Referenced in: none

Automatically associated channels: HCN1 , HCN2

Title: Hyperpolarization-activated cyclic nucleotide-gated channels in pancreatic beta-cells.

Authors: Wasim El-Kholy, Patrick E MacDonald, Jocelyn Manning Fox, Alpana Bhattacharjee, Tian Xue, Xiaodong Gao, Yi Zhang, Juliane Stieber, Ronald A Li, Robert G Tsushima, Michael B Wheeler

Journal, date & volume: Mol. Endocrinol., 2007 Mar , 21, 753-64

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/17158221

Abstract
Hyperpolarization-activated cyclic nucleotide-modulated (HCN) channels mediate the pacemaker current (Ih or If) observed in electrically rhythmic cardiac and neuronal cells. Here we describe a hyperpolarization-activated time-dependent cationic current, beta-Ih, in pancreatic beta-cells. Transcripts for HCN1-4 were detected by RT-PCR and quantitative PCR in rat islets and MIN6 mouse insulinoma cells. beta-Ih in rat beta-cells and MIN6 cells displayed biophysical and pharmacological properties similar to those of HCN currents in cardiac and neuronal cells. Stimulation of cAMP production with forskolin/3-isobutyl-1-methylxanthine (50 microM) or dibutyryl-cAMP (1 mM) caused a significant rightward shift in the midpoint activation potential of beta-Ih, whereas expression of either specific small interfering (si)RNA against HCN2 (siHCN2b) or a dominant-negative HCN channel (HCN1-AAA) caused a near-complete inhibition of time-dependent beta-Ih. However, expression of siHCN2b in MIN6 cells had no affect on glucose-stimulated insulin secretion under normal or cAMP-stimulated conditions. Blocking beta-Ih in intact rat islets also did not affect membrane potential behavior at basal glucose concentrations. Taken together, our experiments provide the first evidence for functional expression of HCN channels in the pancreatic beta-cell.