Literature DB >> 12161074

Cardiac HCN channels: structure, function, and modulation.

Martin Biel1, Angela Schneider, Christian Wahl.   

Abstract

The hyperpolarization-activated cation current (termed I(f), I(h), or I(q)) plays a key role in the initiation and modulation of cardiac and neuronal pacemaker depolarizations. Recently, the hyperpolarization-activated cyclic nucleotide-gated (HCN) family of ion channel subunits has been identified by molecular cloning. When heterologously expressed, each of the four HCN subunits (HCN1-4) generates channels with the principal properties of native I(f), indicating that HCN channels are the molecular correlate of this current. This review describes the molecular and functional diversity of the HCN channel family. The structural determinants of channel activation, modulation, and ion permeation are discussed. The expression pattern of HCN channels in different heart regions is reviewed. Finally, the relationships between biophysical properties of cloned HCN channel types and native cardiac I(f) are explored.

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Year:  2002        PMID: 12161074     DOI: 10.1016/s1050-1738(02)00162-7

Source DB:  PubMed          Journal:  Trends Cardiovasc Med        ISSN: 1050-1738            Impact factor:   6.677


  66 in total

Review 1.  Regulation of recombinant and native hyperpolarization-activated cation channels.

Authors:  Samuel G A Frère; Mira Kuisle; Anita Lüthi
Journal:  Mol Neurobiol       Date:  2004-12       Impact factor: 5.590

2.  Thermodynamic properties of hyperpolarization-activated current (Ih) in a subgroup of primary sensory neurons.

Authors:  Florentina Pena; Bogdan Amuzescu; Emil Neaga; Maria-Luiza Flonta
Journal:  Exp Brain Res       Date:  2006-05-05       Impact factor: 1.972

3.  The enhancement of HCN channel instantaneous current facilitated by slow deactivation is regulated by intracellular chloride concentration.

Authors:  Pavel Mistrík; Alexander Pfeifer; Martin Biel
Journal:  Pflugers Arch       Date:  2006-05-20       Impact factor: 3.657

Review 4.  Embryological development of pacemaker hierarchy and membrane currents related to the function of the adult sinus node: implications for autonomic modulation of biopacemakers.

Authors:  Tobias Opthof
Journal:  Med Biol Eng Comput       Date:  2007-01-03       Impact factor: 2.602

Review 5.  Gene therapy to create biological pacemakers.

Authors:  Gerard J J Boink; Jurgen Seppen; Jacques M T de Bakker; Hanno L Tan
Journal:  Med Biol Eng Comput       Date:  2006-10-18       Impact factor: 2.602

6.  HCN4 provides a 'depolarization reserve' and is not required for heart rate acceleration in mice.

Authors:  Stefan Herrmann; Juliane Stieber; Georg Stöckl; Franz Hofmann; Andreas Ludwig
Journal:  EMBO J       Date:  2007-10-04       Impact factor: 11.598

7.  Single Ih channels in pyramidal neuron dendrites: properties, distribution, and impact on action potential output.

Authors:  Maarten H P Kole; Stefan Hallermann; Greg J Stuart
Journal:  J Neurosci       Date:  2006-02-08       Impact factor: 6.167

Review 8.  Biological pacemakers based on I(f).

Authors:  Michael R Rosen; Peter R Brink; Ira S Cohen; Richard B Robinson
Journal:  Med Biol Eng Comput       Date:  2006-05-31       Impact factor: 2.602

9.  Salt bridges and gating in the COOH-terminal region of HCN2 and CNGA1 channels.

Authors:  Kimberley B Craven; William N Zagotta
Journal:  J Gen Physiol       Date:  2004-12       Impact factor: 4.086

10.  State-dependent accessibility of the P-S6 linker of pacemaker (HCN) channels supports a dynamic pore-to-gate coupling model.

Authors:  Chung Wah Siu; Ezana M Azene; Ka Wing Au; Chu Pak Lau; Hung Fat Tse; Ronald A Li
Journal:  J Membr Biol       Date:  2009-07-17       Impact factor: 1.843

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