Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation

Circulation. 2005 Jul 26;112(4):471-81. doi: 10.1161/CIRCULATIONAHA.104.506857. Epub 2005 Jul 18.

Abstract

Background: Valvular heart disease (VHD), which often leads to atrial fibrillation (AF), and AF both cause ion-channel remodeling. We evaluated the ion-channel gene expression profile of VHD patients, in permanent AF (AF-VHD) or in sinus rhythm (SR-VHD), in comparison with patients without AF or VHD, respectively.

Methods and results: We used microarrays containing probes for human ion-channel and Ca2+-regulator genes to quantify mRNA expression in atrial tissues from 7 SR-VHD patients and 11 AF-VHD patients relative to 11 control patients in SR without structural heart disease (SR-CAD). From the data set, we selected for detailed analysis 59 transcripts expressed in the human heart. SR-VHD patients differentially expressed 24/59 ion-channel and Ca2+-regulator transcripts. There was significant overlap between VHD groups, with 66% of genes altered in SR-VHD patients being similarly modified in AF-VHD. Statistical differences between the AF- and SR-VHD groups identified the specific molecular portrait of AF, which involved 12 genes that were further confirmed by real-time reverse transcription-polymerase chain reaction. For example, phospholamban, the beta-subunit MinK (KCNE1) and MIRP2 (KCNE3), and the 2-pore potassium channel TWIK-1 were upregulated in AF-VHD compared with SR-VHD, whereas the T-type calcium-channel Cav3.1 and the transient-outward potassium channel Kv4.3 were downregulated. Two-way hierarchical clustering separated SR-VHD from AF-VHD patients. AF-related changes in L-type Ca2+-current and inward-rectifier current were confirmed at protein and functional levels. Finally, for 13 selected genes, SR restoration reversed ion-channel remodeling.

Conclusions: VHD extensively remodels cardiac ion-channel and transporter expression, and AF alters ion-channel expression in VHD patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Atrial Fibrillation / metabolism*
  • Blotting, Western
  • Calcium Channels, L-Type / genetics
  • Connexins / genetics
  • Gap Junction alpha-5 Protein
  • Gene Expression Profiling
  • Heart Atria / metabolism*
  • Heart Valve Diseases / metabolism*
  • Humans
  • Ion Channels / genetics*
  • Membrane Transport Proteins / genetics
  • Potassium Channels, Inwardly Rectifying / genetics
  • Protein Subunits
  • Reverse Transcriptase Polymerase Chain Reaction
  • Shal Potassium Channels / genetics

Substances

  • Calcium Channels, L-Type
  • Connexins
  • Ion Channels
  • KCNJ2 protein, human
  • L-type calcium channel alpha(1C)
  • Membrane Transport Proteins
  • Potassium Channels, Inwardly Rectifying
  • Protein Subunits
  • Shal Potassium Channels