Ion channel macromolecular complexes in cardiomyocytes: roles in sudden cardiac death

Circ Res. 2015 Jun 5;116(12):1971-88. doi: 10.1161/CIRCRESAHA.116.305017.

Abstract

The movement of ions across specific channels embedded on the membrane of individual cardiomyocytes is crucial for the generation and propagation of the cardiac electric impulse. Emerging evidence over the past 20 years strongly suggests that the normal electric function of the heart is the result of dynamic interactions of membrane ion channels working in an orchestrated fashion as part of complex molecular networks. Such networks work together with exquisite temporal precision to generate each action potential and contraction. Macromolecular complexes play crucial roles in transcription, translation, oligomerization, trafficking, membrane retention, glycosylation, post-translational modification, turnover, function, and degradation of all cardiac ion channels known to date. In addition, the accurate timing of each cardiac beat and contraction demands, a comparable precision on the assembly and organizations of sodium, calcium, and potassium channel complexes within specific subcellular microdomains, where physical proximity allows for prompt and efficient interaction. This review article, part of the Compendium on Sudden Cardiac Death, discusses the major issues related to the role of ion channel macromolecular assemblies in normal cardiac electric function and the mechanisms of arrhythmias leading to sudden cardiac death. It provides an idea of how these issues are being addressed in the laboratory and in the clinic, which important questions remain unanswered, and what future research will be needed to improve knowledge and advance therapy.

Keywords: arrhythmias, cardiac; death, sudden, cardiac; ion channels; multiprotein complexes.

Publication types

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

MeSH terms

  • Animals
  • Arrhythmias, Cardiac / etiology
  • Arrhythmias, Cardiac / genetics
  • Arrhythmias, Cardiac / physiopathology
  • Calcium Channels, L-Type / chemistry
  • Calcium Channels, L-Type / physiology
  • Cell Compartmentation
  • Channelopathies / complications*
  • Channelopathies / genetics
  • Channelopathies / physiopathology
  • Death, Sudden, Cardiac / etiology*
  • Disease Models, Animal
  • Heart Conduction System / physiopathology
  • Humans
  • Ion Channel Gating / drug effects
  • Ion Channel Gating / physiology
  • Ion Channels / chemistry
  • Ion Channels / drug effects
  • Ion Channels / physiology*
  • KATP Channels / chemistry
  • KATP Channels / physiology
  • Macromolecular Substances / chemistry*
  • Membrane Proteins / physiology
  • Mice
  • NAV1.5 Voltage-Gated Sodium Channel / chemistry
  • NAV1.5 Voltage-Gated Sodium Channel / physiology
  • Potassium Channels, Inwardly Rectifying / chemistry
  • Potassium Channels, Inwardly Rectifying / physiology
  • Protein Interaction Mapping
  • Protein Subunits

Substances

  • Calcium Channels, L-Type
  • Ion Channels
  • KATP Channels
  • KCNJ2 protein, human
  • L-type calcium channel alpha(1C)
  • Macromolecular Substances
  • Membrane Proteins
  • NAV1.5 Voltage-Gated Sodium Channel
  • Potassium Channels, Inwardly Rectifying
  • Protein Subunits
  • SCN5A protein, human