Associated changes in HCN2 and HCN4 transcripts and I(f) pacemaker current in myocytes

Biochim Biophys Acta. 2009 May;1788(5):1138-47. doi: 10.1016/j.bbamem.2009.02.011. Epub 2009 Feb 21.

Abstract

The time- and voltage-dependent inward current generated by the hyperpolarization-activated cyclic nucleotide-gated (HCN) channels contributes to the tissue-specific rhythmic activities in the brain and heart. Four isoforms (HCN1-HCN4) have been identified. Previous studies showed that different HCN isoforms may form functional heteromeric channels. We report here that when HCN2 and HCN4 mRNA were injected into Xenopus oocytes with various ratios of HCN2 over HCN4 at 1:1, 10:1, and 1:10, respectively, the resultant channels showed a depolarized current activation and significantly faster activation kinetics near the midpoint of activation compared with HCN4 homomeric channels. In adult rat myocytes overexpressing HCN4, there was an associated increase in HCN2 mRNA. In neonatal rat myocytes in which HCN2 was knocked down, there was also a simultaneous decrease in HCN4 mRNA. Coimmunoprecipitation experiments showed that HCN2 and HCN4 channel proteins can associate with each other in adult rat ventricles. Finally, in adult myocytes overexpressing HCN4, the hyperpolarization-activated inward current activation, I(f), was shifted to physiological voltages from non-physiological voltages, associated with faster activation kinetics. These data suggested that different ratios of HCN2 and HCN4 transcripts overlapping in different tissues also contribute to the tissue-specific properties of I(f).

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Base Sequence
  • Biophysical Phenomena
  • Cell Line
  • Cyclic Nucleotide-Gated Cation Channels / genetics*
  • Cyclic Nucleotide-Gated Cation Channels / metabolism
  • Electrophysiological Phenomena
  • Female
  • Humans
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • In Vitro Techniques
  • Ion Channels / antagonists & inhibitors
  • Ion Channels / genetics*
  • Ion Channels / metabolism
  • Membrane Potentials
  • Mice
  • Muscle Proteins / genetics*
  • Muscle Proteins / metabolism
  • Myocytes, Cardiac / metabolism*
  • Oocytes / metabolism
  • Patch-Clamp Techniques
  • Potassium Channels / genetics*
  • Potassium Channels / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics
  • Rats
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Xenopus laevis

Substances

  • Cyclic Nucleotide-Gated Cation Channels
  • HCN2 protein, human
  • HCN4 protein, human
  • HCN4 protein, rat
  • Hcn2 protein, mouse
  • Hcn2 protein, rat
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • Ion Channels
  • Muscle Proteins
  • Potassium Channels
  • RNA, Messenger
  • RNA, Small Interfering
  • Recombinant Proteins