilepsy / genetics
  • Epilepsy / metabolism
  • Humans
  • Ion Channel Gating
  • Mental Disorders / genetics
  • Mental Disorders / metabolism
  • Mutation
  • Nerve Degeneration / genetics
  • Nerve Degeneration / metabolism
  • Nervous System / embryology
  • Nervous System / growth & development
  • Nervous System / metabolism*
  • Neurites / physiology
  • Protein Subunits / genetics
  • Protein Subunits / physiology
  • Sodium Channels / genetics
  • Sodium Channels / physiology*

Substances

  • Cell Adhesion Molecules
  • Protein Subunits
  • Sodium Channels