Literature DB >> 25442735

Insights into cardiac conduction system formation provided by HCN4 expression.

Xingqun Liang1, Sylvia M Evans2, Yunfu Sun3.   

Abstract

Specialized myocytes of the cardiac conduction system (CCS) are essential to coordinate sequential contraction of cardiac atria and ventricles. Anomalies of the CCS can result in lethal cardiac arrhythmias, including sick sinus syndrome and atrial or ventricular fibrillation. To develop future therapies and regenerative medicine aimed at cardiac arrhythmias, it is important to understand formation and function of distinct components of the CCS. Essential to this understanding is the development of CCS-specific markers. In this review, we briefly summarize available mouse models of CCS markers and focus on those involving the hyperpolarization cation-selective nucleotide-gated cation channel, HCN4, which selectively marks all components of the specialized CCS in adult heart. Recent studies have revealed, however, that HCN4 expression during development is highly dynamic in cardiac precursors. These studies have offered insights into the contributions of the first and second heart field to myocyte and conduction system lineages and suggested the timing of allocation of specific conduction system precursors during development. Altogether, they have highlighted the utility of HCN4 as a cell surface marker for distinct components of the CCS at distinct stages of development, which can be utilized to facilitate purification and characterization of CCS precursors in mouse and human model systems and pave the way for regenerative therapies.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 25442735      PMCID: PMC5544420          DOI: 10.1016/j.tcm.2014.08.009

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


  68 in total

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Review 2.  The second heart field.

Authors:  Robert G Kelly
Journal:  Curr Top Dev Biol       Date:  2012       Impact factor: 4.897

3.  Formation of the venous pole of the heart from an Nkx2-5-negative precursor population requires Tbx18.

Authors:  Vincent M Christoffels; Mathilda T M Mommersteeg; Mark-Oliver Trowe; Owen W J Prall; Corrie de Gier-de Vries; Alexandre T Soufan; Markus Bussen; Karin Schuster-Gossler; Richard P Harvey; Antoon F M Moorman; Andreas Kispert
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4.  Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.

Authors:  M C Sanguinetti; M E Curran; A Zou; J Shen; P S Spector; D L Atkinson; M T Keating
Journal:  Nature       Date:  1996-11-07       Impact factor: 49.962

5.  Location of pacemaker in chick embryo heart at the time of initiation of heartbeat.

Authors:  L H Van Mierop
Journal:  Am J Physiol       Date:  1967-02

6.  Complex genomic rearrangement in CCS-LacZ transgenic mice.

Authors:  Dina Myers Stroud; Bruce J Darrow; Sang Do Kim; Jie Zhang; Monique R M Jongbloed; Stacey Rentschler; Ivan P G Moskowitz; Jonathan Seidman; Glenn I Fishman
Journal:  Genesis       Date:  2007-02       Impact factor: 2.487

Review 7.  Establishment of the mouse ventricular conduction system.

Authors:  Lucile Miquerol; Sabrina Beyer; Robert G Kelly
Journal:  Cardiovasc Res       Date:  2011-03-08       Impact factor: 10.787

8.  The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart.

Authors:  Juliane Stieber; Stefan Herrmann; Susanne Feil; Jana Löster; Robert Feil; Martin Biel; Franz Hofmann; Andreas Ludwig
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-01       Impact factor: 11.205

9.  A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development.

Authors:  Ivan P G Moskowitz; Jae B Kim; Meredith L Moore; Cordula M Wolf; Michael A Peterson; Jay Shendure; Marcelo A Nobrega; Yoshifumi Yokota; Charles Berul; Seigo Izumo; J G Seidman; Christine E Seidman
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  11 in total

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Authors:  Xingqun Liang; Sylvia M Evans; Yunfu Sun
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4.  A mutant HCN4 channel in a family with bradycardia, left bundle branch block, and left ventricular noncompaction.

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Authors:  Michiko Watanabe; Andrew M Rollins; Luis Polo-Parada; Pei Ma; Shi Gu; Michael W Jenkins
Journal:  J Cardiovasc Dev Dis       Date:  2016-03-22

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Authors:  Emily Pitcairn; Hannah Harris; Justine Epiney; Vaibhav P Pai; Joan M Lemire; Bin Ye; Nian-Qing Shi; Michael Levin; Kelly A McLaughlin
Journal:  Commun Integr Biol       Date:  2017-05-10

7.  Segregation of Central Ventricular Conduction System Lineages in Early SMA+ Cardiomyocytes Occurs Prior to Heart Tube Formation.

Authors:  Caroline Choquet; Laetitia Marcadet; Sabrina Beyer; Robert G Kelly; Lucile Miquerol
Journal:  J Cardiovasc Dev Dis       Date:  2016-01-21

8.  Development of a Rat Model of Sick Sinus Syndrome Using Pinpoint Press Permeation.

Authors:  Hong-Bin Zhong; Ting-Jun Wang; Gui-Li Lian; Chang-Sheng Xu; Hua-Jun Wang; Liang-di Xie
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9.  Comprehensive Analysis and Co-Expression Network of mRNAs and lncRNAs in Pressure Overload-Induced Heart Failure.

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10.  ETV1 activates a rapid conduction transcriptional program in rodent and human cardiomyocytes.

Authors:  Akshay Shekhar; Xianming Lin; Bin Lin; Fang-Yu Liu; Jie Zhang; Alireza Khodadadi-Jamayran; Aristotelis Tsirigos; Lei Bu; Glenn I Fishman; David S Park
Journal:  Sci Rep       Date:  2018-07-02       Impact factor: 4.379

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