The VAMP-associated protein VAPB is required for cardiac and neuronal pacemaker channel function

Research output: Contribution to journalArticlepeer-review

Authors

  • Nicole Silbernagel
  • Magdalena Walecki
  • Martin K -H Schafer
  • Mirjam Kessler
  • Mehrnoush Zobeiri
  • Susanne Rinné
  • Aytug K Kiper
  • Marlene A Komadowski
  • Kirsty S Vowinkel
  • Konstantin Wemhoner
  • Lisa Fortmüller
  • Marcus Schewe
  • Amalia M Dolga
  • Jelena Scekic-Zahirovic
  • Lina A Matschke
  • Carsten Culmsee
  • Thomas Baukrowitz
  • Laurent Monassier
  • Nina D Ullrich
  • Luc Dupuis
  • Steffen Just
  • Thomas Budde
  • Niels Decher

Colleges, School and Institutes

Abstract

Hyperpolarization-activated cyclic-nucleotide-gated (HCN) channels encode neuronal and cardiac pacemaker currents. The composition of pacemaker channel complexes in different tissues is poorly understood and the presence of additional HCN modulating subunits was speculated. Here we show that VAMP-Associated Protein B (VAPB), previously associated with a familial form of amyotrophic lateral sclerosis 8 (ALS8), is an essential HCN1 and HCN2 modulator. VAPB significantly increases HCN2 currents and surface expression and has a major influence on the dendritic neuronal distribution of HCN2. Severe cardiac bradycardias in VAPB-deficient zebrafish and VAPB-/- mice highlight that VAPB physiologically serves to increase cardiac pacemaker currents. An altered T-wave morphology observed in ECGs of VAPB-/- mice supports the recently proposed role of HCN channels for ventricular repolarization. The critical function of VAPB in native pacemaker channel complexes will be relevant for our understanding of cardiac arrhythmias, epilepsies, and provides an unexpected link between these diseases and ALS.

Details

Original languageEnglish
Pages (from-to)6159-6173
Number of pages15
JournalFASEB Journal
Volume32
Issue number11
Early online date7 Jun 2018
Publication statusPublished - Nov 2018

Keywords

  • ALS, HCN channels, cardiac arrhythmia